drugset / Trial / NCT03146416

Study of Evinacumab (REGN1500) in Caucasian and in Japanese Healthy Volunteers

NCT03146416 ↗

Phase 1 Completed 96 enrolled Regeneron Pharmaceuticals
RandomizedSequentialTriple-blindBasic science

Summary

The primary objective of the study is to compare the safety and tolerability of subcutaneous (SC) and intravenous (IV) doses of evinacumab in healthy Japanese and Caucasian subjects.

Timeline

Start
2017-05-16
Primary completion
2018-06-14
Completion
2018-06-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Evinacumab Monoclonal antibody — Subcutaneous

Indications

No indication recorded.