drugset / Trial / NCT06462794

First In Human Study of CX-801 in Advanced Solid Tumors

NCT06462794 ↗

Phase 1 Recruiting 121 enrolled CytomX Therapeutics Merck Sharp & Dohme LLC · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

The purpose of this first-in-human study, CTMX-801-101, is to characterize the safety, tolerability, and antitumor activity of CX-801 as monotherapy and in combination with pembrolizumab in adult participants with advanced solid tumors.

Timeline

Start
2024-08-28
Primary completion
2028-02-28
Completion
2029-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject CX-801 Unknown — —
Background Pembrolizumab Monoclonal antibody — —

Indications