drugset / Trial / NCT04924413

L-TIL Plus Tislelizumab as First-line Treatment in Advanced Malignant Melanoma

NCT04924413 ↗

Phase 2 Terminated 9 enrolled Quanli Gao
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

EvaluationDrugModalityDoseRoute
Subject Tislelizumab Monoclonal antibody 200 mg Intravenous
Subject liquid tumor infiltrating lymphocytes Cell therapy — Other

Indications