drugset / Trial / NCT06520488

A Study of HRS-4642 in Combination With Antineoplastic Agents in Advanced Solid Tumors

NCT06520488

Phase 1/2 Recruiting 118 enrolled Jiangsu HengRui Medicine Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

To evaluate the safety and preliminary efficacy of HRS-4642 in combination with antineoplastic agents in subjects with advanced solid tumors with KRAS G12D mutations, and to determine the maximum tolerated dose (MTD) and the recommended Phase II dose (RP2D).

Timeline

Start
2024-08-09
Primary completion
2027-03
Completion
2027-07

Drugs

EvaluationDrugModalityDoseRoute
Subject HRS-4642 Unknown 1200 mg Intravenous

Indications