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Ascending Dose Study of the Safety and Tolerability of REGN6490 in Healthy Volunteers

Healthy Volunteer Clinical Trial

Official title:
A Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose Study of the Safety, Tolerability and Pharmacokinetics of REGN6490 in Healthy Volunteers

Clinical Trial Summary

The primary objective of the study is to evaluate the safety and tolerability of single ascending intravenous (IV) and subcutaneous (SC) doses of REGN6490 in healthy adult participants The secondary objectives of the study are to: - Characterize the pharmacokinetic (PK) profile of single IV and SC doses of REGN6490 in healthy adult participants - Assess immunogenicity of REGN6490 in healthy adult participants dosed with a single IV or SC dose of REGN6490

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04616079
Study type Interventional
Source Regeneron Pharmaceuticals
Contact
Status Terminated
Phase Phase 1
Start date November 19, 2020
Completion date June 1, 2021
View Details
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