FDA Grants Orphan Drug and Rare Pediatric Disease Designation Status to Cellectis’ UCART22 product candidate for Acute Lymphoblastic Leukemia (ALL) Treatment. Full press release available here: https://lnkd.in/g6Y5pNnE #allogeneic, #celltherapy, #genetherapy
Bonne nouvelle !
Congratulations to the Cellectis team !
Bonne nouvelle !
Congrats to the Cellectis Team!
What an achievement !
Congratulations Andre Choulika Ph.D. !
Great News!
Head of Legal and Compliance and DPO - Responsable juridique et Compliance et DPO chez HTL Biotechnology
2moCongratulations, Cellectis !