Ichnos Glenmark Innovation (IGI) erhält FDA-Fast-Track-Zulassung für ISB 2001 zur Behandlung des rezidivierten/refraktären multiplen Myeloms ...Middle East

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Ergebnisse des Dosis-Eskalationsteils der klinischen Phase-1-Studie mit ISB 2001 bei Patienten mit stark vorbehandeltem multiplem Myelom werden auf der ASCO-Jahrestagung 2025 vorgestellt NEW YORK, 6. Mai 2025 /PRNewswire/ -- IGI, ein globales, voll integriertes Biotechnologieunternehmen...

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