drugset / Trial / NCT06520488
A Study of HRS-4642 in Combination With Antineoplastic Agents in Advanced Solid Tumors
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | HRS-4642 | Unknown | 1200 mg | Intravenous |