drugset / Trial / NCT05873907

A Study to Evaluate the Safety, Tolerability, Immunogenicity, Pharmacokinetics, and Pharmacodynamics of AMG 592 in Healthy Participants

NCT05873907 ↗

Phase 1 Completed 64 enrolled Amgen
RandomizedParallel-groupDouble-blindBasic science

Summary

The primary objective of this study is to evaluate the safety, tolerability and immunogenicity profile of single and multiple dose administrations of AMG 592 in healthy participants.

Timeline

Start
2015-10-19
Primary completion
2017-06-16
Completion
2017-07-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Efavaleukin alfa Protein / enzyme biologic — Subcutaneous