drugset / Trial / NCT02668770

Ipilimumab (Immunotherapy) and MGN1703 (TLR Agonist) in Patients With Advanced Solid Malignancies

NCT02668770

Phase 1 Terminated 28 enrolled M.D. Anderson Cancer Center Mologen AG · collab
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The goal of this clinical research study is to find the highest tolerable dose of MGN1703 that can be given in combination with ipilimumab to patients with advanced tumors. The safety of this drug combination will also be studied. This is an investigational study. MGN1703 is not FDA approved or commercially available. It is currently being used for research purposes only. Ipilimumab is FDA approved and commercially available for the treatment of unresectable (cannot be removed with surgery) or metastatic (has spread) melanoma. Up to 60 participants will be enrolled in this study. All will take part at MD Anderson.

Timeline

Start
2016-05-11
Primary completion
2025-11-05
Completion
2025-11-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Ipilimumab Monoclonal antibody 3 mg/kg Intravenous
Subject lefitolimod Oligonucleotide (other) 15 mg Subcutaneous
Subject lefitolimod Oligonucleotide (other) 120 mg Subcutaneous