Sanofi wins US approval for multiple myeloma drug in newly …
WEB2 days ago · Sept 20 - The U.S. Food and Drug Administration said on Friday it has approved the use of a drug combination along with Sanofi's (SASY.PA) Sarclisa infusion as a treatment for certain types of ...
FDA Approves Sarclisa with VRd | Int'l Myeloma Foundation
WEB3 days ago · According to a September 20, 2024, press release, the U.S. Food and Drug Administration (FDA) has "approved isatuximab-irfc (Sarclisa, Sanofi-Aventis U.S. LLC) with bortezomib, lenalidomide, and dexamethasone for adults with newly diagnosed multiple myeloma who are not eligible for autologous stem cell transplant (ASCT)." This approval was based on results of the phase III IMROZ clinical trial ...
Advances in multiple myeloma treatment - Mayo Clinic …
WEBMay 16, 2024 · Right now, there is no cure for the disease. But as Dr. Joselle Cook, a Mayo Clinic hematologist, explains, recent advances in treatment are helping people live longer. And as multiple myeloma research continues, a cure may someday be on the horizon.
FDA approves isatuximab-irfc with bortezomib, lenalidomide, and ...
WEB3 days ago · Efficacy was evaluated in IMROZ (NCT03319667), an open-label, randomized, active-controlled phase 3 trial in patients with newly diagnosed multiple myeloma who were not eligible for ASCT.
Multiple Myeloma: Improved Prognosis With the Latest Treatments
WEBAug 16, 2023 · The overall five-year survival rate for people with active multiple myeloma in the United States has increased steadily over time, to more than 55% today. It’s important to remember that even the most recent statistics apply to many people who did not have access to the newer treatments.
Daratumumab Plus Standard Therapy for Multiple Myeloma
WEBJan 19, 2024 · A large randomized clinical trial for people newly diagnosed with multiple myeloma has found that adding the drug daratumumab (Darzalex) to a standard treatment regimen was more effective than that standard regimen on its own.
FDA’s Recent Approval of 2 CAR T-Cell Therapies a ‘Big Step …
WEBRye Brook, N.Y., April 16, 2024 – The U.S. Food and Drug Administration (FDA) recently approved the CAR T-cell therapies ciltacabtagene autoleucel (cilta-cel; Carvykti™) and idecabtagene vicleucel (ide-cel; Abecma®) for earlier …
FDA Approves Carvykti CAR T-Cell Therapy for Multiple Myeloma
WEBMar 30, 2022 · On February 28, the Food and Drug Administration (FDA) approved ciltacabtagene autoleucel (Carvykti) for adults with multiple myeloma that is not responding to treatment (refractory) or has returned after treatment (relapsed).
CAR T-Cell Therapy Approved for Multiple Myeloma - NCI
WEBApr 14, 2021 · A type of immunotherapy called CAR T-cell therapy is now an option for some people with multiple myeloma. On March 26, the Food and Drug Administration (FDA) approved idecabtagene vicleucel (Abecma) for people with multiple myeloma that has not responded to or has returned after at least four different prior cancer treatments.
FDA Approves First Cell-Based Gene Therapy for Adult Patients …
WEBMarch 27, 2021. The U.S. Food and Drug Administration approved Abecma (idecabtagene vicleucel), a cell-based gene therapy to treat adult patients with multiple myeloma who have not responded...