drugset / Trial / NCT07646353

First-in-Human Dose-escalation of GSK4425689A: Safety, Tolerability, and PK in Healthy Adults

NCT07646353 ↗

Phase 1 Not yet recruiting 40 enrolled GlaxoSmithKline
RandomizedSequentialQuadruple-blindPrevention

Summary

This study will assess the safety, tolerability, and pharmacokinetic properties of GSK4425689A monoclonal antibody (mAb) in healthy adults, when administered by either intravenous (IV) or subcutaneous (SC) routes.

Timeline

Start
2026-06-12
Primary completion
2028-04-19
Completion
2028-04-19

Drugs

EvaluationDrugModalityDoseRoute
Subject GSK4425689A Monoclonal antibody — Subcutaneous