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US45337C1027

Produits pharmaceutiques

Temps réel estimé Cboe BZX Autres places de cotation 17:55:35 29/07/2026			Varia. 5j.	Varia. 1 janv.
126,95 ^USD	-2,29%		+9,20%	+28,01%

17:30	INCYTE CORPORATION : RBC Capital Markets maintient sa recommandation neutre	ZM
17:27	INCYTE CORPORATION : Goldman Sachs confirme sa recommandation neutre	ZM

Communiqués

12:02	Opzelura® (ruxolitinib) Cream Becomes First Steroid-Free Topical JAK Inhibitor Approved in the European Union for Adults with Moderate Atopic Dermatitis	BU
28/07	Incyte: Q2 Earnings Snapshot	AQ
28/07	Incyte Reports Second Quarter 2026 Financial Results and Provides Business Updates	BU
18/07	Les données d'Incyte seront présentées durant quatre présentations orales rapides au Congrès 2026 de la Société européenne d'oncologie médicale (ESMO) pour soutenir les efforts visant à améliorer les résultats dans les cancers difficiles à traiter	BU
17/07	Incyte Data to Be Highlighted in Four Rapid Oral Presentations at the European Society for Medical Oncology (ESMO) Congress 2026 Support Efforts to Improve Outcomes in Difficult-to-Treat Cancers	BU
14/07	Incyte présente les données de phase 1/2 sur les doses multiples du VGA039 (latarcibart) lors du congrès de l’ISTH 2026, montrant une réduction significative des hémorragies chez les patients atteints de tous les types de maladie de von Willebrand	BU
13/07	Incyte Presents Phase 1/2 Multidose Data for VGA039 (Latarcibart) at ISTH 2026, Showing Substantial Bleed Reductions in Patients with all Von Willebrand Disease Types	BU
08/07	Incyte to Report Second Quarter Financial Results	BU
06/07	Incyte Completes Acquisition of Vega Therapeutics, a Wholly Owned Subsidiary of Star Therapeutics, Expanding its Hematology Portfolio	BU
27/06	Incyte annonce un avis favorable du CHMP concernant la crème Opzelura® (ruxolitinib) pour le traitement des adultes atteints de dermatite atopique modérée	BU
26/06	Incyte Announces Positive CHMP Opinion for Opzelura® (ruxolitinib) Cream for the Treatment of Adults with Moderate Atopic Dermatitis	BU
24/06	Both Sides Receive Skepticism From Ninth Circuit In SEC v. Panuwat Oral Argument	AQ
19/06	Incyte Japan annonce l’autorisation de mise sur le marché de Minjuvi® (tafasitamab) en association avec la lénalidomide pour le traitement des adultes atteints d’un lymphome diffus à grandes cellules B (LDGCB) récidivant ou réfractaire	BU
19/06	Incyte Japan Announces Approval of Minjuvi® (tafasitamab) in Combination with Lenalidomide for the Treatment of Adults with Relapsed or Refractory Diffuse Large B-Cell Lymphoma (DLBCL)	BU
15/06	Incyte annonce de nouvelles données positives à l'EHA 2026 qui indiquent qu'INCA033989 a obtenu des réponses cliniques et moléculaires rapides, robustes et soutenues et a été bien toléré chez les patients atteints de myélofibrose...	BU
15/06	Les résultats de l’essai pivot de phase 3 frontMIND mené par Incyte sur l’association thérapeutique à base de tafasitamab (Monjuvi®/Minjuvi®), présentés lors de la séance plénière du congrès 2026 de l’Association européenne d’hématologie (EHA)...	BU
14/06	Incyte : Mirum Pharmaceuticals and Incyte Announce Positive Pivotal Phase 2 Results from PROGRESS Study of Zilurgisertib in Fibrodysplasia Ossificans Progressiva	PU
13/06	Incyte Announces New Positive Data at EHA 2026 Showed INCA033989 Achieved Rapid, Robust and Sustained Clinical and Molecular Responses and Was Well Tolerated in Patients with Myelofibrosis and Essential Thrombocythemia	BU
13/06	Results from Incyte’s Pivotal Phase 3 frontMIND Trial of Tafasitamab (Monjuvi®/Minjuvi®) Combination Presented at the 2026 European Hematology Association (EHA) Congress Plenary Showed Prolonged Progression Free Survival	BU
08/06	Incyte to Acquire Vega Therapeutics, a Wholly Owned Subsidiary of Star Therapeutics, Expanding its Hematology Portfolio into Bleeding Disorders	BU
30/05	L’essai pivot frontMIND d’Incyte a montré que l’association à base de tafasitamab (Monjuvi®/Minjuvi®) prolongeait significativement la survie sans progression, réduisant de 25 % le risque de progression de la maladie ou de décès chez les patients...	BU
30/05	Incyte’s Pivotal frontMIND Trial Showed Tafasitamab (Monjuvi®/Minjuvi®) Combination Significantly Prolonged Progression-free Survival, Reducing the Risk of Disease Progression or Death by 25% in Patients with Previously Untreated, High-risk DLBCL	BU
26/05	Incyte to Present at the Goldman Sachs 47th Annual Global Healthcare Conference	BU
20/05	Incyte and Genesis Expand Molecular AI Collaboration to Accelerate Drug Discovery	BU
19/05	Incyte and Edison Scientific Announce Strategic Collaboration to Employ the Kosmos AI Platform for Research and Development	BU