drugset / Trial / NCT04924413
L-TIL Plus Tislelizumab as First-line Treatment in Advanced Malignant Melanoma
NaSingle-groupOpen-labelTreatment
Summary
The main purpose of this study is to evaluate the safety and effectiveness of liquid tumor infiltrating lymphocytes (L-TIL) combined with tislelizumab as the first-line treatment in patients with advanced malignant melanoma. This study plan to include stage III or IV unresectable or metastatic cutaneous or acral malignant melanoma patients, treat with L-TIL 4 cycles with each infusion (3 -10) x10\*9/m2 cells, combined with tislelizumab 200mg, iv, Q3W. It is expected that 30 patients will be enrolled in this study.
Timeline
- Start
- 2021-07-01
- Primary completion
- 2024-07-02
- Completion
- 2024-07-02
Outcome
Outcome not reported
Stopped (Enrollment): “Slow enrollment”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Tislelizumab | Monoclonal antibody | 200 mg | Intravenous |
| Subject | liquid tumor infiltrating lymphocytes | Cell therapy | — | Other |