Trial Outcomes & Findings for Highly Conformal, Hypofractionated, Focally Dose Escalated Post-Prostatectomy Radiotherapy (NCT NCT03388619)
NCT ID: NCT03388619
Last Updated: 2026-08-28
Results Overview
Maximum tolerated dose (MTD) of image guided hypofractionated, focally dose escalated post-prostatectomy radiation is defined as the dose level at which no more than 1 of up to 6 participants experience dose limiting toxicity (DLT) during the DLT period, and the dose below that at which at least 2 (of ≤6) participants have DLT as a result of treatment. A DLT is defined as any of the following: Grade 3 rectal, small bowel, or urinary toxicity that does not resolve to Grade 2 or less within 4 days with appropriate medical management. Other grade 3 in-field toxicities attributable to radiation that does not resolve to Grade 2 or less within 4 days with appropriate medical management. And delays of more than one week in completing radiation treatment due to toxicity.
COMPLETED
PHASE1
30 participants
3 weeks after radiation
2026-08-28
Participant Flow
Participant milestones
| Measure |
LEVEL 1/ COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 20 Fractions
LEVEL 1/ COHORT 1: Recurrent tumor visible; prostate bed with integrated boost. 20 fractions: Dose to prostate bed 45.8 Gray (Gy) in 2.29 Gy fractions; Dose to tumor 60.4 Gy in 3.02 Gy fractions.
|
LEVEL 2/ COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 15 Fractions
LEVEL 2/ COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 15 fractions: Dose to prostate bed 41.85 Gray (Gy) in 2.79 Gy fractions; Dose to tumor 54.6 Gy in 3.64 Gy fractions.
|
LEVEL 3/ COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 10 Fractions
LEVEL 3/ COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
LEVEL 1/ COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 20 Fractions
LEVEL 1/ COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 20 fractions: Dose to prostate bed 56.4 Gray (Gy) in 2.82 Gy fractions.
|
LEVEL 2/ COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 15 Fractions
LEVEL 2/ COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 15 fractions: Dose to prostate bed 51.2 Gray (Gy) in 3.41 Gy fractions.
|
LEVEL 3/ COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 10 Fractions
LEVEL 3/ COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
|---|---|---|---|---|---|---|
|
Overall Study
STARTED
|
3
|
3
|
9
|
3
|
3
|
9
|
|
Overall Study
Follow-up period completed.
|
3
|
3
|
5
|
3
|
3
|
8
|
|
Overall Study
COMPLETED
|
3
|
3
|
9
|
3
|
3
|
9
|
|
Overall Study
NOT COMPLETED
|
0
|
0
|
0
|
0
|
0
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Highly Conformal, Hypofractionated, Focally Dose Escalated Post-Prostatectomy Radiotherapy
Baseline characteristics by cohort
| Measure |
LEVEL 1/ COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 20 Fractions
n=3 Participants
LEVEL 1/ COHORT 1: Recurrent tumor visible; prostate bed with integrated boost. 20 fractions: Dose to prostate bed 45.8 Gray (Gy) in 2.29 Gy fractions; Dose to tumor 60.4 Gy in 3.02 Gy fractions.
|
LEVEL 2/ COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 15 Fractions
n=3 Participants
LEVEL 2/ COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 15 fractions: Dose to prostate bed 41.85 Gray (Gy) in 2.79 Gy fractions; Dose to tumor 54.6 Gy in 3.64 Gy fractions.
|
LEVEL 3/ COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 10 Fractions
n=9 Participants
LEVEL 3/ COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
LEVEL 1/ COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 20 Fractions
n=3 Participants
LEVEL 1/ COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 20 fractions: Dose to prostate bed 56.4 Gray (Gy) in 2.82 Gy fractions.
|
LEVEL 2/ COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 15 Fractions
n=3 Participants
LEVEL 2/ COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 15 fractions: Dose to prostate bed 51.2 Gray (Gy) in 3.41 Gy fractions.
|
LEVEL 3/ COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 10 Fractions
n=9 Participants
LEVEL 3/ COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
Total
n=30 Participants
Total of all reporting groups
|
|---|---|---|---|---|---|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=31 Participants
|
0 Participants
n=49 Participants
|
0 Participants
n=80 Participants
|
0 Participants
n=29 Participants
|
0 Participants
n=106 Participants
|
0 Participants
n=6 Participants
|
0 Participants
n=6 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
1 Participants
n=31 Participants
|
1 Participants
n=49 Participants
|
3 Participants
n=80 Participants
|
1 Participants
n=29 Participants
|
0 Participants
n=106 Participants
|
4 Participants
n=6 Participants
|
10 Participants
n=6 Participants
|
|
Age, Categorical
>=65 years
|
2 Participants
n=31 Participants
|
2 Participants
n=49 Participants
|
6 Participants
n=80 Participants
|
2 Participants
n=29 Participants
|
3 Participants
n=106 Participants
|
5 Participants
n=6 Participants
|
20 Participants
n=6 Participants
|
|
Age, Continuous
|
65.63 years
STANDARD_DEVIATION 7.35 • n=31 Participants
|
67.4 years
STANDARD_DEVIATION 3.02 • n=49 Participants
|
67.04 years
STANDARD_DEVIATION 7.51 • n=80 Participants
|
67.63 years
STANDARD_DEVIATION 9.87 • n=29 Participants
|
70.87 years
STANDARD_DEVIATION 1.61 • n=106 Participants
|
64.32 years
STANDARD_DEVIATION 10.4 • n=6 Participants
|
66.56 years
STANDARD_DEVIATION 7.78 • n=6 Participants
|
|
Sex: Female, Male
Female
|
0 Participants
n=31 Participants
|
0 Participants
n=49 Participants
|
0 Participants
n=80 Participants
|
0 Participants
n=29 Participants
|
0 Participants
n=106 Participants
|
0 Participants
n=6 Participants
|
0 Participants
n=6 Participants
|
|
Sex: Female, Male
Male
|
3 Participants
n=31 Participants
|
3 Participants
n=49 Participants
|
9 Participants
n=80 Participants
|
3 Participants
n=29 Participants
|
3 Participants
n=106 Participants
|
9 Participants
n=6 Participants
|
30 Participants
n=6 Participants
|
|
Ethnicity (NIH/OMB)
Hispanic or Latino
|
0 Participants
n=31 Participants
|
0 Participants
n=49 Participants
|
0 Participants
n=80 Participants
|
0 Participants
n=29 Participants
|
0 Participants
n=106 Participants
|
1 Participants
n=6 Participants
|
1 Participants
n=6 Participants
|
|
Ethnicity (NIH/OMB)
Not Hispanic or Latino
|
3 Participants
n=31 Participants
|
3 Participants
n=49 Participants
|
9 Participants
n=80 Participants
|
3 Participants
n=29 Participants
|
3 Participants
n=106 Participants
|
8 Participants
n=6 Participants
|
29 Participants
n=6 Participants
|
|
Ethnicity (NIH/OMB)
Unknown or Not Reported
|
0 Participants
n=31 Participants
|
0 Participants
n=49 Participants
|
0 Participants
n=80 Participants
|
0 Participants
n=29 Participants
|
0 Participants
n=106 Participants
|
0 Participants
n=6 Participants
|
0 Participants
n=6 Participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
0 Participants
n=31 Participants
|
0 Participants
n=49 Participants
|
0 Participants
n=80 Participants
|
0 Participants
n=29 Participants
|
0 Participants
n=106 Participants
|
0 Participants
n=6 Participants
|
0 Participants
n=6 Participants
|
|
Race (NIH/OMB)
Asian
|
0 Participants
n=31 Participants
|
0 Participants
n=49 Participants
|
0 Participants
n=80 Participants
|
0 Participants
n=29 Participants
|
0 Participants
n=106 Participants
|
0 Participants
n=6 Participants
|
0 Participants
n=6 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=31 Participants
|
0 Participants
n=49 Participants
|
0 Participants
n=80 Participants
|
0 Participants
n=29 Participants
|
0 Participants
n=106 Participants
|
0 Participants
n=6 Participants
|
0 Participants
n=6 Participants
|
|
Race (NIH/OMB)
Black or African American
|
2 Participants
n=31 Participants
|
0 Participants
n=49 Participants
|
3 Participants
n=80 Participants
|
0 Participants
n=29 Participants
|
1 Participants
n=106 Participants
|
2 Participants
n=6 Participants
|
8 Participants
n=6 Participants
|
|
Race (NIH/OMB)
White
|
1 Participants
n=31 Participants
|
3 Participants
n=49 Participants
|
6 Participants
n=80 Participants
|
3 Participants
n=29 Participants
|
2 Participants
n=106 Participants
|
7 Participants
n=6 Participants
|
22 Participants
n=6 Participants
|
|
Race (NIH/OMB)
More than one race
|
0 Participants
n=31 Participants
|
0 Participants
n=49 Participants
|
0 Participants
n=80 Participants
|
0 Participants
n=29 Participants
|
0 Participants
n=106 Participants
|
0 Participants
n=6 Participants
|
0 Participants
n=6 Participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
0 Participants
n=31 Participants
|
0 Participants
n=49 Participants
|
0 Participants
n=80 Participants
|
0 Participants
n=29 Participants
|
0 Participants
n=106 Participants
|
0 Participants
n=6 Participants
|
0 Participants
n=6 Participants
|
|
Region of Enrollment
United States
|
3 participants
n=31 Participants
|
3 participants
n=49 Participants
|
9 participants
n=80 Participants
|
3 participants
n=29 Participants
|
3 participants
n=106 Participants
|
9 participants
n=6 Participants
|
30 participants
n=6 Participants
|
PRIMARY outcome
Timeframe: 3 weeks after radiationPopulation: 12/30 expansion group participants (6 in Recurrent Tumor Visible: Level 3 Cohort 1, and Recurrent Tumor NOT Visible: Level 3 Cohort 2) were not assessed for MTD and included in the analysis.
Maximum tolerated dose (MTD) of image guided hypofractionated, focally dose escalated post-prostatectomy radiation is defined as the dose level at which no more than 1 of up to 6 participants experience dose limiting toxicity (DLT) during the DLT period, and the dose below that at which at least 2 (of ≤6) participants have DLT as a result of treatment. A DLT is defined as any of the following: Grade 3 rectal, small bowel, or urinary toxicity that does not resolve to Grade 2 or less within 4 days with appropriate medical management. Other grade 3 in-field toxicities attributable to radiation that does not resolve to Grade 2 or less within 4 days with appropriate medical management. And delays of more than one week in completing radiation treatment due to toxicity.
Outcome measures
| Measure |
All Participants With Recurrent Tumor Visible
n=9 Participants
All participants with recurrent tumor visible assessed for MTD.
Level 1 Cohort 1, Level 2 Cohort 1, and Level 3 Cohort 1:
Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
All Participants With Recurrent Tumor NOT Visible
n=9 Participants
All participants with recurrent tumor NOT visible assessed for MTD.
Level 1 Cohort 2, Level 2 Cohort 2, and Level 3 Cohort 2:
Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
LEVEL 3/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 10 Fractions
LEVEL 3/COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
LEVEL 1/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 20 Fractions
LEVEL 1/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 20 fractions: Dose to prostate bed 56.4 Gray (Gy) in 2.82 Gy fractions.
|
LEVEL 2/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 15 Fractions
LEVEL 2/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 15 fractions: Dose to prostate bed 51.2 Gray (Gy) in 3.41 Gy fractions.
|
LEVEL 3/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 10 Fractions
LEVEL 3/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
|---|---|---|---|---|---|---|
|
Maximum Tolerated Dose (MTD) of Radiation Dose to Prostate Bed and Dose to Tumor Reported in Gray (Gy)
Dose to prostate bed
|
36.4 Gray (Gy)
|
44.2 Gray (Gy)
|
—
|
—
|
—
|
—
|
|
Maximum Tolerated Dose (MTD) of Radiation Dose to Prostate Bed and Dose to Tumor Reported in Gray (Gy)
Dose to tumor
|
47.1 Gray (Gy)
|
—
|
—
|
—
|
—
|
—
|
PRIMARY outcome
Timeframe: 3 weeks after radiationPopulation: 12/30 expansion group participants (6 in Recurrent Tumor Visible: Level 3 Cohort 1, and Recurrent Tumor NOT Visible: Level 3 Cohort 2) were not assessed for MTD and included in the analysis.
Maximum tolerated dose (MTD) of image guided hypofractionated, focally dose escalated post-prostatectomy radiation is defined as the dose level at which no more than 1 of up to 6 participants experience dose limiting toxicity (DLT) during the DLT period, and the dose below that at which at least 2 (of ≤6) participants have DLT as a result of treatment. A DLT is defined as any of the following: Grade 3 rectal, small bowel, or urinary toxicity that does not resolve to Grade 2 or less within 4 days with appropriate medical management. Other grade 3 in-field toxicities attributable to radiation that does not resolve to Grade 2 or less within 4 days with appropriate medical management. And delays of more than one week in completing radiation treatment due to toxicity.
Outcome measures
| Measure |
All Participants With Recurrent Tumor Visible
n=9 Participants
All participants with recurrent tumor visible assessed for MTD.
Level 1 Cohort 1, Level 2 Cohort 1, and Level 3 Cohort 1:
Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
All Participants With Recurrent Tumor NOT Visible
n=9 Participants
All participants with recurrent tumor NOT visible assessed for MTD.
Level 1 Cohort 2, Level 2 Cohort 2, and Level 3 Cohort 2:
Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
LEVEL 3/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 10 Fractions
LEVEL 3/COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
LEVEL 1/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 20 Fractions
LEVEL 1/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 20 fractions: Dose to prostate bed 56.4 Gray (Gy) in 2.82 Gy fractions.
|
LEVEL 2/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 15 Fractions
LEVEL 2/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 15 fractions: Dose to prostate bed 51.2 Gray (Gy) in 3.41 Gy fractions.
|
LEVEL 3/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 10 Fractions
LEVEL 3/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
|---|---|---|---|---|---|---|
|
Maximum Tolerated Dose (MTD) of Radiation Dose to Prostate Bed and Dose to Tumor Reported in Fractions
Dose to prostate bed
|
3.64 Fractions
|
4.42 Fractions
|
—
|
—
|
—
|
—
|
|
Maximum Tolerated Dose (MTD) of Radiation Dose to Prostate Bed and Dose to Tumor Reported in Fractions
Dose to tumor
|
4.71 Fractions
|
—
|
—
|
—
|
—
|
—
|
SECONDARY outcome
Timeframe: 1 and 2 years after treatmentPopulation: Participants that complete at least one post-treatment PSA are evaluable for this outcome. Secondary endpoints were analyzed by treatment arm rather than by individual dose level because the study was designed as a Phase I dose-escalation trial, with the primary objective of establishing the maximum tolerated dose. Any apparent differences between dose levels would be driven by random variation rather than meaningful treatment effects and could be misinterpreted.
bPFS is defined as the percent of participants without evidence of (prostate-specific antigen) PSA progression or death. PSA progression (also known as biochemical failure) is defined based on elevation of PSA above 0.1 ng/dL. Kaplan-Meier survival analysis will be used to report bPFS.
Outcome measures
| Measure |
All Participants With Recurrent Tumor Visible
n=9 Participants
All participants with recurrent tumor visible assessed for MTD.
Level 1 Cohort 1, Level 2 Cohort 1, and Level 3 Cohort 1:
Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
All Participants With Recurrent Tumor NOT Visible
n=9 Participants
All participants with recurrent tumor NOT visible assessed for MTD.
Level 1 Cohort 2, Level 2 Cohort 2, and Level 3 Cohort 2:
Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
LEVEL 3/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 10 Fractions
LEVEL 3/COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
LEVEL 1/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 20 Fractions
LEVEL 1/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 20 fractions: Dose to prostate bed 56.4 Gray (Gy) in 2.82 Gy fractions.
|
LEVEL 2/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 15 Fractions
LEVEL 2/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 15 fractions: Dose to prostate bed 51.2 Gray (Gy) in 3.41 Gy fractions.
|
LEVEL 3/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 10 Fractions
LEVEL 3/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
|---|---|---|---|---|---|---|
|
Biochemical Progression Free Survival (bPFS)
1 year after treatment
|
97 Percent of participants
|
100 Percent of participants
|
—
|
—
|
—
|
—
|
|
Biochemical Progression Free Survival (bPFS)
2 years after treatment
|
93 Percent of participants
|
100 Percent of participants
|
—
|
—
|
—
|
—
|
SECONDARY outcome
Timeframe: Baseline compared to 24 months after treatmentPopulation: Secondary endpoints were analyzed by treatment arm rather than by individual dose level because the study was designed as a Phase I dose-escalation trial, with the primary objective of establishing the maximum tolerated dose. Any apparent differences between dose levels would be driven by random variation rather than meaningful treatment effects and could be misinterpreted.
Changes before and after treatment with prostate bed radiation in participant reported outcomes (Sexual Health Inventory for Men (SHIM). The QOL scores will be summarized at baseline and after treatment. Linear mixed effects model will be used to model quality of life scores at baseline and during and after treatment in which random intercept and random slope are used to account for participant-specific trajectory of QOL scores. The SHIM is a 5-question quiz used to identify erectile dysfunction and assess its severity. The composite score is generated by adding the score for each question. The total score can range from 1-25. Higer values represent better erectile function.
Outcome measures
| Measure |
All Participants With Recurrent Tumor Visible
n=9 Participants
All participants with recurrent tumor visible assessed for MTD.
Level 1 Cohort 1, Level 2 Cohort 1, and Level 3 Cohort 1:
Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
All Participants With Recurrent Tumor NOT Visible
n=9 Participants
All participants with recurrent tumor NOT visible assessed for MTD.
Level 1 Cohort 2, Level 2 Cohort 2, and Level 3 Cohort 2:
Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
LEVEL 3/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 10 Fractions
LEVEL 3/COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
LEVEL 1/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 20 Fractions
LEVEL 1/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 20 fractions: Dose to prostate bed 56.4 Gray (Gy) in 2.82 Gy fractions.
|
LEVEL 2/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 15 Fractions
LEVEL 2/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 15 fractions: Dose to prostate bed 51.2 Gray (Gy) in 3.41 Gy fractions.
|
LEVEL 3/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 10 Fractions
LEVEL 3/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
|---|---|---|---|---|---|---|
|
Changes in Erectile Dysfunction QOL Scores During and After Treatment Measured by the Sexual Health Inventory for Men (SHIM)
Baseline
|
10.0 Score on a scale
Standard Deviation 8.3
|
5.9 Score on a scale
Standard Deviation 7.2
|
—
|
—
|
—
|
—
|
|
Changes in Erectile Dysfunction QOL Scores During and After Treatment Measured by the Sexual Health Inventory for Men (SHIM)
After treatment
|
7.9 Score on a scale
Standard Deviation 7.0
|
2.2 Score on a scale
Standard Deviation 2.3
|
—
|
—
|
—
|
—
|
SECONDARY outcome
Timeframe: Baseline compared to 24 months after treatmentPopulation: Secondary endpoints were analyzed by treatment arm rather than by individual dose level because the study was designed as a Phase I dose-escalation trial, with the primary objective of establishing the maximum tolerated dose. Any apparent differences between dose levels would be driven by random variation rather than meaningful treatment effects and could be misinterpreted.
Changes of QOL scores during and after treatment with prostate bed radiation in American Urologic Association (AUA) Symptom Index. The QOL scores will be summarized at baseline and for each visit. Linear mixed effects model will be used to model quality of life scores at baseline and during and after treatment in which random intercept and random slope are used to account for participant-specific trajectory of QOL scores. The AUA Symptom Index is a 7-question quiz used to identify urinary symptoms and assess severity. Each question is scored based on the frequency of different urinary symptoms. The composite score is generated by adding the score for each question. The total score can range from 0-35. Lower values represent less symptoms.
Outcome measures
| Measure |
All Participants With Recurrent Tumor Visible
n=9 Participants
All participants with recurrent tumor visible assessed for MTD.
Level 1 Cohort 1, Level 2 Cohort 1, and Level 3 Cohort 1:
Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
All Participants With Recurrent Tumor NOT Visible
n=9 Participants
All participants with recurrent tumor NOT visible assessed for MTD.
Level 1 Cohort 2, Level 2 Cohort 2, and Level 3 Cohort 2:
Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
LEVEL 3/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 10 Fractions
LEVEL 3/COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
LEVEL 1/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 20 Fractions
LEVEL 1/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 20 fractions: Dose to prostate bed 56.4 Gray (Gy) in 2.82 Gy fractions.
|
LEVEL 2/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 15 Fractions
LEVEL 2/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 15 fractions: Dose to prostate bed 51.2 Gray (Gy) in 3.41 Gy fractions.
|
LEVEL 3/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 10 Fractions
LEVEL 3/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
|---|---|---|---|---|---|---|
|
Changes of American Urologic Association (AUA) Symptom Index Quality of Life (QOL) Scores During and After Treatment
Baseline
|
8.8 Score on a scale
Standard Deviation 4.6
|
7.6 Score on a scale
Standard Deviation 5.3
|
—
|
—
|
—
|
—
|
|
Changes of American Urologic Association (AUA) Symptom Index Quality of Life (QOL) Scores During and After Treatment
After treatment
|
7.4 Score on a scale
Standard Deviation 5.2
|
11.9 Score on a scale
Standard Deviation 8.9
|
—
|
—
|
—
|
—
|
SECONDARY outcome
Timeframe: Baseline compared to 24 months after treatmentPopulation: Secondary endpoints were analyzed by treatment arm rather than by individual dose level because the study was designed as a Phase I dose-escalation trial, with the primary objective of establishing the maximum tolerated dose. Any apparent differences between dose levels would be driven by random variation rather than meaningful treatment effects and could be misinterpreted.
Changes of QOL scores during and after treatment of focally dose escalated prostate stereotactic body radiation therapy on participant(pt) reported outcomes, EPIC-26 in pts previously treated with radiotherapy. The QOL scores will be summarized at baseline and for each visit. Linear mixed effects model will be used to model QOL scores at baseline and during and after treatment in which random intercept and random slope are used to account for pt-specific trajectory of QOL scores. The EPIC-26 is a shortened, validated questionnaire used to assess health related QOL in individuals with prostate cancer. EPIC26 measures sexual function, bowel function, hormone therapy side effects, urinary incontinence, and urinary irritative symptoms. The survey has 26 individual items that have 4 to 5 response options that reflect a range of function from poor to excellent. EPIC26 uses a Likert scale for each item, and scores are transformed to a 0-100 scale, with higher scores indicating better HRQOL.
Outcome measures
| Measure |
All Participants With Recurrent Tumor Visible
n=9 Participants
All participants with recurrent tumor visible assessed for MTD.
Level 1 Cohort 1, Level 2 Cohort 1, and Level 3 Cohort 1:
Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
All Participants With Recurrent Tumor NOT Visible
n=9 Participants
All participants with recurrent tumor NOT visible assessed for MTD.
Level 1 Cohort 2, Level 2 Cohort 2, and Level 3 Cohort 2:
Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
LEVEL 3/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 10 Fractions
LEVEL 3/COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
LEVEL 1/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 20 Fractions
LEVEL 1/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 20 fractions: Dose to prostate bed 56.4 Gray (Gy) in 2.82 Gy fractions.
|
LEVEL 2/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 15 Fractions
LEVEL 2/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 15 fractions: Dose to prostate bed 51.2 Gray (Gy) in 3.41 Gy fractions.
|
LEVEL 3/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 10 Fractions
LEVEL 3/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
|---|---|---|---|---|---|---|
|
Changes of Expanded Prostate Cancer Index Composite (EPIC-26) Quality of Life (QOL) Scores During and After Treatment
Baseline Urinary Incontinence
|
73.5 Score on a scale
Standard Deviation 25.6
|
63.4 Score on a scale
Standard Deviation 24.9
|
—
|
—
|
—
|
—
|
|
Changes of Expanded Prostate Cancer Index Composite (EPIC-26) Quality of Life (QOL) Scores During and After Treatment
After treatment Urinary Incontinence
|
67.9 Score on a scale
Standard Deviation 25.8
|
36.4 Score on a scale
Standard Deviation 31.6
|
—
|
—
|
—
|
—
|
|
Changes of Expanded Prostate Cancer Index Composite (EPIC-26) Quality of Life (QOL) Scores During and After Treatment
Baseline Urinary Irritative/Obstructive
|
90 Score on a scale
Standard Deviation 6.6
|
89.6 Score on a scale
Standard Deviation 9.0
|
—
|
—
|
—
|
—
|
|
Changes of Expanded Prostate Cancer Index Composite (EPIC-26) Quality of Life (QOL) Scores During and After Treatment
After Treatment Urinary Irritative/Obstructive
|
87.9 Score on a scale
Standard Deviation 12.1
|
78.4 Score on a scale
Standard Deviation 16.3
|
—
|
—
|
—
|
—
|
|
Changes of Expanded Prostate Cancer Index Composite (EPIC-26) Quality of Life (QOL) Scores During and After Treatment
Baseline Bowel
|
95.3 Score on a scale
Standard Deviation 8.3
|
97.8 Score on a scale
Standard Deviation 4.1
|
—
|
—
|
—
|
—
|
|
Changes of Expanded Prostate Cancer Index Composite (EPIC-26) Quality of Life (QOL) Scores During and After Treatment
After Treatment Bowel
|
94.9 Score on a scale
Standard Deviation 6.2
|
84.5 Score on a scale
Standard Deviation 21.8
|
—
|
—
|
—
|
—
|
|
Changes of Expanded Prostate Cancer Index Composite (EPIC-26) Quality of Life (QOL) Scores During and After Treatment
Baseline Sexual
|
40.3 Score on a scale
Standard Deviation 28.4
|
30.1 Score on a scale
Standard Deviation 27.1
|
—
|
—
|
—
|
—
|
|
Changes of Expanded Prostate Cancer Index Composite (EPIC-26) Quality of Life (QOL) Scores During and After Treatment
After treatment Sexual
|
31.0 Score on a scale
Standard Deviation 21.7
|
15.9 Score on a scale
Standard Deviation 21.4
|
—
|
—
|
—
|
—
|
SECONDARY outcome
Timeframe: 3 weeks after radiationGrade 2-5 serious and/or non-serious adverse events attributable to protocol treatment. A non-serious adverse event is any untoward medical occurrence. A serious adverse event is an adverse event or suspected adverse reaction that results in death, a life-threatening adverse drug experience, hospitalization, disruption of the ability to conduct normal life functions, congenital anomaly/birth defect or important medical events that jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the previous outcomes mentioned. Grade 2 is moderate. Grade 3 is serious. Grade 4 is life-threatening. And Grade 5 is death related to adverse event.
Outcome measures
| Measure |
All Participants With Recurrent Tumor Visible
n=3 Participants
All participants with recurrent tumor visible assessed for MTD.
Level 1 Cohort 1, Level 2 Cohort 1, and Level 3 Cohort 1:
Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
All Participants With Recurrent Tumor NOT Visible
n=3 Participants
All participants with recurrent tumor NOT visible assessed for MTD.
Level 1 Cohort 2, Level 2 Cohort 2, and Level 3 Cohort 2:
Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
LEVEL 3/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 10 Fractions
n=9 Participants
LEVEL 3/COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
LEVEL 1/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 20 Fractions
n=3 Participants
LEVEL 1/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 20 fractions: Dose to prostate bed 56.4 Gray (Gy) in 2.82 Gy fractions.
|
LEVEL 2/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 15 Fractions
n=3 Participants
LEVEL 2/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 15 fractions: Dose to prostate bed 51.2 Gray (Gy) in 3.41 Gy fractions.
|
LEVEL 3/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 10 Fractions
n=9 Participants
LEVEL 3/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
|---|---|---|---|---|---|---|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Possibly Related Urinary tract obstruction
|
0 adverse events
|
1 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Probably Related Rectal hemorrhage
|
0 adverse events
|
0 adverse events
|
1 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Probably Related Urinary urgency
|
0 adverse events
|
1 adverse events
|
0 adverse events
|
0 adverse events
|
1 adverse events
|
0 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 3 Probably Related Cystitis noninfective
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
1 adverse events
|
0 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Possibly Related Hemorrhoids
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
2 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Possibly Related Diarrhea
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
1 adverse events
|
0 adverse events
|
1 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Possibly Related Skin infection
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
1 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Probably Related - Urinary urgency
|
1 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
1 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Probably Related Proctitis
|
0 adverse events
|
2 adverse events
|
3 adverse events
|
0 adverse events
|
2 adverse events
|
6 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Probably Related Diarrhea
|
0 adverse events
|
0 adverse events
|
1 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Probably Related Flatulence
|
0 adverse events
|
0 adverse events
|
2 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Probably Related Hemorrhoids
|
0 adverse events
|
1 adverse events
|
1 adverse events
|
0 adverse events
|
0 adverse events
|
5 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Probably Related Cystitis noninfective
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
1 adverse events
|
1 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Probably Related Urinary frequency
|
0 adverse events
|
0 adverse events
|
1 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Probably Related Urinary incontinence
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
1 adverse events
|
0 adverse events
|
0 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 3 Probably Related Proctitis
|
0 adverse events
|
0 adverse events
|
1 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 3 Probably Related Urinary incontinence
|
0 adverse events
|
1 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Definitely Related Flatulence
|
0 adverse events
|
0 adverse events
|
1 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2-5 Serious
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Unlikely Related - Skin and subcutaneous tissue disorders - Other, specify
|
1 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Unlikely Related Hemorrhoids
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
1 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Unlikely Related Testicular pain
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
1 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Unlikely Related Testicular disorder
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
1 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Possibly Related Flatulence
|
0 adverse events
|
0 adverse events
|
1 adverse events
|
0 adverse events
|
0 adverse events
|
0 adverse events
|
|
Grade 2-5 Serious and/or Non-serious Adverse Events Unlikely, Probably, Possibly and Definitely Attributable to Research
Grade 2 Definitely Related Proctitis
|
0 adverse events
|
0 adverse events
|
3 adverse events
|
0 adverse events
|
0 adverse events
|
4 adverse events
|
OTHER_PRE_SPECIFIED outcome
Timeframe: Date treatment consent signed to date off study, an average of 25 monthsHere is the number of participants with serious and/or non-serious adverse events assessed by the Common Terminology Criteria for Adverse Events (CTCAE v4.0). A non-serious adverse event is any untoward medical occurrence. A serious adverse event is an adverse event or suspected adverse reaction that results in death, a life-threatening adverse drug experience, hospitalization, disruption of the ability to conduct normal life functions, congenital anomaly/birth defect or important medical events that jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the previous outcomes mentioned.
Outcome measures
| Measure |
All Participants With Recurrent Tumor Visible
n=3 Participants
All participants with recurrent tumor visible assessed for MTD.
Level 1 Cohort 1, Level 2 Cohort 1, and Level 3 Cohort 1:
Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
All Participants With Recurrent Tumor NOT Visible
n=3 Participants
All participants with recurrent tumor NOT visible assessed for MTD.
Level 1 Cohort 2, Level 2 Cohort 2, and Level 3 Cohort 2:
Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
LEVEL 3/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 10 Fractions
n=9 Participants
LEVEL 3/COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
LEVEL 1/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 20 Fractions
n=3 Participants
LEVEL 1/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 20 fractions: Dose to prostate bed 56.4 Gray (Gy) in 2.82 Gy fractions.
|
LEVEL 2/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 15 Fractions
n=3 Participants
LEVEL 2/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 15 fractions: Dose to prostate bed 51.2 Gray (Gy) in 3.41 Gy fractions.
|
LEVEL 3/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 10 Fractions
n=9 Participants
LEVEL 3/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
|---|---|---|---|---|---|---|
|
Number of Participants With Serious and/or Non-serious Adverse Events Assessed by the Common Terminology Criteria for Adverse Events (CTCAE v4.0)
|
3 Participants
|
3 Participants
|
8 Participants
|
3 Participants
|
3 Participants
|
9 Participants
|
OTHER_PRE_SPECIFIED outcome
Timeframe: 3 weeks after radiationA DLT is defined as any of the following: Grade 3 rectal, small bowel, or urinary toxicity that does not resolve to Grade 2 or less within 4 days with appropriate medical management. Other grade 3 in-field toxicities attributable to radiation that does not resolve to Grade 2 or less within 4 days with appropriate medical management. And delays of more than one week in completing radiation treatment due to toxicity.
Outcome measures
| Measure |
All Participants With Recurrent Tumor Visible
n=3 Participants
All participants with recurrent tumor visible assessed for MTD.
Level 1 Cohort 1, Level 2 Cohort 1, and Level 3 Cohort 1:
Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
All Participants With Recurrent Tumor NOT Visible
n=3 Participants
All participants with recurrent tumor NOT visible assessed for MTD.
Level 1 Cohort 2, Level 2 Cohort 2, and Level 3 Cohort 2:
Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
LEVEL 3/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 10 Fractions
n=9 Participants
LEVEL 3/COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
LEVEL 1/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 20 Fractions
n=3 Participants
LEVEL 1/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 20 fractions: Dose to prostate bed 56.4 Gray (Gy) in 2.82 Gy fractions.
|
LEVEL 2/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 15 Fractions
n=3 Participants
LEVEL 2/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 15 fractions: Dose to prostate bed 51.2 Gray (Gy) in 3.41 Gy fractions.
|
LEVEL 3/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 10 Fractions
n=9 Participants
LEVEL 3/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
|---|---|---|---|---|---|---|
|
Number of Participants With a Dose-limiting Toxicity (DLT)
|
0 Participants
|
0 Participants
|
0 Participants
|
0 Participants
|
0 Participants
|
0 Participants
|
Adverse Events
LEVEL 1/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 20 Fractions
LEVEL 2/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 15 Fractions
LEVEL 3/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 10 Fractions
LEVEL 1/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 20 Fractions
LEVEL 2/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 15 Fractions
LEVEL 3/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 10 Fractions
Serious adverse events
| Measure |
LEVEL 1/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 20 Fractions
n=3 participants at risk
LEVEL 1/COHORT 1: Recurrent tumor visible; prostate bed with integrated boost. 20 fractions: Dose to prostate bed 45.8 Gray (Gy) in 2.29 Gy fractions; Dose to tumor 60.4 Gy in 3.02 Gy fractions.
|
LEVEL 2/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 15 Fractions
n=3 participants at risk
LEVEL 2/COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 15 fractions: Dose to prostate bed 41.85 Gray (Gy) in 2.79 Gy fractions; Dose to tumor 54.6 Gy in 3.64 Gy fractions.
|
LEVEL 3/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 10 Fractions
n=9 participants at risk
LEVEL 3/COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
LEVEL 1/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 20 Fractions
n=3 participants at risk
LEVEL 1/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 20 fractions: Dose to prostate bed 56.4 Gray (Gy) in 2.82 Gy fractions.
|
LEVEL 2/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 15 Fractions
n=3 participants at risk
LEVEL 2/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 15 fractions: Dose to prostate bed 51.2 Gray (Gy) in 3.41 Gy fractions.
|
LEVEL 3/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 10 Fractions
n=9 participants at risk
LEVEL 3/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
|---|---|---|---|---|---|---|
|
Musculoskeletal and connective tissue disorders
Back pain
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
Other adverse events
| Measure |
LEVEL 1/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 20 Fractions
n=3 participants at risk
LEVEL 1/COHORT 1: Recurrent tumor visible; prostate bed with integrated boost. 20 fractions: Dose to prostate bed 45.8 Gray (Gy) in 2.29 Gy fractions; Dose to tumor 60.4 Gy in 3.02 Gy fractions.
|
LEVEL 2/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 15 Fractions
n=3 participants at risk
LEVEL 2/COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 15 fractions: Dose to prostate bed 41.85 Gray (Gy) in 2.79 Gy fractions; Dose to tumor 54.6 Gy in 3.64 Gy fractions.
|
LEVEL 3/COHORT 1: Recurrent Tumor Visible; Prostate Bed With Integrated Boost - 10 Fractions
n=9 participants at risk
LEVEL 3/COHORT 1: Recurrent tumor visible, prostate bed with integrated boost. 10 fractions: Dose to prostate bed 36.4 Gray (Gy) in 3.64 Gy fractions; Dose to tumor 47.1 Gy in 4.71 Gy fractions.
|
LEVEL 1/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 20 Fractions
n=3 participants at risk
LEVEL 1/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 20 fractions: Dose to prostate bed 56.4 Gray (Gy) in 2.82 Gy fractions.
|
LEVEL 2/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 15 Fractions
n=3 participants at risk
LEVEL 2/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 15 fractions: Dose to prostate bed 51.2 Gray (Gy) in 3.41 Gy fractions.
|
LEVEL 3/COHORT 2: Recurrent Tumor NOT Visible; Prostate Bed Irradiation Only - 10 Fractions
n=9 participants at risk
LEVEL 3/COHORT 2: Recurrent tumor NOT visible, prostate bed irradiation only. 10 fractions: Dose to prostate bed 44.2 Gray (Gy) in 4.42 Gy fractions.
|
|---|---|---|---|---|---|---|
|
Psychiatric disorders
Anxiety
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
General disorders
Fatigue
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
66.7%
2/3 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
22.2%
2/9 • Number of events 5 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Vascular disorders
Hypertension
|
33.3%
1/3 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 5 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Musculoskeletal and connective tissue disorders
Arthralgia
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Investigations
Aspartate aminotransferase increased
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
General disorders
Edema limbs
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Gastrointestinal disorders
Abdominal pain
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Skin and subcutaneous tissue disorders
Alopecia
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Gastrointestinal disorders
Anal hemorrhage
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Gastrointestinal disorders
Anal pain
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Blood and lymphatic system disorders
Anemia
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Musculoskeletal and connective tissue disorders
Back pain
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Infections and infestations
Bronchial infection
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Cardiac disorders
Cardiac disorders - Other, palpitations, PVC?s, dizziness, history of chest pain
|
33.3%
1/3 • Number of events 3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
General disorders
Chills
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Hepatobiliary disorders
Cholecystitis
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Gastrointestinal disorders
Constipation
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
22.2%
2/9 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Reproductive system and breast disorders
Cystitis noninfective
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 3 • Date treatment consent signed to date off study, an average of 25 months.
|
22.2%
2/9 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Psychiatric disorders
Depression
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Gastrointestinal disorders
Diarrhea
|
66.7%
2/3 • Number of events 3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
22.2%
2/9 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
55.6%
5/9 • Number of events 5 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Nervous system disorders
Dizziness
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Gastrointestinal disorders
Fecal incontinence
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
22.2%
2/9 • Number of events 3 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Musculoskeletal and connective tissue disorders
Flank pain
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Gastrointestinal disorders
Flatulence
|
33.3%
1/3 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
66.7%
2/3 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
3/9 • Number of events 7 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
3/9 • Number of events 4 • Date treatment consent signed to date off study, an average of 25 months.
|
|
General disorders
Flu like symptoms
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Hepatobiliary disorders
Gallbladder obstruction
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Gastrointestinal disorders
Gastritis
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Gastrointestinal disorders
Gastroesophageal reflux disease
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Gastrointestinal disorders
Gastrointestinal disorders - Other, fecal urgency
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Gastrointestinal disorders
Gastrointestinal disorders - Other, hernia
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Gastrointestinal disorders
Gastrointestinal disorders - Other, passing stool with gas
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Reproductive system and breast disorders
Genital edema
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Nervous system disorders
Headache
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Renal and urinary disorders
Hematuria
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Gastrointestinal disorders
Hemorrhoidal hemorrhage
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
3/9 • Number of events 3 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Gastrointestinal disorders
Hemorrhoids
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
77.8%
7/9 • Number of events 9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Vascular disorders
Hot flashes
|
66.7%
2/3 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
66.7%
2/3 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Injury, poisoning and procedural complications
Injury, poisoning and procedural complications - Other, Right great toe "Turf toe"
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Injury, poisoning and procedural complications
Injury, poisoning and procedural complications - Other, Right left second toe injury
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Reproductive system and breast disorders
Libido decreased
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Infections and infestations
Lung infection
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Musculoskeletal and connective tissue disorders
Non-cardiac chest pain
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
General disorders
Pain
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Musculoskeletal and connective tissue disorders
Pain in extremity
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
22.2%
2/9 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Gastrointestinal disorders
Proctitis
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
66.7%
2/3 • Number of events 4 • Date treatment consent signed to date off study, an average of 25 months.
|
66.7%
6/9 • Number of events 7 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
66.7%
2/3 • Number of events 3 • Date treatment consent signed to date off study, an average of 25 months.
|
100.0%
9/9 • Number of events 17 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Skin and subcutaneous tissue disorders
Pruritus
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Psychiatric disorders
Psychiatric disorders - Other, Post Traumatic Stress Disorder
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Gastrointestinal disorders
Rectal hemorrhage
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
22.2%
2/9 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Renal and urinary disorders
Renal and urinary disorders - Other, Nocturia
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Renal and urinary disorders
Renal and urinary disorders - Other, weak stream
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Reproductive system and breast disorders
Reproductive system and breast disorders - Other, Climacturia
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Reproductive system and breast disorders
Reproductive system and breast disorders - Other, Internal pulling sensation suprapubic
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Nervous system disorders
Transient ischemic attacks
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Infections and infestations
Sinusitis
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
22.2%
2/9 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Skin and subcutaneous tissue disorders
Skin and subcutaneous tissue disorders - Other, Gluteal cleft fissure
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Skin and subcutaneous tissue disorders
Skin and subcutaneous tissue disorders - Other, Hyperpigmented macule
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Skin and subcutaneous tissue disorders
Skin and subcutaneous tissue disorders - Other, Tinea cruris
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Skin and subcutaneous tissue disorders
Skin and subcutaneous tissue disorders - Other, contact dermatitis
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Infections and infestations
Skin infection
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Reproductive system and breast disorders
Testicular disorder
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Reproductive system and breast disorders
Testicular pain
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Infections and infestations
Tooth infection
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Infections and infestations
Upper respiratory infection
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Renal and urinary disorders
Urinary frequency
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
22.2%
2/9 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Renal and urinary disorders
Urinary incontinence
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
66.7%
2/3 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
3/9 • Number of events 4 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Infections and infestations
Urinary tract infection
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Renal and urinary disorders
Urinary tract obstruction
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Renal and urinary disorders
Urinary tract pain
|
100.0%
3/3 • Number of events 3 • Date treatment consent signed to date off study, an average of 25 months.
|
66.7%
2/3 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
3/9 • Number of events 3 • Date treatment consent signed to date off study, an average of 25 months.
|
100.0%
3/3 • Number of events 3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
3/9 • Number of events 4 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Renal and urinary disorders
Urinary urgency
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
22.2%
2/9 • Number of events 2 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
|
Injury, poisoning and procedural complications
Wrist fracture
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/9 • Date treatment consent signed to date off study, an average of 25 months.
|
0.00%
0/3 • Date treatment consent signed to date off study, an average of 25 months.
|
33.3%
1/3 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
11.1%
1/9 • Number of events 1 • Date treatment consent signed to date off study, an average of 25 months.
|
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place