drugset / Trial / NCT01833754

Study of Romosozumab (AMG 785) Administered to Healthy Participants and Patients With Stage 4 Renal Impairment or Stage 5 Renal Impairment Requiring Hemodialysis

NCT01833754

Phase 1 Completed 24 enrolled Amgen
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety, tolerability, and immunogenicity profile of romosozumab after a single 210 mg subcutaneous dose in healthy participants and patients with stage 4 renal impairment (RI) or stage 5 RI requiring hemodialysis.

Timeline

Start
2013-04-22
Primary completion
2014-02-19
Completion
2014-02-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Romosozumab Monoclonal antibody 210 mg Subcutaneous

Indications