drugset / Trial / NCT02961101

Anti-PD-1 Antibody Alone or in Combination With Decitabine/Chemotherapy in Relapsed or Refractory Malignancies

NCT02961101

Phase 1/2 Recruiting 250 enrolled Han weidong
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the feasibility, safety, and efficacy of anti-PD-1 antibody alone or in combination with low-dose decitabine in patients with relapsed or refractory malignancies, including Non-Hodgkin'lymphoma, Hodgkin'lymphoma, gastrointestinal cancers, hepatocellular carcinoma, breast cancer, ovarian cancer or lung cancer or renal-cell cancer or pancreatic cancer or bile duct cancer.

Timeline

Start
2016-05
Primary completion
2026-05
Completion
2026-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Camrelizumab Monoclonal antibody 1 mg/kg Intravenous
Subject Camrelizumab Monoclonal antibody 3 mg/kg Intravenous
Subject Camrelizumab Monoclonal antibody 200 mg Intravenous
Subject Decitabine Small molecule 10 mg Intravenous

Indications