The FDA approves Sanofi’s (SNY +4%) Sarclisa (isatuximab-irfc), combined with Bristol-Myers Squibb’s (BMY +1.7%)
Pomalyst (pomalidomide) and dexamethasone, for adult multiple myeloma
(MM) patients who have received at least two prior lines of therapy,
including lenalidomide (Revlimid) and a proteasome inhibitor. The
agency’s action date was April 30.
Isatuximab is a monoclonal antibody that promotes
programmed tumor cell death via targeting a specific epitope on the CD38
receptor. CD38 is a protein found on the surface of white blood cells.
Related product: Johnson & Johnson’s (JNJ +2.4%) Darzalex (daratumumab), also a C38-directed cytolytic antibody used to treat MM.
https://seekingalpha.com/news/3547590-fda-oks-sanofi-drug-for-previously-treated-multiple-myeloma
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