drugset / Trial / NCT06393361

Chidamide Decitabine Plus Anti-PD-1 Antibody for Patients With R/R cHL Who Are Transplant-ineligible or Refused Transplant.

NCT06393361

Phase 2 Recruiting 100 enrolled Chinese PLA General Hospital
RandomizedParallel-groupOpen-labelTreatment

Summary

The prognosis for patients with relapsed/refractory classical Hodgkin lymphoma (cHL) who refuse or are ineligible for transplant is poor. This open label, randomized, phase 2 study aims to evaluate the efficacy of Chidamide+Decitabine plus Anti-PD-1 Antibody and Brentuximab Vedotin plus Anti-PD-1 Antibody in transplant-ineligible or refused transplant diagnosedR/R cHL. The primary objective of the study is to evaluate progression-free survival.

Timeline

Start
2024-06-01
Primary completion
2027-06-01
Completion
2027-06-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator Brentuximab Vedotin Monoclonal antibody 1.8 mg/kg
Subject Decitabine Small molecule 10 mg
Subject Tucidinostat Small molecule 20 mg Oral