drugset / Trial / NCT02326025

A Study of Olaratumab and Doxorubicin in Participants With Advanced Soft Tissue Sarcoma

NCT02326025

Phase 1 Completed 49 enrolled Eli Lilly and Company
Non-randomizedSequentialOpen-labelBasic science

Summary

The purpose of this study is to assess how the body handles olaratumab when it is given with another drug called doxorubicin. The safety and tolerability of these drugs will be studied. Each participant will complete two 21-day cycles in a fixed order. Participants who complete Cycle 2 may continue to receive olaratumab + doxorubicin for an additional six 21-day cycles and then may receive olaratumab alone until discontinuation criteria are met. Screening is required within 21 days prior to first dose. Part B was added in October, 2015 to assess how the body handles a higher dose of olaratumab when given with doxorubicin. Participants may only enroll in one part.

Timeline

Start
2015-01-22
Primary completion
2015-05-20
Completion
2018-11-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Doxorubicin Other / unclassified 75 mg/m2 Intravenous
Subject Olaratumab Monoclonal antibody 15 mg/kg Intravenous
Subject Olaratumab Monoclonal antibody 20 mg/kg Intravenous

Indications