drugset / Trial / NCT05394103

Highly Selective CDK7 Inhibitor Q901 in Selected Advanced Solid Tumors

NCT05394103 ↗

Phase 1/2 Recruiting 130 enrolled Qurient Co., Ltd. Merck Sharp & Dohme LLC · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

Multicenter, open-label, dose-escalation, safety, tolerability, PK and pharmacodynamic study with a dose expansion at the RP2D to evaluate safety and potential antitumor activity of Q901 as a monotherapy and in combination with pembrolizumab

Timeline

Start
2022-08-30
Primary completion
2025-12-30
Completion
2026-08-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Pembrolizumab Monoclonal antibody — —
Subject Q901 Unknown — Intravenous