Solid Tumor Clinical Trial
Official title:
A Phase 1/2 Study to Assess Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of TU2218, an Oral TGFβR Inhibitor, Administered Alone and in Combination With Pembrolizumab in Patients With Advanced Solid Tumors
This study consists of Part A for monotherapy and Part B for combination therapy to evaluate safety, tolerability, pharmacokinetics, and preliminary efficacy of TU2218 in patients with advanced solid tumors. The main purpose of Phase 1 is to determined the recommended Phase 2 dose (RP2D) of TU2218 and the main purpose of Phase 2 is to evaluate the antitumor activity of TU2218 at RP2D.
n/a
| NCT number | NCT05204862 |
| Study type | Interventional |
| Source | TiumBio Co., Ltd. |
| Contact | TiumBio Global http://www.tiumbio.com/en/ |
| Phone | 82-31-600-1500 |
| [email protected] | |
| Status | Recruiting |
| Phase | Phase 1/Phase 2 |
| Start date | December 2, 2021 |
| Completion date | September 30, 2027 |
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