Bristol-Myers Empliciti Combo Fails In First-Line Myeloma Study

 | Mar 09, 2020 09:50PM ET

Bristol-Myers Squibb Company (NYSE:BMY) announced that a phase III ELOQUENT-1 study evaluating Empliciti (elotuzumab) triplet combination in first-line patients with multiple myeloma, who are transplant ineligible, failed to meet its primary endpoint.

The ELOQUENT-1 study compared Empliciti in combination with Revlimid plus dexamethasone (ERd) to a combination of Revlimid and dexamethasone (Rd) in newly diagnosed, previously untreated multiple myeloma patients, who are ineligible for a transplant, for improvement in progression-free survival ("PFS"). Data from the study showed that the ERd combo failed to demonstrate statistically significant improvement in PFS. However, safety profile of the Empliciti triplet combination was consistent with previous clinical studies.

Detailed data from the study will be presented at a future medical meeting.

Please note that ERd combo is already approved for the treatment of relapsed and refractory multiple myeloma (r/rMM) in second or later-line settings. The treatment regimen is also the standard of care in its approved indication. Empliciti is also approved in combination with Pomalyst plus dexamethasone for treating multiple myeloma patients, who have received at least two prior therapies, including lenalidomide and a proteasome inhibitor. Bristol-Myers co-develops Empliciti in collaboration with AbbVie (NYSE:ABBV) . Bristol-Myers is solely responsible for the drug’s commercialization activities.

Shares of Bristol-Myers have increased 13.3% in the past year against the industry ’s decrease of 0.8%.