Efficacy and Safety of Etelcalcetide (AMG 416) in the Treatment of Secondary Hyperparathyroidism (SHPT) in Patients With Chronic Kidney Disease (CKD) on Hemodialysis



Status:Completed
Conditions:Renal Impairment / Chronic Kidney Disease, Endocrine
Therapuetic Areas:Endocrinology, Nephrology / Urology
Healthy:No
Age Range:18 - 100
Updated:9/2/2018
Start Date:March 12, 2013
End Date:May 9, 2014

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A Randomized, Double-blind, Placebo-controlled, Phase 3 Study to Assess the Efficacy and Safety of AMG 416 in the Treatment of Secondary Hyperparathyroidism in Subjects With Chronic Kidney Disease on Hemodialysis

This study is designed to assess the efficacy and safety of etelcalcetide (AMG 416) compared
with placebo in the treatment of SHPT in CKD patients receiving hemodialysis.


Inclusion Criteria:

- Subject understands the study procedures and agrees to participate in the study by
giving written informed consent.

- Subject is 18 years of age or older.

- Subject agrees to not participate in another study of an investigational agent during
the study.

- Subject must be receiving hemodialysis 3 times weekly for at least 3 months

- Other Inclusion Criteria may apply

Exclusion Criteria:

- Currently receiving treatment in another investigational device or drug study, or
ended treatment on another investigational device or drug study(s) within 8 weeks
prior to screening.

- Other investigational procedures while participating in this study are excluded.

- Anticipated or scheduled parathyroidectomy during the study period.

- Subject has received a parathyroidectomy within 3 months prior to dosing.

- Anticipated or scheduled kidney transplant during the study period.

- Subject has known sensitivity to any of the products or components to be administered
during dosing.

- Subject has participated in a prior clinical trial of AMG 416

- Subject has an unstable medical condition based on medical history, physical
examination, and routine laboratory tests, or is otherwise unstable in the judgment of
the Investigator.

- Subject has a history of any illness that, in the opinion of the Investigator, might
confound the results of the study or pose additional risk to the subject.

- Other Exclusion Criteria may apply
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