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

Completed · Phase 3 · Has a placebo group

Conditions studied: Hyperparathyroidism, Secondary

In brief

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

Key facts

Study ID

NCT01785849

Run by

Amgen

People needed

508

Starts

2013-03-12

Expected to finish

2014-06-12

Last updated by the study team

2019-08-26

Who can join

Age: 18 and older, up to 100. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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 must be receiving hemodialysis 3 times weekly for at least 3 months
• Subject agrees to not participate in another study of an investigational agent during the study.
• Other Inclusion Criteria may apply

You may not qualify if…

• 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 (also referred to as KAI-4169).
• Subject has received cinacalcet within the 4 weeks prior to screening labs (treatment with cinacalcet is prohibited during the study).
• 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.
• Other Exclusion Criteria may apply

Where it is running

• Research Site — Pine Bluff, Arkansas, United States
• Research Site — Azusa, California, United States
• Research Site — Covina, California, United States
• Research Site — Lakewood, California, United States
• Research Site — Los Angeles, California, United States
• Research Site — Lynwood, California, United States
• Research Site — Northridge, California, United States
• Research Site — Ontario, California, United States
• Research Site — Panorama City, California, United States
• Research Site — Sacramento, California, United States
• Research Site — Whittier, California, United States
• Research Site — Pembroke Pines, Florida, United States
• Research Site — Meridian, Idaho, United States
• Research Site — Evanston, Illinois, United States
• Research Site — Springfield, Massachusetts, United States
• Research Site — Detroit, Michigan, United States
• Research Site — Kalamazoo, Michigan, United States
• Research Site — Pontiac, Michigan, United States
• Research Site — Southgate, Michigan, United States
• Research Site — Tupelo, Mississippi, United States
• Research Site — Kansas City, Missouri, United States
• Research Site — Reno, Nevada, United States
• Research Site — Amherst, New York, United States
• Research Site — Brooklyn, New York, United States
• Research Site — Birmingham, Alabama, United States

Full record on ClinicalTrials.gov

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