drugset / Trial / NCT03502330

APX005M With Nivolumab and Cabiralizumab in Advanced Melanoma, Non-small Cell Lung Cancer or Renal Cell Carcinoma

NCT03502330

Non-randomizedSingle-groupOpen-labelTreatment

Summary

This trial is a phase 1/1b study to evaluate the safety, efficacy, and tolerability of APX005M in combination with nivolumab and cabiralizumab. The phase 1 dose escalation portion of the study will enroll patients with advanced solid tumors melanoma, non-small cell lung cancer (NSCLC), and renal cell carcinoma (RCC) in 6 cohorts to determine the recommended phase II dose (RP2D) of APX005M. The phase 1b dose expansion portion will study the triple drug combination separately in the three disease cohorts: melanoma, NSCLC, and RCC.

Timeline

Start
2018-06-09
Primary completion
2022-01-05
Completion
2024-05-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Cabiralizumab Monoclonal antibody 4 mg/kg Intravenous
Subject Nivolumab Monoclonal antibody 240 mg Intravenous
Subject sotigalimab Monoclonal antibody 0.03 mg/kg Intravenous
Subject sotigalimab Monoclonal antibody 0.1 mg/kg Intravenous
Subject sotigalimab Monoclonal antibody 0.3 mg/kg Intravenous