drugset / Trial / NCT05481411

A Study to Evaluate the Pharmacokinetics, Safety, and Pharmacodynamics of Olpasiran in Participants With Various Degrees of Hepatic Impairment

NCT05481411 ↗

Phase 1 Completed 25 enrolled Amgen
Non-randomizedParallel-groupOpen-labelBasic science

Summary

The primary objective of the study is to evaluate the pharmacokinetics (PK) of a single dose of olpasiran in participants with mild, moderate, or severe hepatic impairment compared to participants with normal hepatic function.

Timeline

Start
2022-09-13
Primary completion
2023-04-05
Completion
2023-05-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Olpasiran Unknown — Subcutaneous

Indications

No indication recorded.