drugset / Trial / NCT07450521

Evaluation of MTX-463 Administered Subcutaneously in Healthy Adult Males

NCT07450521 ↗

Phase 1 Completed 8 enrolled Mediar Therapeutics
RandomizedParallel-groupQuadruple-blindOther

Summary

A randomized, double-blind, placebo-controlled, study to assess the safety, tolerability, and PK of MTX-463 when administered via SC injection in healthy adult males.

Timeline

Start
2026-02-18
Primary completion
2026-03-11
Completion
2026-03-11

Drugs

EvaluationDrugModalityDoseRoute
Subject MTX-463 Monoclonal antibody 250 mg Subcutaneous

Indications

No indication recorded.