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Cellectis Receives Orphan Drug Designation for UCART22, its Allogeneic CAR T Product for Patients with Acute Lymphoblastic Leukemia

Cellectis Receives Orphan Drug Designation for UCART22, its Allogeneic CAR T Product for Patients with Acute Lymphoblastic Leukemia
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Cellectis Receives Orphan Drug Designation for UCART22, its Allogeneic CAR T Product for ...

NEW YORK, June 04, 2024 (GLOBE NEWSWIRE) Cellectis (the “Company”) (Euronext Growth: ALCLS - NASDAQ: CLLS), a clinical-stage biotechnology company using its pioneering gene-editing platform to develop life-saving cell ....

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Immix Biopharma Awarded European Union Orphan Drug Designation for NXC-201 in Multiple Myeloma

European Orphan Drug Designation qualifies NXC-201 for: 10 years of market exclusivity once authorized in the EUAccess to the EU centralized authorization procedureReduced fees for: EU protocol. ....

Gabriel-morris , Mike-moyer , Ilya-rachman , European-commission , Exchange-commission , Company-annual-report-on-form , European-medicines-agency , European-union , Nasdaq , Committee-for-orphan-medicinal-products , Immix-biopharma-inc , Company-contact

Immix Biopharma Awarded European Union Orphan Drug Designation for NXC-201 in AL Amyloidosis

European Orphan Drug Designation qualifies NXC-201 for: 10 years of market exclusivity once authorized in the EUAccess to the EU centralized authorization procedureReduced fees for EU protocol. ....

Gabriel-morris , Ilya-rachman , Mike-moyer , Los-angeles , Immix-biopharma-inc , European-commission , European-medicines-agency , Committee-for-orphan-medicinal-products , Nasdaq , Exchange-commission , Company-contact , European-union

Immix Biopharma (IMMX) Granted EU Orphan Drug Designation for NXC-201

Immix Biopharma (IMMX) Granted EU Orphan Drug Designation for NXC-201
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