drugset / Trial / NCT07526116

A First in Human Study to Assess Safety, Tolerability and Pharmacokinetics of a Single Dose of REGN22044 in Healthy Adults

NCT07526116 ↗

Phase 1 Not yet recruiting 64 enrolled Regeneron Pharmaceuticals
RandomizedSequentialQuadruple-blindTreatment

Summary

This clinical study will evaluate the study drug, REGN22044, in healthy participants. REGN22044 has not previously been studied in humans. The purpose of this study is to learn: * What side effects may happen when REGN22044 is taken * How much of REGN22044 is in the blood at different times * Whether the body makes antibodies against REGN22044 (which could make the drug less effective or could lead to side effects)

Timeline

Start
2026-05-07
Primary completion
2027-05-27
Completion
2027-05-27

Drugs

EvaluationDrugModalityDoseRoute
Subject REGN22044 Unknown — Intravenous

Indications

No indication recorded.