drugset / Trial / NCT05923424

A Trial to Learn if Different Doses of REGN17092 Are Safe in Healthy Adults

NCT05923424 ↗

Phase 1 Completed 40 enrolled Regeneron Pharmaceuticals
RandomizedSequentialQuadruple-blindTreatment

Summary

The purpose of this study is to learn about the safety and tolerability of different doses of REGN17092 administered with a needle either under the skin (called "subcutaneous") or into a vein (called an "infusion") in healthy participants. This is the first time that REGN17092 will be given to people. Other aims are to assess: * How much of the study drug is in the blood at different times * Whether the body makes its own antibodies against the study drug (which could make the drug less effective or lead to side effects)

Timeline

Start
2023-11-28
Primary completion
2025-03-04
Completion
2025-03-04

Drugs

EvaluationDrugModalityDoseRoute
Subject REGN17092 Monoclonal antibody — Intravenous

Indications

No indication recorded.