drugset / Trial / NCT06829225

Single Dose Study of Tulisokibart (MK-7240) in Healthy Chinese Participants (MK-7240-002)

NCT06829225 ↗

Phase 1 Completed 48 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupTriple-blindBasic science

Summary

The goal of this study is to learn about the safety of tulisokibart in healthy participants and what happens to tulisokibart over time when participants receive treatment intravenously versus subcutaneously.

Timeline

Start
2024-06-13
Primary completion
2024-11-11
Completion
2024-11-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Tulisokibart Monoclonal antibody — Subcutaneous

Indications