drugset / Trial / NCT01447225

Safety Study of MM-121 in Combination With Multiple Anticancer Therapies in Patients With Advanced Solid Tumors

NCT01447225

Phase 1 Completed 43 enrolled Merrimack Pharmaceuticals Sanofi · collab
Non-randomizedParallel-groupOpen-labelTreatment

Summary

To evaluate the safety and tolerability of escalating doses of MM-121 + certain anticancer therapies

Timeline

Start
2011-10
Primary completion
2013-11
Completion
2014-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Cabazitaxel Other / unclassified 20 mg/m2 Intravenous
Subject Cabazitaxel Other / unclassified 25 mg/m2 Intravenous
Subject Gemcitabine Small molecule 1000 mg/m2 Intravenous
Subject Gemcitabine Small molecule 1250 mg/m2 Intravenous
Subject Seribantumab Monoclonal antibody 12 mg/kg Intravenous
Subject Seribantumab Monoclonal antibody 20 mg/kg Intravenous
Background Carboplatin Small molecule 6 unknown
Background Pemetrexed Small molecule 500 mg/m2 Intravenous

Indications