U.S. FDA Approves CARVYKTI (ciltacabtagene autoleucel), Janssen's First Cell Therapy, a BCMA-Directed CAR-T Immunotherapy for the Treatment of Patients with Relapsed or Refractory Multiple Myeloma'

Press/Media

Period28 Feb 2022

Media coverage

1

Media coverage

  • TitleU.S. FDA Approves CARVYKTI (ciltacabtagene autoleucel), Janssen's First Cell Therapy, a BCMA-Directed CAR-T Immunotherapy for the Treatment of Patients with Relapsed or Refractory Multiple Myeloma'
    Media name/outletMENAFN -Press Releases (English)
    Country/TerritoryJordan
    Date28/02/22
    PersonsSundar Jagannath