Access to Belantamab Mafodotin for People with Multiple Myeloma

Full Title

Expanded Access Program for Belantamab Mafodotin in combination with either bortezomib/dexamethasone or pomalidomide/dexamethasone in patients with multiple myeloma previously treated with at least one prior line of therapy Study title for participants: Managed Access Program for combination treatment with belantamab mafodotin in multiple myeloma

Purpose

This study offers access to the investigational drug belantamab mafodotin for people with multiple myeloma that has come back or continued to grow despite treatment. It is available for patients who previously received it and benefited from it as well as people with persistent multiple myeloma who have not yet received it.

Belantamab mafodotin is made up of an antibody and a chemotherapy drug. The antibody binds to the BCMA protein on multiple myeloma cells, and the chemotherapy enters the cells to kill them. The medication is given intravenously (by vein). Because belantamab mafodotin can cause eye problems as a side effect, participants in this study will also have an eye exam and be monitored for eye problems.

Who Can Join

To be eligible for this study, patients must meet several requirements, including:

• This study is open to patients who previously received belantamab mafodotin and benefited from it as well as people with persistent multiple myeloma who have not yet received it.
• Patients who have not yet received belantamab mafodotin must have multiple myeloma that persists despite at least four prior regimens of treatment.
• This study is for people age 18 and older.

Contact

For more information and to ask about eligibility for this study, please contact the office of Dr. Malin Hultcrantz at 646-608-3714.