drugset / Trial / NCT06971523
A Phase I/II Clinical Study of CTS3497 in Patients With MTAP Deficient Malignacies
Non-randomizedSequentialOpen-labelTreatment
Summary
The primary objective of Phase I of this study is to evaluate the safety and tolerability, and to determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D) of CTS3497 in patients with metastatic or locally advanced methylthioadenosine phosphorylase (MTAP)-deficient solid tumors and lymphomas. The primary objective of Phase II of this study is to evaluate the efficacy of CTS3497 in patients with metastatic or locally advanced MTAP-deficient solid tumors and lymphomas.
Timeline
- Start
- 2024-12-25
- Primary completion
- 2028-12-31
- Completion
- 2029-06-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | CTS3497 | Unknown | — | Oral |