drugset / Trial / NCT02671435

A Study of Durvalumab (MEDI4736) and Monalizumab in Solid Tumors

NCT02671435

Phase 1/2 Active not recruiting 383 enrolled MedImmune LLC
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a multicenter, open-label, dose-escalation, dose-exploration and dose-expansion study to evaluate the safety, tolerability, antitumor activity, pharmacokinetic (PK), pharmacodynamics, and immunogenicity of durvalumab (MEDI4736) in combination with monalizumab (IPH2201) in adult participants with selected advanced solid tumors and the combination of durvalumab and monalizumab (IPH2201) standard of care systemic therapy with or without biological agent and monalizumab (IPH2201) with biological agent administered to participants with recurrent or metastatic colorectal cancer (CRC).

Timeline

Start
2016-02-22
Primary completion
2021-10-26
Completion
2027-07-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Durvalumab Monoclonal antibody 1500 mg Intravenous
Subject Monalizumab Monoclonal antibody 22.5 mg Intravenous
Subject Monalizumab Monoclonal antibody 75 mg Intravenous
Subject Monalizumab Monoclonal antibody 225 mg Intravenous
Subject Monalizumab Monoclonal antibody 750 mg Intravenous
Background Bevacizumab Monoclonal antibody 5 mg/kg Intravenous
Background Cetuximab Monoclonal antibody 500 mg/m2 Intravenous
Background Leucovorin Small molecule 400 mg/m2
Background Oxaliplatin Small molecule 85 mg/m2 Intravenous
Background fluorouracil Small molecule 400 mg/m2 Intravenous
Background fluorouracil Small molecule 2400 mg/m2 Intravenous

Indications