Trial Outcomes & Findings for Oral Paricalcitol in Kidney Transplant Recipients (NCT NCT00587158)

NCT ID: NCT00587158

Last Updated: 2013-05-13

Results Overview

Parathyroid hormone (PTH) is a measure of how well the parathyroid gland is working and is measured by a blood test. Hyperparathyroidism (increased PTH) is defined as PTH blood value greater than 65 picograms/milliliter in the absence of hypocalcemia (low calcium) or if the subject had a parathyroidectomy (surgical removal of parathyroid glands) during the first year post-transplant.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

100 participants

Primary outcome timeframe

1 year post kidney transplant

Results posted on

2013-05-13

Participant Flow

Patients to undergo kidney transplantation at Mayo Clinic facilities in Rochester, Minnesota and in Scottsdale, Arizona and scheduled to receive corticosteroid avoidance anti-rejection therapy were screened for enrollment into the study.

112 patients were approached for enrollment. Of those, 4 patient's treating physicians did not think corticosteroid free immunosuppression was appropriate, 3 had their transplants cancelled, 3 were found to be vitamin D deficient, 1 withdrew consent prior to randomization \& 1 had a positive final crossmatch and hence were excluded from the study.

Participant milestones

Participant milestones
Measure
Immunosuppression Without Paricalcitol (Control)
Subjects will receive the standard immunosuppressive therapies consisting of induction therapy with Alemtuzumab (Campath®) and Methylprednisolone (Solumedrol®), then maintained with corticosteroid avoidance using Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
Subjects will receive the standard immunosuppressive therapy consisting of induction therapy with Alemtuzumab (Campath®) and Methylprednisolone (Solumedrol®), then maintained with corticosteroid avoidance using Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®). In addition, subjects in this group will receive the study medication paricalcitol (Zemplar®).
Overall Study
STARTED
49
51
Overall Study
Continued in Study
45
46
Overall Study
COMPLETED
44
43
Overall Study
NOT COMPLETED
5
8

Reasons for withdrawal

Reasons for withdrawal
Measure
Immunosuppression Without Paricalcitol (Control)
Subjects will receive the standard immunosuppressive therapies consisting of induction therapy with Alemtuzumab (Campath®) and Methylprednisolone (Solumedrol®), then maintained with corticosteroid avoidance using Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
Subjects will receive the standard immunosuppressive therapy consisting of induction therapy with Alemtuzumab (Campath®) and Methylprednisolone (Solumedrol®), then maintained with corticosteroid avoidance using Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®). In addition, subjects in this group will receive the study medication paricalcitol (Zemplar®).
Overall Study
Did not want to do 24 hr urine collect.
4
3
Overall Study
Physician Decision
0
1
Overall Study
Lost to Follow-up
1
2
Overall Study
Death
0
1
Overall Study
Subject did not want to take study med
0
1

Baseline Characteristics

Oral Paricalcitol in Kidney Transplant Recipients

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Immunosuppression Without Paricalcitol (Control)
n=49 Participants
Subjects will receive the standard immunosuppressive therapies of Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®), Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
n=51 Participants
Subjects will receive the standard immunosuppressive medications; Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®),Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®), and in addition will receive the study medication paricalcitol (Zemplar®).
Total
n=100 Participants
Total of all reporting groups
Age Continuous
47.7 years
STANDARD_DEVIATION 10.0 • n=99 Participants
48.5 years
STANDARD_DEVIATION 10.3 • n=107 Participants
48.1 years
STANDARD_DEVIATION 10.1 • n=206 Participants
Sex: Female, Male
Female
16 Participants
n=99 Participants
18 Participants
n=107 Participants
34 Participants
n=206 Participants
Sex: Female, Male
Male
33 Participants
n=99 Participants
33 Participants
n=107 Participants
66 Participants
n=206 Participants
Race/Ethnicity, Customized
American Indian or Alaska Native
2 Participants
n=99 Participants
0 Participants
n=107 Participants
2 Participants
n=206 Participants
Race/Ethnicity, Customized
Asian
1 Participants
n=99 Participants
0 Participants
n=107 Participants
1 Participants
n=206 Participants
Race/Ethnicity, Customized
Native Hawaiian or Other Pacific Islander
0 Participants
n=99 Participants
1 Participants
n=107 Participants
1 Participants
n=206 Participants
Race/Ethnicity, Customized
Black or African American
3 Participants
n=99 Participants
0 Participants
n=107 Participants
3 Participants
n=206 Participants
Race/Ethnicity, Customized
White
42 Participants
n=99 Participants
49 Participants
n=107 Participants
91 Participants
n=206 Participants
Race/Ethnicity, Customized
More than one race
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
Race/Ethnicity, Customized
Unknown or Not Reported
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants
Race/Ethnicity, Customized
Hispanic
1 Participants
n=99 Participants
1 Participants
n=107 Participants
2 Participants
n=206 Participants
Region of Enrollment
United States
49 participants
n=99 Participants
51 participants
n=107 Participants
100 participants
n=206 Participants
Diabetes
12 participants
n=99 Participants
10 participants
n=107 Participants
22 participants
n=206 Participants
First transplant
47 participants
n=99 Participants
50 participants
n=107 Participants
97 participants
n=206 Participants
Cause of End-Stage Renal Disease
Adult Polycystic Kidney Disease
14 participants
n=99 Participants
16 participants
n=107 Participants
30 participants
n=206 Participants
Cause of End-Stage Renal Disease
Diabetic
10 participants
n=99 Participants
8 participants
n=107 Participants
18 participants
n=206 Participants
Cause of End-Stage Renal Disease
Glomerulonephritis
17 participants
n=99 Participants
16 participants
n=107 Participants
33 participants
n=206 Participants
Cause of End-Stage Renal Disease
Hypertension
1 participants
n=99 Participants
3 participants
n=107 Participants
4 participants
n=206 Participants
Cause of End-Stage Renal Disease
Other
7 participants
n=99 Participants
8 participants
n=107 Participants
15 participants
n=206 Participants
Living kidney donor
48 participants
n=99 Participants
48 participants
n=107 Participants
96 participants
n=206 Participants
Degree of interstitial fibrosis
Mild fibrosis at baseline
2 Participants
n=99 Participants
3 Participants
n=107 Participants
5 Participants
n=206 Participants
Degree of interstitial fibrosis
Moderate to severe fibrosis at baseline
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=206 Participants

PRIMARY outcome

Timeframe: 1 year post kidney transplant

Population: Analysis was performed by the intention-to-treat principle, comprised of all subjects enrolled, who will have taken at least one dose of study medication and have both screening and any post-screening efficacy data recorded. The last observation was carried forward for missing values.

Parathyroid hormone (PTH) is a measure of how well the parathyroid gland is working and is measured by a blood test. Hyperparathyroidism (increased PTH) is defined as PTH blood value greater than 65 picograms/milliliter in the absence of hypocalcemia (low calcium) or if the subject had a parathyroidectomy (surgical removal of parathyroid glands) during the first year post-transplant.

Outcome measures

Outcome measures
Measure
Immunosuppression Without Paricalcitol (Control)
n=49 Participants
Subjects will receive the standard immunosuppressive therapies of Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®), Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
n=51 Participants
Subjects will receive the standard immunosuppressive medications; Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®),Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®), and in addition will receive the study medication paricalcitol (Zemplar®).
Number of Subjects With Hyperparathyroidism at One Year
31 Participants
15 Participants

SECONDARY outcome

Timeframe: 1 year post kidney transplant

Population: Per-protocol analysis. Data were not available for 2 control subjects and 2 treatment subjects, as these subjects did not have the DEXA scan of the hip done at one year. \[Control n=42/ Treatment=41\]

Osteopenia/Osteoporosis are conditions where bone mineral density is lower than normal, reported by T-scores, measurements of the hip made using an Dual Energy X-ray Absorptiometry (DEXA) scan. The T-score is measured and compared to a normal healthy adult. A normal bone density results in a T-score between +1.0 and -1.0. A T-score of less than or equal to -1.5 was used for this study to define the presence of osteopenia/osteoporosis. Each participant will be categorized as having or not having osteopenia/osteoporosis of the hip at the end of the first post-transplant year based on bone mineral density results.

Outcome measures

Outcome measures
Measure
Immunosuppression Without Paricalcitol (Control)
n=42 Participants
Subjects will receive the standard immunosuppressive therapies of Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®), Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
n=41 Participants
Subjects will receive the standard immunosuppressive medications; Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®),Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®), and in addition will receive the study medication paricalcitol (Zemplar®).
Number of Subjects With Osteopenia/Osteoporosis of the Hip at One Year
9 Participants
12 Participants

SECONDARY outcome

Timeframe: 1 year post kidney transplant

Population: Per-protocol analysis; Data were not available for 1 subject from each arm because these subjects did not have the one year DEXA scan of the spine. \[Control n = 43/Treatment n = 42\].

Osteopenia/Osteoporosis are conditions where bone mineral density is lower than normal, reported by T-scores, measurements of the lower spine made using an Dual Energy X-ray Absorptiometry (DEXA) scan. The T-score is measured and compared to a normal healthy adult. A normal bone density results in a T-score between +1.0 and -1.0. A T-score of less than or equal to -1.5 was used for this study to define the presence of osteopenia/osteoporosis. Each participant will be categorized as having or not having osteopenia/osteoporosis of the lumbar spine at the end of the first post-transplant year based on bone mineral density results.

Outcome measures

Outcome measures
Measure
Immunosuppression Without Paricalcitol (Control)
n=43 Participants
Subjects will receive the standard immunosuppressive therapies of Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®), Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
n=42 Participants
Subjects will receive the standard immunosuppressive medications; Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®),Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®), and in addition will receive the study medication paricalcitol (Zemplar®).
Number of Subjects With Osteopenia/Osteoporosis of the Lumbar Spine at One Year
9 Participants
14 Participants

SECONDARY outcome

Timeframe: Baseline, 3 weeks, 3 months, 1 year post kidney transplant

Population: Per-protocol analysis; the number of samples obtained at each time point varied because not all subjects were able to undergo laboratory testing at the specified timepoints. The number of subjects samples per treatment group were as follows \[Timepoint: Control(n)/Treatment(n)\]: Baseline: 43/41, Day 21: 44/41, Day 90: 44/43, Day 365: 44/43

Parathyroid hormone (PTH) is a hormone synthesized in the body's parathyroid glands that controls bone health. PTH controls calcium and phosphorus levels in the body. It is measured in the serum and reported in picograms per milliliter (pg/mL).

Outcome measures

Outcome measures
Measure
Immunosuppression Without Paricalcitol (Control)
n=44 Participants
Subjects will receive the standard immunosuppressive therapies of Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®), Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
n=43 Participants
Subjects will receive the standard immunosuppressive medications; Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®),Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®), and in addition will receive the study medication paricalcitol (Zemplar®).
Serum Parathyroid Hormone (PTH) Level Over Time
Baseline PTH level
236 pg/mL
Interval 50.12 to 1048.0
198 pg/mL
Interval 55.0 to 1266.0
Serum Parathyroid Hormone (PTH) Level Over Time
21 day PTH level
69 pg/mL
Interval 26.0 to 414.0
50 pg/mL
Interval 11.0 to 222.0
Serum Parathyroid Hormone (PTH) Level Over Time
3 month PTH level
70 pg/mL
Interval 34.74 to 273.0
42 pg/mL
Interval 15.0 to 213.0
Serum Parathyroid Hormone (PTH) Level Over Time
1 year PTH level
85 pg/mL
Interval 18.0 to 460.0
42 pg/mL
Interval 12.0 to 266.0

SECONDARY outcome

Timeframe: Baseline, 21 days, 90 days and 1 year post kidney transplant

Population: Per-protocol analysis; the number of samples obtained at each time point varied because not all subjects were able to undergo laboratory testing at the specified study visits. The number of subjects samples per treatment group were as follows \[Timepoint: Control(n)/Treatment(n)\]: Baseline: 43/41, Day 21: 34/38, Day 90: 36/36, Day 365: 43/41

BAP is a marker of bone turn-over, is measured in the serum and reported in micrograms per liter (mcg/L).

Outcome measures

Outcome measures
Measure
Immunosuppression Without Paricalcitol (Control)
n=44 Participants
Subjects will receive the standard immunosuppressive therapies of Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®), Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
n=43 Participants
Subjects will receive the standard immunosuppressive medications; Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®),Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®), and in addition will receive the study medication paricalcitol (Zemplar®).
Serum Bone Alkaline Phosphatase (BAP) Level Over Time
Baseline BAP
14 mcg/L
Interval 6.4 to 34.0
13 mcg/L
Interval 4.9 to 50.0
Serum Bone Alkaline Phosphatase (BAP) Level Over Time
Day 21 BAP
16.5 mcg/L
Interval 6.4 to 81.0
17 mcg/L
Interval 3.8 to 74.0
Serum Bone Alkaline Phosphatase (BAP) Level Over Time
Day 90 BAP
21 mcg/L
Interval 5.8 to 66.0
12 mcg/L
Interval 3.5 to 116.0
Serum Bone Alkaline Phosphatase (BAP) Level Over Time
Day 365 BAP
14 mcg/L
Interval 2.0 to 54.0
11 mcg/L
Interval 4.4 to 100.0

SECONDARY outcome

Timeframe: Baseline, 1 year post kidney transplant

Population: Per-protocol analysis; Not all subjects were able to undergo the DEXA scan of the spine at baseline and one-year \[Control n = 42/Treatment n = 41\].

BMD was measured using a Dual Energy X-ray Absorptiometry (DEXA) scan and reported by T-scores, measurements of the lower spine made using the scan. The T-score reflects how your bone density measurement compares to normal healthy adults. A normal bone density results in a T-score between +1.0 and -1.0. A T-score of less than or equal to -1.5 was used for this study to define the presence of osteopenia/osteoporosis. Osteopenia is a condition of decreased bone mass or density but not thin enough to be diagnosed as osteoporosis. Osteoporosis is a condition where bone mass/density has diminished to a level causing higher risk of fracture. The average change in T-score from baseline to one year is reported.

Outcome measures

Outcome measures
Measure
Immunosuppression Without Paricalcitol (Control)
n=42 Participants
Subjects will receive the standard immunosuppressive therapies of Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®), Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
n=41 Participants
Subjects will receive the standard immunosuppressive medications; Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®),Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®), and in addition will receive the study medication paricalcitol (Zemplar®).
Change in Lumbar Spine Bone Mineral Density (BMD)
0.35 T-score
Standard Deviation 0.45
0.35 T-score
Standard Deviation 0.58

SECONDARY outcome

Timeframe: Baseline, 1 year post kidney transplant

Population: Per-protocol analysis. Not all subjects were able to undergo the DEXA scan of the hip at baseline and one-year \[Control n = 41/Treatment n = 40\].

BMD was measured using a Dual Energy X-ray Absorptiometry (DEXA) scan and reported by T-scores, measurements made of the hip bones using the scan. The T-score reflects how your bone density measurement compares to normal healthy adults. A normal bone density results in a T-score between +1.0 and -1.0. A T-score of less than or equal to -1.5 was used for this study to define the presence of osteopenia/osteoporosis. Osteopenia is a condition of decreased bone mass or density but not thin enough to be diagnosed as osteoporosis. Osteoporosis is a condition where bone mass/density has diminished to a level causing higher risk of fracture. The average change in T-score from baseline to one year is reported.

Outcome measures

Outcome measures
Measure
Immunosuppression Without Paricalcitol (Control)
n=41 Participants
Subjects will receive the standard immunosuppressive therapies of Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®), Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
n=40 Participants
Subjects will receive the standard immunosuppressive medications; Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®),Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®), and in addition will receive the study medication paricalcitol (Zemplar®).
Change in Hip Bone Mineral Density (BMD)
0.15 T-score
Standard Deviation 0.27
0.21 T-score
Standard Deviation 0.36

SECONDARY outcome

Timeframe: Baseline to 1 year post kidney transplant

Population: Per-protocol analysis.

The number of subject who died (or experienced failure of their kidney surgical graft) during the first year following kidney transplant are reported here.

Outcome measures

Outcome measures
Measure
Immunosuppression Without Paricalcitol (Control)
n=44 Participants
Subjects will receive the standard immunosuppressive therapies of Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®), Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
n=43 Participants
Subjects will receive the standard immunosuppressive medications; Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®),Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®), and in addition will receive the study medication paricalcitol (Zemplar®).
Number of Subjects Who Died or Lost Their Renal Graft During First Year
0 participants
1 participants

SECONDARY outcome

Timeframe: Baseline to 1 year post kidney transplant

Population: Per-protocol analysis.

The number of episodes of ACR, as proven by renal biopsy, were recorded.

Outcome measures

Outcome measures
Measure
Immunosuppression Without Paricalcitol (Control)
n=44 Participants
Subjects will receive the standard immunosuppressive therapies of Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®), Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
n=43 Participants
Subjects will receive the standard immunosuppressive medications; Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®),Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®), and in addition will receive the study medication paricalcitol (Zemplar®).
Episodes of Acute Cellular Rejection (ACR) of the Renal Transplant
5 episodes
4 episodes

SECONDARY outcome

Timeframe: 1 year post kidney transplant

Population: Per-protocol analysis

Glomerular filtration rate describes the amount that fluid is filtered through the kidney and can be estimated by using serum creatinine. eGFR is reported in milliliters per minute per 1.73 m\^2 of body-surface area.

Outcome measures

Outcome measures
Measure
Immunosuppression Without Paricalcitol (Control)
n=44 Participants
Subjects will receive the standard immunosuppressive therapies of Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®), Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
n=43 Participants
Subjects will receive the standard immunosuppressive medications; Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®),Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®), and in addition will receive the study medication paricalcitol (Zemplar®).
Mean Estimated Glomerular Filtration Rate (eGFR) at One Year
52.7 mL/min/1.73m^2
Standard Deviation 14.1
51.2 mL/min/1.73m^2
Standard Deviation 15.4

SECONDARY outcome

Timeframe: 3 weeks, 1 year post kidney transplant

Population: Per-protocol analysis

Outcome measures

Outcome measures
Measure
Immunosuppression Without Paricalcitol (Control)
n=44 Participants
Subjects will receive the standard immunosuppressive therapies of Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®), Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
n=43 Participants
Subjects will receive the standard immunosuppressive medications; Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®),Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®), and in addition will receive the study medication paricalcitol (Zemplar®).
Mean Change in Estimated Glomerular Filtration Rate (eGFR) Between 3 Weeks and 1 Year Post Transplant
7.4 mL/min/1.73 m^2
Standard Deviation 15.1
6.2 mL/min/1.73 m^2
Standard Deviation 10.4

SECONDARY outcome

Timeframe: 1 year post kidney transplant

Population: Per-protocol analysis. The 24-hour urine collection was not completed for all subjects.

A urine total protein test is conducted to detect excess protein in the urine. This test helps determine an individual's kidney functioning. Protein is not usually present in urine; therefore, presence of protein in the urine is a sign of abnormality. The quantity of protein in a sample of urine collected over 24-hour was measured and reported in milligrams per day.

Outcome measures

Outcome measures
Measure
Immunosuppression Without Paricalcitol (Control)
n=40 Participants
Subjects will receive the standard immunosuppressive therapies of Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®), Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
n=36 Participants
Subjects will receive the standard immunosuppressive medications; Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®),Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®), and in addition will receive the study medication paricalcitol (Zemplar®).
24-hour Total Protein in the Urine at 1 Year Post Transplant
420.8 mg/day
Standard Deviation 1052.3
159.4 mg/day
Standard Deviation 235.8

SECONDARY outcome

Timeframe: 1 year post kidney transplant

Population: Per-protocol analysis; graft biopsies were not available for all subjects

Interstitial fibrosis refers to degree of scarring or fibrous tissue formed in the kidney. Renal pathologists reviewed biopsies of the subject's kidney grafts for fibrosis, with results expressed using the Banff schema; Quantitative criteria: ci0 = fibrosis observed in up to 5% of cortical area, ci1 = fibrosis in 6%-25% of cortical area (mild) , ci2 = fibrosis in 26%-50% of cortical area (moderate), ci3 = fibrosis in greater than 50% of cortical area (severe). The degree of interstital fibrosis for this study was defined and reported as follows: a Banff ci score of greater than 0 and less than 2 considered "mild" fibrosis and a ci score greater than or equal to 2 as "moderate to severe" fibrosis.

Outcome measures

Outcome measures
Measure
Immunosuppression Without Paricalcitol (Control)
n=38 Participants
Subjects will receive the standard immunosuppressive therapies of Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®), Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
n=38 Participants
Subjects will receive the standard immunosuppressive medications; Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®),Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®), and in addition will receive the study medication paricalcitol (Zemplar®).
Degree of Interstitial Fibrosis on Graft Biopsy at One Year
Mild fibrosis at 1 year
19 Participants
50
19 Participants
50
Degree of Interstitial Fibrosis on Graft Biopsy at One Year
Moderate to severe fibrosis at 1 year
4 Participants
10.5
0 Participants
0

Adverse Events

Immunosuppression Without Paricalcitol (Control)

Serious events: 16 serious events
Other events: 14 other events
Deaths: 0 deaths

Immunosuppression With Paricalcitol

Serious events: 27 serious events
Other events: 32 other events
Deaths: 0 deaths

Serious adverse events

Serious adverse events
Measure
Immunosuppression Without Paricalcitol (Control)
n=49 participants at risk
Subjects will receive the standard immunosuppressive therapies of Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®), Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
n=51 participants at risk
Subjects will receive the standard immunosuppressive medications; Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®),Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®), and in addition will receive the study medication paricalcitol (Zemplar®).
Blood and lymphatic system disorders
neutropenia
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Cardiac disorders
Orthostasis
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Cardiac disorders
myocardial infarction
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Cardiac disorders
atrial fibrillation
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Gastrointestinal disorders
nausea and vomiting
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
General disorders
fever
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
General disorders
headache
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
General disorders
malaise
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Hepatobiliary disorders
liver cirrhosis
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Immune system disorders
allergy to intravenous immunoglobulin
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Metabolism and nutrition disorders
hyperkalemia
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Musculoskeletal and connective tissue disorders
bone fracture
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Musculoskeletal and connective tissue disorders
right leg radicular pain
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
breast cancer
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Neoplasms benign, malignant and unspecified (incl cysts and polyps)
incidental renal cell carcinoma
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Nervous system disorders
seizure
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Psychiatric disorders
depression
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Psychiatric disorders
paranoia
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Renal and urinary disorders
acute kidney injury
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Renal and urinary disorders
hydronephrosis
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
7.8%
4/51 • Number of events 4 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Surgical and medical procedures
bilateral native nephrectomy
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
7.8%
4/51 • Number of events 4 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Surgical and medical procedures
hernia repair
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
7.8%
4/51 • Number of events 4 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Surgical and medical procedures
hysterectomy
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Surgical and medical procedures
motor vehicle accident
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Surgical and medical procedures
ureteral revision
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
3.9%
2/51 • Number of events 2 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Surgical and medical procedures
biopsy complication
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Vascular disorders
pulmonary embolus
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
3.9%
2/51 • Number of events 2 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Vascular disorders
peripheral vascular disease
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
3.9%
2/51 • Number of events 2 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Injury, poisoning and procedural complications
chylous ascitis
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Vascular disorders
vertebral artery dissection
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Injury, poisoning and procedural complications
hematoma
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Injury, poisoning and procedural complications
lymphocele
4.1%
2/49 • Number of events 2 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
3.9%
2/51 • Number of events 2 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Surgical and medical procedures
surgical incision pain
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Injury, poisoning and procedural complications
ureteric revision
4.1%
2/49 • Number of events 2 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
3.9%
2/51 • Number of events 2 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Injury, poisoning and procedural complications
wound complication
4.1%
2/49 • Number of events 2 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
bacteremia
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
Clostridium difficile
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
Cytomegalovirus
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
gastroenteritis
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
pneumonia
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
scrotal cellulitis
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
Turberculosis, Active
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
Upper Respiratory Infection
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
wound infection
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
3.9%
2/51 • Number of events 2 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
Urinary Tract Infection
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
9.8%
5/51 • Number of events 5 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.

Other adverse events

Other adverse events
Measure
Immunosuppression Without Paricalcitol (Control)
n=49 participants at risk
Subjects will receive the standard immunosuppressive therapies of Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®), Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®).
Immunosuppression With Paricalcitol
n=51 participants at risk
Subjects will receive the standard immunosuppressive medications; Alemtuzumab (Campath®), Methylprednisolone (Solumedrol®),Mycophenolate Mofetil (Cellcept®) and Tacrolimus (Prograf®), and in addition will receive the study medication paricalcitol (Zemplar®).
Endocrine disorders
Post transplant diabetes mellitus
4.1%
2/49 • Number of events 2 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
7.8%
4/51 • Number of events 4 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Gastrointestinal disorders
diarrhea
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
5.9%
3/51 • Number of events 3 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Immune system disorders
allergy to Bactrim
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Metabolism and nutrition disorders
gout
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Metabolism and nutrition disorders
symptomatic hypomagnesemia
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Musculoskeletal and connective tissue disorders
Fall in bathroom
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Surgical and medical procedures
Re-operation
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.2%
1/46 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
viral (BK) nephropathy
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
BK viremia
8.2%
4/49 • Number of events 4 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
pyelonephritis
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
Herpes Zoster
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
pneumonia
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
sinusitis
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
Cytomegalovirus viremia
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
3.9%
2/51 • Number of events 2 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
Clostridium difficile
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Renal and urinary disorders
bladder urgency
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Renal and urinary disorders
glomerulonephritis
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Surgical and medical procedures
Surgical Incision Pain
2.0%
1/49 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Infections and infestations
Urinary Tract Infections
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
19.6%
10/51 • Number of events 11 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Injury, poisoning and procedural complications
Wound Complication
6.1%
3/49 • Number of events 3 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
0.00%
0/51 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
Cardiac disorders
Atrial Fibrillation
0.00%
0/49 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.
2.0%
1/51 • Number of events 1 • Adverse events were monitored and collected from baseline to 52 weeks post kidney transplant.
Adverse events were determined based on changes in clinical symptoms and changes in laboratory results at various timepoints and during study visits. Mayo Clinic management programs currently in place for renal transplant recipients with specific laboratory abnormalities were used to diagnose and manage conditions.

Additional Information

Hatem Amer, MD, FASN; Assistant Professor of Medicine; Division of Nephrology and Hypertension

Mayo Clinic

Phone: 507-256-1963

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place

Restriction type: LTE60