An Open-Label Treatment Use Protocol for Daratumumab in Subjects with Multiple Myeloma Who Have Received at Least 3 Prior Lines of Therapy (Including a Proteasome Inhibitor and an Immunomodulatory Agent) or are Double Refractory to a Proteasome Inhibitor and an Immunomodulatory Agent
ID Number 15-1307Principal Investigator(s)
Department(s) or Division(s)
Hematology and Medical Oncology
The objective of this study is to provide early access to daratumumab treatment and collect additional safety data. Daratumumab is not approved for use by the U.S. Food and Drug Administration (FDA) or any Regulatory Authority in the European Economic Area (EEA), Eastern Europe, Russia, Asia or any other country.
Recruiting Patients: No