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Phase 3 N=213 Randomized Double-blind Treatment

Safety and Efficacy of CTAP101 to Treat Secondary Hyperparathyroidism in Stage 3 or 4 CKD and Vitamin D Insufficiency

Chronic Kidney Disease · Hyperparathyroidism, Secondary · Vitamin D Deficiency

Enrolled (actual)
213
Serious AEs
19.7%
Results posted
Aug 2016
Primary outcome: Primary: Number of Participants in the Intent to Treat Population With Decrease in Plasma Intact Parathyroid Hormone (iPTH) of ≥30% From Pre-treatment Baseline Values — 6; 46 participants — p=<0.0001

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
CTAP101 30 μg capsules (Drug); Sugar pill to CTAP101 30 μg capsules (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
OPKO IP Holdings II, Inc.
Primary completion
Jul 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants in the Intent to Treat Population With Decrease in Plasma Intact Parathyroid Hormone (iPTH) of ≥30% From Pre-treatment Baseline Values
6; 46 <0.0001 sig
SECONDARY
Number of Participants in the Per Protocol Population With Decrease in Plasma Intact Parathyroid Hormone (iPTH) of ≥30% From Pre-treatment Baseline Values
5; 46 <0.0001 sig
SECONDARY
Subjects in the Intent to Treat Population With Normal Serum Total 25-hydroxyvitamin D
2; 113 <0.0001 sig
SECONDARY
Subjects in the Per Protocol Population With Normal Serum Total 25-hydroxyvitamin D
2; 110

Summary

This study will evaluate the efficacy of CTAP101 Capsules versus placebo in reducing intact parathyroid hormone (iPTH) by at least 30% from pretreatment baseline; safety and tolerability of CTAP101 will also be evaluated

Eligibility Criteria

Inclusion Criteria

  • Urinary albumin excretion ≤ 3000 mcg/mg of creatinine
  • Stage 3 or 4 CKD
  • Plasma iPTH: ≥ 85 pg/mL and 0.2 (>200 mg/g Cr)
  • Current serious illness, such as malignancy, HIV, liver disease, cardiovascular event or hepatitis
  • Currently on dialysis
  • Use of pharmacological dose of ergocalciferol or cholecalciferol (≥ 50,000 IU mcg per month) during the study
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01651000). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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