
FDA Approves Sarclisa In Newly Diagnosed Transplant-Ineligible Multiple Myeloma
The Food and Drug Administration has approved Sarclisa as a first-line treatment for patients with multiple myeloma who are ineligible for autologous stem cell transplant.
The Food and Drug Administration (FDA) has approved Sarclisa (isatuximab-irfc) with Velcade (bortezomib), Revlimid (lenalidomide) and dexamethasone,
The efficacy of Sarclisa, the FDA announced, was determined in the IMROX phase 3 trial, which enrolled 446 patients to receive the Velcade, Revlimid and dexamethasone with or without Sarclisa.
In the trial, the Sarclisa regimen demonstrated a 40% reduction in the risk of disease progression or death. The median progression-free survival (PFS, the time a patient lives without their disease spreading or worsening) was not reached in the Isa-VRd arm, meaning fewer than half of the patients in that arm had experienced disease progression, and 54.3 months in the Sarclisa-free arm.
The most common side effects experienced by at least 20% of participants, the agency reported, were upper respiratory tract infection, diarrhea, fatigue, peripheral sensory neuropathy, pneumonia, musculoskeletal pain, cataract, constipation, peripheral edema, rash, infusion-related reaction, insomnia and COVID-19 infection.
According to the National Cancer Institute, Sarclisa is a monoclonal antibody that binds to the protein CD38 found on some immune and cancer cells, including myeloma cells, and may block CD38 and help the immune system kill cancer cells.
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