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FDA Grants Breakthrough Therapy Designation to Incyte’s CALR‑Targeting Antibody as ASH Data Show Early Efficacy in Myelofibrosis

Incyte targets a 2026 registrational program in essential thrombocythemia following phase 1 reports of no dose‑limiting toxicities with clinically meaningful spleen and anemia benefits.

Hospital Breathlessness Linked to Sixfold Higher In-Patient Death Risk, Study Finds

FAP-Targeted Radioligand Yields Near-Complete Response in Three Solitary Fibrous Tumor Patients

FDA Approves IL-23 Inhibitor Tremfya for Moderate-to-Severe Crohn’s Disease