drugset / Trial / NCT00747123

A Safety, Tolerability and Efficacy Study of ACE-011 in Patients With Osteolytic Lesions of Multiple Myeloma

NCT00747123

Phase 2 Completed 30 enrolled Celgene Corporation
RandomizedParallel-groupDouble-blindTreatment

Summary

Multi-center, randomized, multiple-dose study to evaluate the safety, tolerability and efficacy of ACE-011 in patients with osteolytic lesions of multiple myeloma.

Timeline

Start
2008-09-01
Primary completion
2009-08-01
Completion
2009-08-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Sotatercept Protein / enzyme biologic 0.1 mg/kg Subcutaneous
Subject Sotatercept Protein / enzyme biologic 0.3 mg/kg Subcutaneous
Subject Sotatercept Protein / enzyme biologic 0.5 mg/kg Subcutaneous

Indications