Ichnos Glenmark Innovation presents first clinical data from phase 1 study of Trispecific TREAT Antibody, ISB 2001
Express Pharma
DECEMBER 9, 2024
ISB2001 Phase 1 Dose Escalation Study Design The Phase 1, first-in-human, open-label study is evaluating the safety and anti-myeloma activity of ISB2001 in patients with RRMM. No immune cell-associated neurotoxicity syndrome (ICANS) was observed. The median duration of CRS was 2 days (range: 18).
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