drugset / Trial / NCT05389462
A Study of Mipasetamab Uzoptirine (ADCT-601) in Participants With Solid Tumors
Non-randomizedSequentialOpen-labelTreatment
Summary
The primary objective of this study is to identify the recommended phase 2 dose (RP2D) and/or the maximum tolerated dose (MTD), and characterize the safety and tolerability of ADCT-601 monotherapy and in combination with gemcitabine.
Timeline
- Start
- 2022-07-13
- Primary completion
- 2025-04-17
- Completion
- 2025-04-17
Outcome
Outcome not reported
Stopped: “Sponsor decided to halt further development of ADCT-601”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Gemcitabine | Small molecule | — | Intravenous |
| Subject | MIPASETAMAB UZOPTIRINE | Unknown | — | Intravenous |