
Breakthrough for Daratumumab for Use as Second Line With Standard of Care in Multiple Myeloma
The monoclonal antibody daratumumab (Darzalex) has been granted breakthrough designation, the second for this drug, for use in combination with either lenalidomide and dexamethasone or bortezomib and dexamethasone, for patients with multiple myeloma who have received at least 1 prior therapy.
The monoclonal antibody daratumumab (Darzalex) has been granted breakthrough designation, the second for this drug, for use in combination with either lenalidomide (Revlimid) and dexamethasone or bortezomib (Velcade) and dexamethasone, for patients with multiple myeloma who have received at least 1 prior therapy.
The drug was
- MMY3004 (CASTOR) trial, which evaluated daratumumab in combination with the immunomodulatory agent dexamethasone and the proteasomal inhibitor bortezomib, compared with bortezomib and dexamethasone alone, in patients who had received just a single prior line of therapy.
- MMY3003 (POLLUX) trial, which evaluated daratumumab in combination with dexamethasone and the immunomodulatory agent lenalidomide, compared with dexamethasone and lenalidomide alone, in patients who had received just a single prior line of therapy.
Both trials found that including daratumumab reduced the risk of disease progression as well as death in patients with multiple myeloma.
“This is the second time daratumumab has earned the distinction of a Breakthrough Therapy Designation. We are pleased that the FDA continues to recognize the potential of daratumumab to help patients with multiple myeloma. We continue to work with our strategic partner Janssen and the regulatory authorities to advance daratumumab to bring this treatment to more patients suffering from multiple myeloma as quickly as possible,”
Craig L. Tendler, MD, vice president, Late-Stage Development and Global Medical Affairs for Oncology, Hematology and Supportive Care, Janssen,
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