Bristol-Myers
Squibb Company BMY and AbbVie ABBV today announced updated efficacy and safety data from a small,
randomized Phase 2, open-label study in patients with previously-treated
multiple myeloma that evaluated two doses of the investigational
monoclonal antibody elotuzumab (10 mg/kg and 20 mg/kg) in combination
with lenalidomide and low-dose dexamethasone. In the 10 mg/kg arm
(N=36), which is the dose used in the ongoing Phase 3 trials, median
progression-free survival (PFS), or the time without disease
progression, was 33 months after a median follow-up of 20.8 months (95%
CI: 14.9-NA) and the objective response rate (ORR) was 92%. As
previously reported, median PFS was 18 months in the 20 mg/kg arm (N=37)
after a median follow-up
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