drugset / Trial / NCT06797336
A Study of PT0253 in Participants With KRAS G12D Mutated Advanced Solid Tumors
RandomizedSequentialOpen-labelTreatment
Summary
The primary purpose of this study is to evaluate the safety and tolerability, determine the maximally tolerated dose (MTD) and/or recommended Phase 2 dose(s) (RP2D) of PT0253 in adult participants with Kirsten rat sarcoma viral oncogene homolog (KRAS) G12D mutated advanced solid tumors as monotherapy.
Timeline
- Start
- 2024-12-19
- Primary completion
- 2026-12-15
- Completion
- 2027-06-16
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PT0253 | Unknown | — | Intravenous |