Safety and Efficacy of Hectorol in Pediatric Patients With Chronic Kidney Disease Stage 3 and 4 With Secondary Hyperparathyroidism Not Yet on Dialysis
Status: | Recruiting |
---|---|
Conditions: | Renal Impairment / Chronic Kidney Disease, Endocrine |
Therapuetic Areas: | Endocrinology, Nephrology / Urology |
Healthy: | No |
Age Range: | 5 - 18 |
Updated: | 3/27/2019 |
Start Date: | January 19, 2017 |
End Date: | April 2, 2020 |
Contact: | Trial Transparency email recommended (Toll free number for US & Canada) |
Email: | Contact-Us@sanofi.com |
Phone: | 800-633-1610 |
An Open-Label, Randomized, Parallel Group Study to Assess the Safety and Efficacy of Hectorol® (Doxercalciferol Capsules) in Pediatric Patients With Chronic Kidney Disease Stages 3 and 4 With Secondary Hyperparathyroidism Not Yet on Dialysis
Primary Objective:
Evaluate the effect of Hectorol® capsules in reducing elevated levels of intact parathyroid
hormone (iPTH).
Secondary Objectives:
- Evaluate the safety profile of Hectorol® capsules versus Rocaltrol® (calcitriol)
capsules.
- Determine the pharmacokinetic profile of 1,25-dihydroxyvitamin D2 after administration
of Hectorol®.
Evaluate the effect of Hectorol® capsules in reducing elevated levels of intact parathyroid
hormone (iPTH).
Secondary Objectives:
- Evaluate the safety profile of Hectorol® capsules versus Rocaltrol® (calcitriol)
capsules.
- Determine the pharmacokinetic profile of 1,25-dihydroxyvitamin D2 after administration
of Hectorol®.
The total study duration per patient will be approximately up to 28 weeks.
Inclusion criteria :
- Male or female aged 5 to 18 years old.
- Weight ≥15 kg.
- Chronic kidney disease (CKD) Stage 3 or 4 not on dialysis, defined as glomerular
filtration rate (GFR) between 15 and 59 mL/min/1.73m^2 (established by Schwartz
equation) at Week -2 visit.
- Intact parathyroid hormone (iPTH) value >100 pg/mL for CKD Stage 3 or >160 pg/mL for
CKD Stage 4, at Week -2 visit.
- Signed informed consent/assent form.
Exclusion criteria:
- The patient has a serum 25-hydroxyvitamin D level <30 ng/mL at screening.
- The patient has a corrected calcium ≥10 mg/dL at the Week -2 visit.
- The patient has a serum phosphorus >4.5 mg/dL for children 13 to 18 years of age; >5.8
mg/dL for children 5 to 12 years of age at the Week -2 visit.
- The patient is anticipated to require maintenance hemodialysis within 3 months.
- The patient used cinacalcet or vitamin D sterol therapies such as calcitriol,
doxercalciferol, or paricalcitol within 14 days prior to the baseline visit.
- The patient has a history of, or active, symptomatic heart disease within 12 months
prior to the baseline (Week 0) visit.
- The patient currently has a chronic gastrointestinal disease (ie, malabsorption,
severe chronic diarrhea, chronic ulcerative colitis, or ileostomy).
- The patient currently has primary hyperparathyroidism or has had a total
parathyroidectomy.
- The patient has an active malignancy.
- The patient is unable to swallow a capsule in size similar to the Hectorol® and
Rocaltrol® capsules.
- The patient has a history of sensitivity or allergy to doxercalciferol, calcitriol or
other vitamin D analogs.
- The patient currently uses aluminum or magnesium-based binders.
The above information is not intended to contain all considerations relevant to a patient's
potential participation in a clinical trial.
We found this trial at
29
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