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Bristol Myers Squibb (NYSE:BMY) introduced Monday that Reblozyl, an FDA-approved anemia remedy the corporate develops in partnership with Merck (NYSE:MRK), reached the first and key secondary endpoints in a Part 3 trial involving sufferers with myelodysplastic syndromes.
The open-label, randomized examine named COMMANDS was designed to judge Reblozyl versus epoetin alfa, a organic medicine much like human erythropoietin, in sufferers with low/low/intermediate-risk (MDS).
The trial topics had been pink blood cell (RBC) transfusion-dependent and had not beforehand acquired erythropoiesis-stimulating brokers.
An interim evaluation of the examine has indicated that Reblozyl met the first endpoint displaying a “extremely statistically vital and clinically significant enchancment” in RBC transfusion independence with a parallel enhance in hemoglobin as a first-line remedy for adults with MDS.
Bristol Myers (BMY) stated that Reblozyl, also referred to as luspatercept-aamt, demonstrated a security profile in step with findings from one other Part 3 trial referred to as MEDALIST examine.
The corporate plans to conduct an entire evaluation of COMMANDS knowledge for a presentation at an upcoming medical occasion and intends to share the outcomes with well being authorities.
Learn: Wedbush launched its protection on Geron Company (GERN) on Friday with a bullish view evaluating its experimental MDS remedy imetelstat with Reblozyl.
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