Highlights

07/03 Incyte Corporation Receives Complete Response Letter From FDA For Zynyz Supplemental Biologics License Application CI
07/03 Incyte announces the European Commission approval of Zynyz® (retifanlimab) for the first-line treatment of advanced squamous cell carcinoma of the anal canal (SCAC) RE
07/03 Incyte Announces European Commission Approval of Zynyz (Retifanlimab) for First-Line Treatment of Advanced Squamous Cell Carcinoma of the Anal Canal CI
28/02 Sector Update: Health Care Stocks Advance Late Afternoon MT
27/02 Eli Lilly and Company's Olumiant Recommends by CHMP for Approval of Expanded Use in the European Union for Adolescents with Severe Alopecia Areata CI
27/02 Eli Lilly, Incyte Say They Get EMA Panel's Positive Opinion for Olumiant to Treat Severe Alopecia Areata MT
18/02 United Medical Ltda Announces Regulatory Submission of NIKTIMVO in Brazil CI
14/02 Incyte's weak Opzelura 2026 revenue forecast heightens Jakafi patent concerns (Feb 10) RE
10/02 Incyte Corporation Reports Earnings Results for the Fourth Quarter and Full Year Ended December 31, 2025 CI
10/02 Incyte Q4 Adjusted Earnings, Revenue Rise; Shares Down Pre-Bell MT
10/02 Incyte Corporation Provides Earnings Guidance for the Fiscal Year 2026 CI
10/02 Earnings Flash (INCY) Incyte Corporation Reports Q4 Revenue $1.51B, vs. FactSet Est of $1.35B MT
10/02 Earnings Flash (INCY) Incyte Corporation Posts Q4 Adjusted EPS $1.80 per Share, vs. FactSet Est of $2.44 MT
06/02 Diary - U.S. earnings week ahead RE
03/02 Prelude Therapeutics Incorporated Receives FDA Clearance of Investigational New Drug Application for PRT12396 CI
30/01 Incyte Announces Positive CHMP Opinion for Zynyz®? (retifanlimab) for First-Line Treatment of Advanced Squamous Cell Carcinoma of the Anal Canal CI
05/01 Incyte Announces Positive Topline Results from Pivotal Study of Tafasitamab (Monjuvi/Minjuvi) as First-Line Treatment for Diffuse Large B-Cell Lymphoma CI
05/01 Incyte announces positive topline results from study of tafasitamab RE
22/12 Incyte Says Its Cancer Drug Has Received Approval in Japan for Follicular Lymphoma MT
18/12 Incyte announces European Commission approval of Minjuvi (tafasitamab) RE
17/12 Incyte Announces European Commission Approval of Minjuvi (Tafasitamab) for the Treatment of Relapsed or Refractory Follicular Lymphoma CI
17/12 Incyte Says European Commission Approves Minjuvi Combination Therapy for Follicular Lymphoma MT
08/12 Incyte Says Rare Blood Cancer Therapy Receives FDA Breakthrough Designation MT
07/12 Incyte Announces New Positive Data for INCA033989, Its First-In-Class mutCALR-Targeted Monoclonal Antibody, in Patients with Myelofibrosis Presented At ASH 2025 CI
07/12 Incyte's First-In-Class mutCALR-Targeted Monoclonal Antibody, INCA033989, Granted Breakthrough Therapy Designation by U.S. FDA CI
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