drugset / Trial / NCT04050462

Nivolumab Combined With BMS-986253 in HCC Patients

NCT04050462 ↗

Phase 2 Terminated 13 enrolled NYU Langone Health
RandomizedParallel-groupOpen-labelTreatment

Summary

A phase II clinical trial is utilized to examine whether BMS-986253 (25 subjects) or Cabiralizumab (25 subjects) when combined with Nivolumab offers improved radiographic objective response rates (ORR) over Nivolumab monotherapy (25 subjects) in advanced HCC patients.

Timeline

Start
2019-09-12
Primary completion
2025-01-31
Completion
2025-01-31

Outcome

Outcome not reported

Stopped (Enrollment): “Study was terminated early by the drug sponsor due to slow accrual and a change in the company's drug development priorities”

Drugs

EvaluationDrugModalityDoseRoute
Subject ADAKITUG Monoclonal antibody 1200 mg Intravenous
Subject Cabiralizumab Monoclonal antibody 4 mg/kg Intravenous
Subject Nivolumab Monoclonal antibody 240 mg Intravenous