drugset / Trial / NCT02994953

A Phase Ib Study to Evaluate the Safety, Tolerability, and Pharmacokinetics (PK) of Avelumab in Combination With M9241(NHS-IL12) (JAVELIN IL-12)

NCT02994953

Non-randomizedSequentialOpen-labelTreatment

Summary

The study consisted of 2 parts: Dose Escalation phase (Part A) and Expansion phase (Part B). The dose escalation phase evaluated the safety, tolerability, and PK of avelumab in combination with M9241 in subjects with locally advanced, unresectable, or metastatic solid tumors. Expansion phase assessed the safety and clinical activity of the combination regimen in selected tumor types. In Expansion phase subjects who had completed the combination treatment of avelumab at a given dose level of M9241, a safety review was performed by the Safety monitoring committee in order to make a decision on the next dose level. Successive cohorts of 3 to 6 subjects were treated with escalating doses of M9241 with avelumab intravenous (IV).

Timeline

Start
2017-01-31
Primary completion
2020-10-08
Completion
2020-10-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Avelumab Monoclonal antibody 10 mg/kg Intravenous
Subject Avelumab Monoclonal antibody 800 mg Intravenous
Subject NHS-IL12 Protein / enzyme biologic 4 ug/kg Subcutaneous
Subject NHS-IL12 Protein / enzyme biologic 8 ug/kg Subcutaneous
Subject NHS-IL12 Protein / enzyme biologic 12 ug/kg Subcutaneous
Subject NHS-IL12 Protein / enzyme biologic 16.8 ug/kg Subcutaneous

Indications