CASI Pharmaceuticals Reports 80% Efficacy in Phase 1 Study of CID-103 for Immune Thrombocytopenia

Reuters
01/12
CASI Pharmaceuticals Reports 80% Efficacy in Phase 1 Study of CID-103 for Immune Thrombocytopenia

CASI Pharmaceuticals Inc. announced updated results from its Phase 1 open-label study of CID-103, an anti-CD38 monoclonal antibody, in adult patients with immune thrombocytopenia $(ITP)$. The company reported that 80% of patients achieved the primary efficacy endpoint and noted favorable safety and tolerability findings. Initial clinical data from this study were presented at the 67th American Society of Hematology Annual Meeting and Exposition in December 2025, with additional proof of concept data now available. CASI Pharmaceuticals stated that further updates from the study will be provided as it progresses.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. CASI Pharmaceuticals Inc. published the original content used to generate this news brief via ACCESS Newswire (Ref. ID: 1126262) on January 12, 2026, and is solely responsible for the information contained therein.

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