drugset / Trial / NCT03247309
TCR-engineered T Cells in Solid Tumors (ACTengine IMA201-101)
NaSingle-groupOpen-labelTreatment
Summary
The study purpose is to establish the safety and tolerability of IMA201 in patients with solid tumors that express melanoma-associated antigen 4 and/or 8 (MAGEA4/8).
Timeline
- Start
- 2018-12-19
- Primary completion
- 2023-04-20
- Completion
- 2023-09-18
Outcome
Results reported · no primary-endpoint met/missed verdict (typical of a dose-finding / safety study)
release “The combined data readout during early phases of dose escalation for the ACTengine ® programs, IMA201, IMA202 and IMA203, indicated first anti-tumor activity” immatics.com ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | IMA201 | Unknown | — | Intravenous |