drugset / Trial / NCT07502768

Tislelizumab Plus Zeprumetostat for Relapsed or Refractory NK/T-Cell Lymphoma

NCT07502768

Phase 1/2 Recruiting 107 enrolled Rong Tao Fudan University · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a multicenter, open-label, phase Ib/II study evaluating tislelizumab in combination with zeprumetostat (SHR2554) in patients with relapsed or refractory NK/T-cell lymphoma after at least one prior asparaginase-based chemotherapy-containing regimen, with or without radiotherapy. In phase Ib, two fixed dose levels of zeprumetostat in combination with tislelizumab will be evaluated to determine the recommended phase II dose (RP2D). In phase II, patients will be enrolled into 2 predefined cohorts according to prior exposure to PD-1 inhibitors to further evaluate efficacy and safety. The primary phase II endpoint is objective response rate at week 12 assessed by independent blinded imaging review according to Lugano 2014 criteria.

Timeline

Start
2026-04-30
Primary completion
2027-12-30
Completion
2028-12-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Tislelizumab Monoclonal antibody 200 mg Intravenous
Subject Zeprumetostat Small molecule 300 mg Oral
Subject Zeprumetostat Small molecule 350 mg Oral