Trial Outcomes & Findings for Umbralisib and Rituximab as Initial Therapy for Patients With Follicular Lymphoma and Marginal Zone Lymphoma (NCT NCT03919175)
NCT ID: NCT03919175
Last Updated: 2026-02-27
Results Overview
The frequency of patients who achieve a complete response per 2014 Lugano criteria.
Recruitment status
TERMINATED
Study phase
PHASE2
Target enrollment
18 participants
Primary outcome timeframe
2 years
Results posted on
2026-02-27
Participant Flow
Participant milestones
| Measure |
Umbralisib+Rituximab
* A treatment cycle is defined as 28 consecutive days.
* Umbralisib will be administered at 800 mg by mouth once daily on days 1-28 of cycles 1-24.
* Rituximab will be administered at 375 mg/m2 by intravenous infusion on Cycle 1 Day 1 and may be administered at 375 mg/m2 by intravenous infusion or at 1400 mg by subcutaneous injection on days 8, 15, 22 of cycle 1, day 1 of cycles 2 to 6, then every 8 weeks starting on day 1 of cycle 7 until completion of 24 cycles of umbralisib (i.e. every other cycle for 18 cycles or 9 doses, for a total of 15 doses of rituximab), or until progression or intolerance.
Umbralisib: Umbralisib is an investigational drug which blocks a protein called PI3K. PI3K is a protein that plays a role in the way cells grow. In this type of cancer, PI3K is increased and more active than usual. This helps the cancer cells to grow and survive.
Rituximab: Rituximab works by targeting the CD20 antigen on normal and malignant B-cells. Then the body's natural immune defenses are recruited to attack and kill the marked B-cells
|
|---|---|
|
Overall Study
STARTED
|
18
|
|
Overall Study
COMPLETED
|
18
|
|
Overall Study
NOT COMPLETED
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Number analyzed is 18 (inaccurate warning)
Baseline characteristics by cohort
| Measure |
Umbralisib+Rituximab
n=18 Participants
* A treatment cycle is defined as 28 consecutive days.
* Umbralisib will be administered at 800 mg by mouth once daily on days 1-28 of cycles 1-24.
* Rituximab will be administered at 375 mg/m2 by intravenous infusion on Cycle 1 Day 1 and may be administered at 375 mg/m2 by intravenous infusion or at 1400 mg by subcutaneous injection on days 8, 15, 22 of cycle 1, day 1 of cycles 2 to 6, then every 8 weeks starting on day 1 of cycle 7 until completion of 24 cycles of umbralisib (i.e. every other cycle for 18 cycles or 9 doses, for a total of 15 doses of rituximab), or until progression or intolerance.
Umbralisib: Umbralisib is an investigational drug which blocks a protein called PI3K. PI3K is a protein that plays a role in the way cells grow. In this type of cancer, PI3K is increased and more active than usual. This helps the cancer cells to grow and survive.
Rituximab: Rituximab works by targeting the CD20 antigen on normal and malignant B-cells. Then the body's natural immune defenses are recruited to attack and kill the marked B-cells
|
|---|---|
|
Age, Customized
Age 18 to <65
|
11 Participants
n=24 Participants • Number analyzed is 18 (inaccurate warning)
|
|
Age, Customized
Age 65 and older
|
7 Participants
n=24 Participants • Number analyzed is 18 (inaccurate warning)
|
|
Sex: Female, Male
Female
|
9 Participants
n=24 Participants
|
|
Sex: Female, Male
Male
|
9 Participants
n=24 Participants
|
|
Ethnicity (NIH/OMB)
Hispanic or Latino
|
0 Participants
n=24 Participants
|
|
Ethnicity (NIH/OMB)
Not Hispanic or Latino
|
0 Participants
n=24 Participants
|
|
Ethnicity (NIH/OMB)
Unknown or Not Reported
|
18 Participants
n=24 Participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
0 Participants
n=24 Participants
|
|
Race (NIH/OMB)
Asian
|
0 Participants
n=24 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=24 Participants
|
|
Race (NIH/OMB)
Black or African American
|
0 Participants
n=24 Participants
|
|
Race (NIH/OMB)
White
|
17 Participants
n=24 Participants
|
|
Race (NIH/OMB)
More than one race
|
0 Participants
n=24 Participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
1 Participants
n=24 Participants
|
PRIMARY outcome
Timeframe: 2 yearsThe frequency of patients who achieve a complete response per 2014 Lugano criteria.
Outcome measures
| Measure |
Umbralisib+Rituximab
n=18 Participants
* A treatment cycle is defined as 28 consecutive days.
* Umbralisib will be administered at 800 mg by mouth once daily on days 1-28 of cycles 1-24.
* Rituximab will be administered at 375 mg/m2 by intravenous infusion on Cycle 1 Day 1 and may be administered at 375 mg/m2 by intravenous infusion or at 1400 mg by subcutaneous injection on days 8, 15, 22 of cycle 1, day 1 of cycles 2 to 6, then every 8 weeks starting on day 1 of cycle 7 until completion of 24 cycles of umbralisib (i.e. every other cycle for 18 cycles or 9 doses, for a total of 15 doses of rituximab), or until progression or intolerance.
Umbralisib: Umbralisib is an investigational drug which blocks a protein called PI3K. PI3K is a protein that plays a role in the way cells grow. In this type of cancer, PI3K is increased and more active than usual. This helps the cancer cells to grow and survive.
Rituximab: Rituximab works by targeting the CD20 antigen on normal and malignant B-cells. Then the body's natural immune defenses are recruited to attack and kill the marked B-cells
|
|---|---|
|
Complete Response Rate
|
7 Participants
|
SECONDARY outcome
Timeframe: 2 yearsThe frequency of patients who achieve a complete or partial response per 2014 Lugano criteria
Outcome measures
| Measure |
Umbralisib+Rituximab
n=18 Participants
* A treatment cycle is defined as 28 consecutive days.
* Umbralisib will be administered at 800 mg by mouth once daily on days 1-28 of cycles 1-24.
* Rituximab will be administered at 375 mg/m2 by intravenous infusion on Cycle 1 Day 1 and may be administered at 375 mg/m2 by intravenous infusion or at 1400 mg by subcutaneous injection on days 8, 15, 22 of cycle 1, day 1 of cycles 2 to 6, then every 8 weeks starting on day 1 of cycle 7 until completion of 24 cycles of umbralisib (i.e. every other cycle for 18 cycles or 9 doses, for a total of 15 doses of rituximab), or until progression or intolerance.
Umbralisib: Umbralisib is an investigational drug which blocks a protein called PI3K. PI3K is a protein that plays a role in the way cells grow. In this type of cancer, PI3K is increased and more active than usual. This helps the cancer cells to grow and survive.
Rituximab: Rituximab works by targeting the CD20 antigen on normal and malignant B-cells. Then the body's natural immune defenses are recruited to attack and kill the marked B-cells
|
|---|---|
|
Overall Response Rate
Complete response
|
7 Participants
|
|
Overall Response Rate
Partial response
|
7 Participants
|
|
Overall Response Rate
Stable disease
|
4 Participants
|
|
Overall Response Rate
Progressive disease
|
0 Participants
|
SECONDARY outcome
Timeframe: 2 yearsThe median progression-free survival using Kaplan-Meier method with time of registration as time origin.
Outcome measures
| Measure |
Umbralisib+Rituximab
n=18 Participants
* A treatment cycle is defined as 28 consecutive days.
* Umbralisib will be administered at 800 mg by mouth once daily on days 1-28 of cycles 1-24.
* Rituximab will be administered at 375 mg/m2 by intravenous infusion on Cycle 1 Day 1 and may be administered at 375 mg/m2 by intravenous infusion or at 1400 mg by subcutaneous injection on days 8, 15, 22 of cycle 1, day 1 of cycles 2 to 6, then every 8 weeks starting on day 1 of cycle 7 until completion of 24 cycles of umbralisib (i.e. every other cycle for 18 cycles or 9 doses, for a total of 15 doses of rituximab), or until progression or intolerance.
Umbralisib: Umbralisib is an investigational drug which blocks a protein called PI3K. PI3K is a protein that plays a role in the way cells grow. In this type of cancer, PI3K is increased and more active than usual. This helps the cancer cells to grow and survive.
Rituximab: Rituximab works by targeting the CD20 antigen on normal and malignant B-cells. Then the body's natural immune defenses are recruited to attack and kill the marked B-cells
|
|---|---|
|
Progression Free Survival
|
NA years
The median PFS and associated confidence intervals were not reached for this study. This is due to an insufficient number of participants with events.
|
SECONDARY outcome
Timeframe: 2 YearsThe median overall survival using Kaplan-Meier method with time of registration as time origin.
Outcome measures
| Measure |
Umbralisib+Rituximab
n=18 Participants
* A treatment cycle is defined as 28 consecutive days.
* Umbralisib will be administered at 800 mg by mouth once daily on days 1-28 of cycles 1-24.
* Rituximab will be administered at 375 mg/m2 by intravenous infusion on Cycle 1 Day 1 and may be administered at 375 mg/m2 by intravenous infusion or at 1400 mg by subcutaneous injection on days 8, 15, 22 of cycle 1, day 1 of cycles 2 to 6, then every 8 weeks starting on day 1 of cycle 7 until completion of 24 cycles of umbralisib (i.e. every other cycle for 18 cycles or 9 doses, for a total of 15 doses of rituximab), or until progression or intolerance.
Umbralisib: Umbralisib is an investigational drug which blocks a protein called PI3K. PI3K is a protein that plays a role in the way cells grow. In this type of cancer, PI3K is increased and more active than usual. This helps the cancer cells to grow and survive.
Rituximab: Rituximab works by targeting the CD20 antigen on normal and malignant B-cells. Then the body's natural immune defenses are recruited to attack and kill the marked B-cells
|
|---|---|
|
Overall Survival
|
NA years
The median OS and associated confidence intervals were not reached for this study. This is due to an insufficient number of participants with events.
|
SECONDARY outcome
Timeframe: 2 yearsOutcome measures
| Measure |
Umbralisib+Rituximab
n=18 Participants
* A treatment cycle is defined as 28 consecutive days.
* Umbralisib will be administered at 800 mg by mouth once daily on days 1-28 of cycles 1-24.
* Rituximab will be administered at 375 mg/m2 by intravenous infusion on Cycle 1 Day 1 and may be administered at 375 mg/m2 by intravenous infusion or at 1400 mg by subcutaneous injection on days 8, 15, 22 of cycle 1, day 1 of cycles 2 to 6, then every 8 weeks starting on day 1 of cycle 7 until completion of 24 cycles of umbralisib (i.e. every other cycle for 18 cycles or 9 doses, for a total of 15 doses of rituximab), or until progression or intolerance.
Umbralisib: Umbralisib is an investigational drug which blocks a protein called PI3K. PI3K is a protein that plays a role in the way cells grow. In this type of cancer, PI3K is increased and more active than usual. This helps the cancer cells to grow and survive.
Rituximab: Rituximab works by targeting the CD20 antigen on normal and malignant B-cells. Then the body's natural immune defenses are recruited to attack and kill the marked B-cells
|
|---|---|
|
Number of Participants With Adverse Events
|
15 Participants
|
Adverse Events
Umbralisib+Rituximab
Serious events: 9 serious events
Other events: 15 other events
Deaths: 2 deaths
Serious adverse events
| Measure |
Umbralisib+Rituximab
n=18 participants at risk
* A treatment cycle is defined as 28 consecutive days.
* Umbralisib will be administered at 800 mg by mouth once daily on days 1-28 of cycles 1-24.
* Rituximab will be administered at 375 mg/m2 by intravenous infusion on Cycle 1 Day 1 and may be administered at 375 mg/m2 by intravenous infusion or at 1400 mg by subcutaneous injection on days 8, 15, 22 of cycle 1, day 1 of cycles 2 to 6, then every 8 weeks starting on day 1 of cycle 7 until completion of 24 cycles of umbralisib (i.e. every other cycle for 18 cycles or 9 doses, for a total of 15 doses of rituximab), or until progression or intolerance.
Umbralisib: Umbralisib is an investigational drug which blocks a protein called PI3K. PI3K is a protein that plays a role in the way cells grow. In this type of cancer, PI3K is increased and more active than usual. This helps the cancer cells to grow and survive.
Rituximab: Rituximab works by targeting the CD20 antigen on normal and malignant B-cells. Then the body's natural immune defenses are recruited to attack and kill the marked B-cells
|
|---|---|
|
Gastrointestinal disorders
Cholecystitis
|
5.6%
1/18 • Approximately 24 months
|
|
Immune system disorders
Allergic reaction
|
5.6%
1/18 • Approximately 24 months
|
|
Respiratory, thoracic and mediastinal disorders
Pneumonitis
|
5.6%
1/18 • Approximately 24 months
|
|
Infections and infestations
Infections and infestations - Other, specify
|
5.6%
1/18 • Approximately 24 months
|
|
Skin and subcutaneous tissue disorders
Rash maculo-papular
|
11.1%
2/18 • Approximately 24 months
|
|
General disorders
General disorders and administration site conditions - Other, specify
|
5.6%
1/18 • Approximately 24 months
|
|
General disorders
Back pain
|
5.6%
1/18 • Approximately 24 months
|
|
General disorders
Pain
|
5.6%
1/18 • Approximately 24 months
|
Other adverse events
| Measure |
Umbralisib+Rituximab
n=18 participants at risk
* A treatment cycle is defined as 28 consecutive days.
* Umbralisib will be administered at 800 mg by mouth once daily on days 1-28 of cycles 1-24.
* Rituximab will be administered at 375 mg/m2 by intravenous infusion on Cycle 1 Day 1 and may be administered at 375 mg/m2 by intravenous infusion or at 1400 mg by subcutaneous injection on days 8, 15, 22 of cycle 1, day 1 of cycles 2 to 6, then every 8 weeks starting on day 1 of cycle 7 until completion of 24 cycles of umbralisib (i.e. every other cycle for 18 cycles or 9 doses, for a total of 15 doses of rituximab), or until progression or intolerance.
Umbralisib: Umbralisib is an investigational drug which blocks a protein called PI3K. PI3K is a protein that plays a role in the way cells grow. In this type of cancer, PI3K is increased and more active than usual. This helps the cancer cells to grow and survive.
Rituximab: Rituximab works by targeting the CD20 antigen on normal and malignant B-cells. Then the body's natural immune defenses are recruited to attack and kill the marked B-cells
|
|---|---|
|
Infections and infestations
Conjunctivitis
|
16.7%
3/18 • Approximately 24 months
|
|
Respiratory, thoracic and mediastinal disorders
Cough
|
16.7%
3/18 • Approximately 24 months
|
|
Nervous system disorders
Dizziness
|
16.7%
3/18 • Approximately 24 months
|
|
General disorders
Fever
|
16.7%
3/18 • Approximately 24 months
|
|
Gastrointestinal disorders
Gastroesophageal reflux disease
|
16.7%
3/18 • Approximately 24 months
|
|
Nervous system disorders
Nervous system disorders - Other, specify
|
16.7%
3/18 • Approximately 24 months
|
|
Investigations
Neutrophil count decreased
|
16.7%
3/18 • Approximately 24 months
|
|
Investigations
Platelet count decreased
|
16.7%
3/18 • Approximately 24 months
|
|
Gastrointestinal disorders
Colitis
|
27.8%
5/18 • Approximately 24 months
|
|
Psychiatric disorders
Depression
|
11.1%
2/18 • Approximately 24 months
|
|
Nervous system disorders
Dysgeusia
|
11.1%
2/18 • Approximately 24 months
|
|
Infections and infestations
Folliculitis
|
11.1%
2/18 • Approximately 24 months
|
|
Vascular disorders
Hot flashes
|
11.1%
2/18 • Approximately 24 months
|
|
General disorders
Non-cardiac chest pain
|
11.1%
2/18 • Approximately 24 months
|
|
Skin and subcutaneous tissue disorders
Rash acneiform
|
11.1%
2/18 • Approximately 24 months
|
|
Respiratory, thoracic and mediastinal disorders
Respiratory, thoracic and mediastinal disorders - Other, specify
|
11.1%
2/18 • Approximately 24 months
|
|
Nervous system disorders
Tremor
|
11.1%
2/18 • Approximately 24 months
|
|
Gastrointestinal disorders
Vomiting
|
11.1%
2/18 • Approximately 24 months
|
|
Gastrointestinal disorders
Abdominal distension
|
5.6%
1/18 • Approximately 24 months
|
|
Skin and subcutaneous tissue disorders
Alopecia
|
5.6%
1/18 • Approximately 24 months
|
|
Respiratory, thoracic and mediastinal disorders
Apnea
|
5.6%
1/18 • Approximately 24 months
|
|
Musculoskeletal and connective tissue disorders
Arthralgia
|
5.6%
1/18 • Approximately 24 months
|
|
Musculoskeletal and connective tissue disorders
Arthritis
|
5.6%
1/18 • Approximately 24 months
|
|
Infections and infestations
Bacteremia
|
5.6%
1/18 • Approximately 24 months
|
|
Gastrointestinal disorders
Bloating
|
5.6%
1/18 • Approximately 24 months
|
|
Blood and lymphatic system disorders
Blood and lymphatic system disorders - Other, specify
|
5.6%
1/18 • Approximately 24 months
|
|
Investigations
Blood lactate dehydrogenase increased
|
5.6%
1/18 • Approximately 24 months
|
|
Eye disorders
Blurred vision
|
5.6%
1/18 • Approximately 24 months
|
|
Musculoskeletal and connective tissue disorders
Bone pain
|
5.6%
1/18 • Approximately 24 months
|
|
Injury, poisoning and procedural complications
Bruising
|
5.6%
1/18 • Approximately 24 months
|
|
Musculoskeletal and connective tissue disorders
Buttock pain
|
5.6%
1/18 • Approximately 24 months
|
|
Hepatobiliary disorders
Cholecystitis
|
5.6%
1/18 • Approximately 24 months
|
|
Eye disorders
Dry eye
|
5.6%
1/18 • Approximately 24 months
|
|
Gastrointestinal disorders
Dry mouth
|
5.6%
1/18 • Approximately 24 months
|
|
Ear and labyrinth disorders
Ear pain
|
5.6%
1/18 • Approximately 24 months
|
|
General disorders
Edema face
|
5.6%
1/18 • Approximately 24 months
|
|
Injury, poisoning and procedural complications
Fall
|
5.6%
1/18 • Approximately 24 months
|
|
Gastrointestinal disorders
Fecal incontinence
|
5.6%
1/18 • Approximately 24 months
|
|
Musculoskeletal and connective tissue disorders
Flank pain
|
5.6%
1/18 • Approximately 24 months
|
|
Injury, poisoning and procedural complications
Fracture
|
5.6%
1/18 • Approximately 24 months
|
|
General disorders
Gait disturbance
|
5.6%
1/18 • Approximately 24 months
|
|
Gastrointestinal disorders
Gastritis
|
5.6%
1/18 • Approximately 24 months
|
|
Vascular disorders
Hematoma
|
5.6%
1/18 • Approximately 24 months
|
|
Gastrointestinal disorders
Hemorrhoids
|
5.6%
1/18 • Approximately 24 months
|
|
Hepatobiliary disorders
Hepatobiliary disorders - Other, specify
|
5.6%
1/18 • Approximately 24 months
|
|
Metabolism and nutrition disorders
Hyperglycemia
|
5.6%
1/18 • Approximately 24 months
|
|
Metabolism and nutrition disorders
Hyperlipidemia
|
5.6%
1/18 • Approximately 24 months
|
|
Metabolism and nutrition disorders
Hypophosphatemia
|
5.6%
1/18 • Approximately 24 months
|
|
Respiratory, thoracic and mediastinal disorders
Hypoxia
|
5.6%
1/18 • Approximately 24 months
|
|
Gastrointestinal disorders
Ileus
|
5.6%
1/18 • Approximately 24 months
|
|
Immune system disorders
Immune system disorders - Other, specify
|
5.6%
1/18 • Approximately 24 months
|
|
Infections and infestations
Infections and infestations - Other, specify
|
5.6%
1/18 • Approximately 24 months
|
|
Investigations
Investigations - Other, specify
|
5.6%
1/18 • Approximately 24 months
|
|
Blood and lymphatic system disorders
Leukocytosis
|
5.6%
1/18 • Approximately 24 months
|
|
Blood and lymphatic system disorders
Lymph node pain
|
5.6%
1/18 • Approximately 24 months
|
|
Investigations
Lymphocyte count decreased
|
5.6%
1/18 • Approximately 24 months
|
|
Investigations
Lymphocyte count increased
|
5.6%
1/18 • Approximately 24 months
|
|
General disorders
Malaise
|
5.6%
1/18 • Approximately 24 months
|
|
Metabolism and nutrition disorders
Metabolism and nutrition disorders - Other, specify
|
5.6%
1/18 • Approximately 24 months
|
|
Gastrointestinal disorders
Mucositis oral
|
5.6%
1/18 • Approximately 24 months
|
|
Musculoskeletal and connective tissue disorders
Muscle cramp
|
5.6%
1/18 • Approximately 24 months
|
|
Musculoskeletal and connective tissue disorders
Musculoskeletal and connective tissue disorder - Other, specify
|
5.6%
1/18 • Approximately 24 months
|
|
Metabolism and nutrition disorders
Obesity
|
5.6%
1/18 • Approximately 24 months
|
|
Gastrointestinal disorders
Oral pain
|
5.6%
1/18 • Approximately 24 months
|
|
Infections and infestations
Otitis media
|
5.6%
1/18 • Approximately 24 months
|
|
Nervous system disorders
Paresthesia
|
5.6%
1/18 • Approximately 24 months
|
|
Skin and subcutaneous tissue disorders
Pruritus
|
5.6%
1/18 • Approximately 24 months
|
|
Psychiatric disorders
Psychiatric disorders - Other, specify
|
5.6%
1/18 • Approximately 24 months
|
|
Respiratory, thoracic and mediastinal disorders
Pulmonary hypertension
|
5.6%
1/18 • Approximately 24 months
|
|
Respiratory, thoracic and mediastinal disorders
Rhinorrhea
|
5.6%
1/18 • Approximately 24 months
|
|
Respiratory, thoracic and mediastinal disorders
Sinus pain
|
5.6%
1/18 • Approximately 24 months
|
|
Skin and subcutaneous tissue disorders
Skin ulceration
|
5.6%
1/18 • Approximately 24 months
|
|
Ear and labyrinth disorders
Tinnitus
|
5.6%
1/18 • Approximately 24 months
|
|
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
Tumor pain
|
5.6%
1/18 • Approximately 24 months
|
|
Renal and urinary disorders
Urinary frequency
|
5.6%
1/18 • Approximately 24 months
|
|
Infections and infestations
Vaginal infection
|
5.6%
1/18 • Approximately 24 months
|
|
Reproductive system and breast disorders
Vaginal inflammation
|
5.6%
1/18 • Approximately 24 months
|
|
Respiratory, thoracic and mediastinal disorders
Voice alteration
|
5.6%
1/18 • Approximately 24 months
|
|
Investigations
Weight gain
|
5.6%
1/18 • Approximately 24 months
|
|
Investigations
Weight loss
|
5.6%
1/18 • Approximately 24 months
|
|
General disorders
Fatigue
|
83.3%
15/18 • Approximately 24 months
|
|
Gastrointestinal disorders
Diarrhea
|
77.8%
14/18 • Approximately 24 months
|
|
Gastrointestinal disorders
Nausea
|
61.1%
11/18 • Approximately 24 months
|
|
Investigations
Aspartate aminotransferase increased
|
44.4%
8/18 • Approximately 24 months
|
|
Gastrointestinal disorders
Abdominal pain
|
38.9%
7/18 • Approximately 24 months
|
|
Investigations
Alanine aminotransferase increased
|
38.9%
7/18 • Approximately 24 months
|
|
Psychiatric disorders
Anxiety
|
38.9%
7/18 • Approximately 24 months
|
|
Psychiatric disorders
Insomnia
|
38.9%
7/18 • Approximately 24 months
|
|
Skin and subcutaneous tissue disorders
Rash maculo-papular
|
33.3%
6/18 • Approximately 24 months
|
|
Metabolism and nutrition disorders
Anorexia
|
27.8%
5/18 • Approximately 24 months
|
|
Musculoskeletal and connective tissue disorders
Back pain
|
27.8%
5/18 • Approximately 24 months
|
|
Vascular disorders
Hypertension
|
27.8%
5/18 • Approximately 24 months
|
|
Injury, poisoning and procedural complications
Infusion related reaction
|
27.8%
5/18 • Approximately 24 months
|
|
General disorders
Injection site reaction
|
27.8%
5/18 • Approximately 24 months
|
|
Musculoskeletal and connective tissue disorders
Pain in extremity
|
27.8%
5/18 • Approximately 24 months
|
|
Infections and infestations
Upper respiratory infection
|
27.8%
5/18 • Approximately 24 months
|
|
Blood and lymphatic system disorders
Anemia
|
22.2%
4/18 • Approximately 24 months
|
|
Respiratory, thoracic and mediastinal disorders
Dyspnea
|
22.2%
4/18 • Approximately 24 months
|
|
General disorders
General disorders and administration site conditions - Other, specify
|
22.2%
4/18 • Approximately 24 months
|
|
Nervous system disorders
Headache
|
22.2%
4/18 • Approximately 24 months
|
|
General disorders
Pain
|
22.2%
4/18 • Approximately 24 months
|
|
Skin and subcutaneous tissue disorders
Skin and subcutaneous tissue disorders - Other, specify
|
22.2%
4/18 • Approximately 24 months
|
|
Respiratory, thoracic and mediastinal disorders
Sore throat
|
22.2%
4/18 • Approximately 24 months
|
|
Investigations
Alkaline phosphatase increased
|
16.7%
3/18 • Approximately 24 months
|
|
General disorders
Chills
|
16.7%
3/18 • Approximately 24 months
|
Additional Information
Jacob D. Soumerai, MD; Associate Professor of Medicine
Massachusetts General Hospital
Phone: 617-792-0547
Email: [email protected]
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place