drugset / Trial / NCT05725291

AMT-116 in Patients With Advanced Solid Tumors

NCT05725291

Phase 1 Recruiting 80 enrolled Multitude Therapeutics Inc.
NaSingle-groupOpen-labelTreatment

Summary

This first-in-human study will evaluate the Maximum Tolerated Dose (MTD) / the Recommended Phase 2 Dose (RP2D), safety, tolerability, anti-tumor activity, pharmacokinetics, pharmacodynamics and immunogenicity of AMT-116, in Patients with Advanced Solid Tumors

Timeline

Start
2023-07-25
Primary completion
2026-12-30
Completion
2026-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject AMT-116 Other / unclassified Intravenous

Indications