The European Commission has granted conditional marketing authorization (Aic) for idecabtagene vicleucel (Ide-cel), the first T-cell based immunotherapy with chimeric antigen receptor (Car-T) directed against maturation antigen B cell (Bcma), for the treatment of adult patients with relapsed and refractory multiple myeloma who have received at least 3 prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti-CD38 antibody, and who have demonstrated disease progression to the last therapy. This was announced by Bristol Myers Squibb (Bms), noting that Ide-cel is the first and only approved Car-T therapy aimed at recognizing and binding to Bcma, a protein almost universally expressed on multiple myeloma cells, killing diseased cells.
Read Also
- United for a #SpecialityUrgenciasYA | Health News May 27, 2021
- Covid vaccine, Galli: “Third dose does not convince me” Aug 17, 2021
- National tourism is out of control and exceeds prepandemic levels in July Aug 24, 2021
- What we know about “black fungus” in India May 27, 2021
- Help for the elderly : France, the lack of arms Jun 25, 2020
- These products are able to accelerate a metabolism Jul 9, 2020
- Dr. Quiñones-Hinojosa: We understand less than 1% of the brain May 27, 2021
