I1NC34 Aperçu des actions Incyte Corporation, société biopharmaceutique, se consacre à la découverte, au développement et à la commercialisation de produits thérapeutiques dans les domaines de l'hématologie/oncologie, de l'inflammation et de l'auto-immunité aux États-Unis et dans le monde entier. Plus de détails
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Incyte Corporation Concurrents Historique des prix et performances
Résumé des hausses, des baisses et des variations du cours de l'action pour la période du 1er janvier au 31 décembre 2009 Incyte Historique des cours de bourse Prix actuel de l'action US$221.76 Plus haut sur 52 semaines US$232.20 Plus bas sur 52 semaines US$135.90 Bêta 0.70 Variation sur 1 mois -4.50% Variation sur 3 mois 25.57% Variation sur 1 an 45.28% Variation sur 3 ans 4.64% Variation sur 5 ans n/a Évolution depuis l'introduction en bourse 38.34%
Nouvelles et mises à jour récentes
Incyte Announces Positive Results from Phase 3 Trial Evaluating Retifanlimab in Combination with Platinum-Based Chemotherapy in Patients with Non-Small Cell Lung Cancer Dec 08
Incyte Provides Update on Early Phase MRGPRX2 and MRGPRX4 Programs Nov 19
Incyte Corporation to Report Q3, 2024 Results on Oct 29, 2024 Oct 08 Incyte 's Cdk2 Inhibitor Incb123667 Shows Promising Evidence of Clinical Activity in Patients with Advanced Solid Tumors, Notably Ovarian Cancer
Incyte Announces Positive Topline Results from Pivotal Study of Tafasitamab (Monjuvi®) in Relapsed or Refractory Follicular Lymphoma Aug 16
Incyte and Syndax Pharmaceuticals Announce U.S. FDA Approval of Niktimvo™ (axatilimab-csfr) for the Treatment of Chronic Graft-Versus-Host Disease (GVHD) Aug 15 Voir plus de mises à jour
Incyte Announces Positive Results from Phase 3 Trial Evaluating Retifanlimab in Combination with Platinum-Based Chemotherapy in Patients with Non-Small Cell Lung Cancer Dec 08
Incyte Provides Update on Early Phase MRGPRX2 and MRGPRX4 Programs Nov 19
Incyte Corporation to Report Q3, 2024 Results on Oct 29, 2024 Oct 08 Incyte 's Cdk2 Inhibitor Incb123667 Shows Promising Evidence of Clinical Activity in Patients with Advanced Solid Tumors, Notably Ovarian Cancer
Incyte Announces Positive Topline Results from Pivotal Study of Tafasitamab (Monjuvi®) in Relapsed or Refractory Follicular Lymphoma Aug 16
Incyte and Syndax Pharmaceuticals Announce U.S. FDA Approval of Niktimvo™ (axatilimab-csfr) for the Treatment of Chronic Graft-Versus-Host Disease (GVHD) Aug 15
Incyte Corporation to Report Q2, 2024 Results on Jul 30, 2024 Jul 10
Incyte Corporation (NasdaqGS:INCY) acquired Escient Pharmaceuticals, Inc. from a group of shareholders. Jun 01 Incyte Corporation (NasdaqGS:INCY) announces an Equity Buyback for $1,672 million worth of its shares. May 16
Incyte Corporation (NasdaqGS:INCY) announces an Equity Buyback for $1,672 million worth of its shares. May 14
Incyte Corporation, Annual General Meeting, Jun 12, 2024 May 01
Incyte Corporation Maintains Earnings Guidance for 2024 Apr 30
Incyte Corporation (NasdaqGS:INCY) entered into a definitive agreement to acquire Escient Pharmaceuticals, Inc. from a group of shareholders for $750 million. Apr 23
Incyte Corporation to Report Q1, 2024 Results on Apr 30, 2024 Apr 12
Incyte Announces New Results from A Phase 2 Study Evaluating the Efficacy and Safety of Twice-Daily Ruxolitinib Cream 1.5% (Opzelura®) in Adult Patients with Hurley Stage 1 or 2 (Mild-To-Moderate) Hidradenitis Suppurativa (HS) Mar 11
Incyte Corporation Provides Earnings Guidance for 2024 Feb 14
Incyte Corporation to Report Q4, 2023 Results on Feb 13, 2024 Jan 24
Incyte and Syndax Pharmaceuticals Present Additional Data from Positive AGAVE-201 Trial at ASH Plenary Session Showing Axatilimab Efficacy Including Durable Responses in Chronic Graft-Versus-Host Disease Dec 11
Incyte Corporation Provides Earning Guidance for the Full Year 2023 Nov 01 Incyte Announces New Data for Ruxolitinib Cream (Opzelura®) in Children with Atopic Dermatitis
Incyte Announces Positive 52-Week Data from Phase 2b Study Evaluating Povorcitinib (INCB54707) in Patients with Extensive Nonsegmental Vitiligo Oct 12
Incyte Corporation to Report Q3, 2023 Results on Oct 31, 2023 Oct 11
Incyte Corporation Announces Executive Changes, Effective November 1, 2023 Sep 14
Incyte Corporation Revises Earnings Guidance for the Year 2023 Aug 02
Syndax Pharmaceuticals and Incyte Announce Positive Topline Results from the Pivotal Agave-201 Trial of Axatilimab in Chronic Graft-Versus-Host Disease Jul 25 Incyte Corporation to Report Q2, 2023 Final Results on Aug 01, 2023
Incyte Corporation Appoints Pablo J. Cagnoni, M.D. as President and Head of Research & Development, Effective June 5, 2023 May 09
Incyte Announces 52-Week Results from Phase 2 Study Evaluating Povorcitinib (INCB54707) in Patients with Hidradenitis Suppurativa Feb 11 Incyte Corporation Provides Earnings Guidance for the Year 2023
Incyte Corporation to Report Q4, 2022 Results on Feb 07, 2023 Jan 18
Incyte Announces Data from Two LIMBER Studies Evaluating Combination Treatments in Patients with Myelofibrosis Dec 13
Syndax Pharmaceuticals and Incyte Announce Axatilimab Phase 1/2 Data in Patients with Chronic Graft-Versus-Host Disease Published in the Journal of Clinical Oncology Dec 06
Incyte Corporation Announces Pivotal Phase 3 Data Showing Significant Improvements in Facial and Total Body Repigmentation with Ruxolitinib Cream (Opzelura™) in Vitiligo Published in New England Journal of Medicine Oct 20
Incyte Corporation to Report Q3, 2022 Results on Nov 01, 2022 Oct 12
Incyte Announces the Appointment of Susanne Schaffert as New Member of Its Board of Directors Oct 05
Incyte Corporation (NasdaqGS:INCY) entered into an agreement to acquire Villaris Therapeutics, Inc. from Medicxi Ventures (UK) LLP and others for $1.4 billion. Oct 04
Incyte Corporation Announces FDA Approval Of Pemazyre® (Pemigatinib) As The First And Only Targeted Treatment For Myeloid/Lymphoid Neoplasms (MLNs) With FGFR1 Rearrangement Aug 27
Incyte Corporation Reaffirms Revenue Guidance for the Full Year 2022 Aug 03
Incyte Corporation Announces U.S. FDA Approval of Opzelura Cream for the Treatment of Vitiligo Jul 19
Incyte Corporation to Report Q2, 2022 Results on Aug 02, 2022 Jul 13
FDA Approves Eli Lilly and Company and Incyte's OLUMIANT® (baricitinib) as First and Only Systemic Medicine for Adults with Severe Alopecia Areata Jun 14
Chmp Recommends Approval of Eli Lilly and Company and Incyte's Olumiant® (Baricitinib) as the First and Only Centrally-Authorized Treatment for Adults with Severe Alopecia Areata (Aa) May 21
FDA Approves Lilly and Incyte's OLUMIANT® (baricitinib) for the Treatment of Certain Hospitalized Patients with COVID-19 May 12
Incyte Announces European Commission Approval of Jakavi (Ruxolitinib) as the First Post-Steroid Treatment for Acute and Chronic Graft-Versus-Host Disease May 05
Incyte Corporation, Annual General Meeting, Jun 15, 2022 May 02
Incyte Announces Positive Committee for Medicinal Products Opinion for Capmatinib (Tabrecta®) for the Treatment of Metex14 Advanced Non-Small Cell Lung Cancer Apr 23
Incyte Corporation to Report Q1, 2022 Results on May 03, 2022 Apr 13
Incyte Corporation Provides Revenue Guidance for the Full Year 2022 Feb 09
Incyte Announces Acceptance and Priority Review of SNDA for Ruxolitinib Cream (Opzelura) as a Treatment for Patients with Vitiligo Dec 15 MorphoSys and Incyte Announce Additional Real-World Evidence Results from RE-MIND2 Study of Tafasitamab (Monjuvi®) in Combination with Lenalidomide for the Treatment of Relapsed or Refractory Diffuse Large B-Cell Lymphoma
Incyte Corporation (NasdaqGS:INCY) entered into stock purchase agreement to acquire 2.92% Syndax Pharmaceuticals, Inc. (NasdaqGS : SNDX) for $35 million. Sep 29 Incyte Announces FDA Approval of Jakafi® (ruxolitinib) for Treatment of Chronic Graft-Versus-Host Disease (GVHD)
Incyte Announces U.S. FDA Approval of Opzelura™ (ruxolitinib) Cream, a Topical JAK Inhibitor, for the Treatment of Atopic Dermatitis (AD) Sep 23
Incyte Announces Health Canada Conditional Approval of Pemazyre® (pemigatinib) as First Targeted Treatment for Adults Sep 20
Calithera Biosciences, Inc. Enters into A Settlement Agreement and Release with Incyte Corporation Sep 19
Incyte Announces Health Canada Approval of Minjuvi® in Combination with Lenalidomide for the Treatment of Adults with Relapsed or Refractory Diffuse Large B-Cell Lymphoma Aug 25
Eli Lilly and Company and Incyte Announce Results from an Additional Cohort of 101 Adult Patients from the COV-Barrier Trial Aug 05
Incyte Announces Positive Phase 3 REACH3 Study Data Published in NEJM for Ruxolitinib (Jakafi) in Chronic Graft-Versus-Host Disease Jul 15
Incyte and MorphoSys Announce Positive CHMP Opinion for Tafasitamab in Combination with Lenalidomide for the Treatment of Adults with Relapsed or Refractory Diffuse Large B-Cell Lymphoma Jun 26
Incyte Announces U.S. FDA Has Extended the New Drug Application Review Period for Ruxolitinib Cream for the Treatment of Atopic Dermatitis Jun 12
Incyte Corporation Announces U.S. Food and Drug Administration Extends sNDA Review Period for Ruxolitinib (Jakafi®) in Chronic Graft-Versus-Host Disease Jun 09
Incyte and MorphoSys US, Inc. Announce Three-Year Results from Phase 2 L-MIND Study of Tafasitamab in Combination with Lenalidomide for the Treatment of Relapsed or Refractory DLBCL Jun 05
Incyte Corporation Announces Positive Primary Analysis from the Phase 2 Optic Study of Ponatinib (Iclusig®) in Chronic Phase-Chronic Myeloid Leukemia (Cp-Cml) to Be Presented At the 2021 Asco Annual Meeting May 21
Incyte Announces Positive Results from Phase 3 TRuE-V Program Evaluating Ruxolitinib Cream in Patients with Vitiligo May 18
Incyte and MorphoSys Announce First Patient Dosed in Phase 3 frontMIND Study Evaluating Tafasitamab Combination as a First-Line Treatment for Diffuse Large B-Cell Lymphoma May 12
Incyte Corporation Provides Revenue Guidance for the Full Year 2021 May 05
Incyte Announces Results from the Phase 3 DEVENT Study Evaluating Ruxolitinib (Jakafi®) as a Treatment for Patients with COVID-19 Associated Acute Respiratory Distress Syndrome (ARDS) on Mechanical Ventilation Mar 19
Eli Lilly and Company and Incyte Announce Top-Line Results from BRAVE-AA2 Mar 04
Incyte Announces the Validation by the European Medicines Agency of Its Marketing Authorization Application for Retifanlimab as Treatment for Patients with Squamous Cell Anal Carcinoma Feb 26
Incyte Announces Acceptance and Priority Review of sNDA for Jakafi® (Ruxolitinib) as A Treatment for Patients with Chronic Graft-Versus-Host Disease Feb 23
Incyte Announces Acceptance and Priority Review of NDA for Ruxolitinib Cream for Atopic Dermatitis Feb 20
Incyte Announces Positive CHMP Opinion for Pemigatinib for the Treatment of Adults With Previously Treated, Unresectable Locally Advanced or Metastatic Cholangiocarcinoma With a Fibroblast Growth Factor Receptor 2 (FGFR2) Fusion or Rearrangement Jan 31
Incyte Announces Acceptance and Priority Review of BLA for Retifanlimab as A Potential Treatment for Patients with Squamous Cell Carcinoma of the Anal Canal (Scac) Jan 22
Incyte Corporation to Report Q4, 2020 Results on Feb 09, 2021 Jan 20
Incyte Corporation and MorphoSys AG Announce Acceptance by Health Canada of the New Drug Submission for Tafasitamab Jan 13
Morphosys and Incyte Announce the Acceptance of the Swissmedic Marketing Authorization Application for Tafasitamab Jan 06
Incyte and Cellenkos Enter into Global Development Collaboration Agreement for CK0804 Dec 31
Incyte Announces Results of Phase 3 RUXCOVID Study of Ruxolitinib (Jakafi®) as a Treatment for Patients with COVID-19 Associated Cytokine Storm Dec 14 Incyte and MorphoSys AG Announces Data Evaluating Tafasitamab with and Without Lenalidomide in Combination with R-CHOP in Patients with DLBCL Presented At ASH 2020
Incyte Announces Detailed Results from the Pivotal Phase 3 Reach3 Study Dec 06
Eli Lilly and Company and Incyte Announces the U.S. Food and Drug Administration Issued an Emergency Use Authorization for the Distribution and Emergency Use of Baricitinib Nov 20
Xencor, MorphoSys AG and Incyte Enter into Global Development Collaboration for Tafasitamab in Combination with Plamotamab Nov 12
Incyte Corporation Announces Revenues Guidance for the Full Year 2020 Nov 07
Lilly and Incyte Highlight Positive Data for Olumiant® in Rheumatoid Arthritis Nov 05 Eli Lilly and Company and Incyte Corporation Showcase New Data for Baricitinib for the Treatment of Moderate to Severe Atopic Dermatitis
Health Canada Accepts Incyte's New Drug Submission for Pemigatinib as a Treatment for Patients with Cholangiocarcinoma Oct 27
MacroGenics, Inc. Enters into A Commercial Supply Agreement with Incyte Corporation Oct 18
Nimble Therapeutics Inc. Announces Strategic Research Collaboration with Incyte to Discover Novel Peptide-Based Therapeutics Oct 06 Rendement pour les actionnaires I1NC34 BR Biotechs BR Marché 7D 0% -2.9% -3.1% 1Y 45.3% -2.0% -11.4%
Voir le rapport complet des actionnaires
Rendement vs Industrie: I1NC34 a dépassé le secteur BR Biotechs qui a rapporté -2 % au cours de l'année écoulée.
Rendement vs marché: I1NC34 a dépassé le marché BR qui a rapporté -11.4 % au cours de l'année écoulée.
Volatilité des prix Is I1NC34's price volatile compared to industry and market? I1NC34 volatility I1NC34 Average Weekly Movement n/a Biotechs Industry Average Movement 9.1% Market Average Movement 5.1% 10% most volatile stocks in BR Market 9.5% 10% least volatile stocks in BR Market 2.8%
Cours de l'action stable: Le cours de l'action de I1NC34 a été volatil au cours des 3 derniers mois.
Volatilité au fil du temps: Données insuffisantes pour déterminer l'évolution de la volatilité de I1NC34 au cours de l'année écoulée.
À propos de l'entreprise Incyte Corporation, une société biopharmaceutique, se consacre à la découverte, au développement et à la commercialisation de produits thérapeutiques dans les domaines de l'hématologie/oncologie, de l'inflammation et de l'auto-immunité aux États-Unis et dans le monde entier. La société propose JAKAFI (ruxolitinib) pour le traitement de la myélofibrose à risque intermédiaire ou élevé, de la polycythémie vera et de la maladie aiguë du greffon contre l'hôte réfractaire aux stéroïdes ; MONJUVI (tafasitamab-cxix)/MINJUVI (tafasitamab) pour le traitement du lymphome diffus à grandes cellules B récidivant ou réfractaire ; PEMAZYRE (pemigatinib), un inhibiteur de la kinase du récepteur du facteur de croissance des fibroblastes qui agit comme moteur oncogène dans les types de tumeurs liquides et solides ; ICLUSIG (ponatinib) pour traiter la leucémie myéloïde chronique et la leucémie lymphoblastique aiguë à chromosome Philadelphie ; et ZYNYZ (retifanlimab-dlwr) pour traiter les adultes atteints d'un carcinome à cellules de Merkel métastatique ou récurrent localement avancé, ainsi que la crème OPZELURA pour le traitement de la dermatite atopique. Ses produits en phase clinique comprennent le retifanlimab, qui fait l'objet d'essais cliniques de phase 3 pour le carcinome épidermoïde du canal anal et le cancer du poumon non à petites cellules ; l'axatilimab, un anticorps monoclonal anti-CSF-1R en phase 2, qui est développé comme traitement pour les patients atteints de GVHD chronique ; l'INCA033989 pour inhiber l'oncogenèse ; l'INCB160058, qui est développé comme traitement de fond ; et l'INCB99280 et l'INCB99318 pour le traitement des tumeurs solides.
Afficher plus Incyte Corporation Résumé des fondamentaux Comment les bénéfices et les revenus de Incyte se comparent-ils à sa capitalisation boursière ? I1NC34 statistiques fondamentales Capitalisation boursière R$79.39b Bénéfices(TTM) R$199.61m Recettes(TTM ) R$25.05b
Bénéfices et recettes Principales statistiques de rentabilité tirées du dernier rapport sur les bénéfices (TTM) I1NC34 compte de résultat (TTM ) Recettes US$4.08b Coût des recettes US$2.88b Marge brute US$1.20b Autres dépenses US$1.16b Les revenus US$32.48m
Derniers bénéfices déclarés
Sep 30, 2024
Prochaine date de publication des résultats
s/o
Résultat par action (EPS) 0.17 Marge brute 29.33% Marge bénéficiaire nette 0.80% Ratio dettes/capitaux propres 0%
Quelles ont été les performances à long terme de I1NC34?
Voir les performances historiques et les comparaisons
Analyse de l'entreprise et données financières Données Dernière mise à jour (heure UTC) Analyse de l'entreprise 2024/12/20 08:19 Cours de l'action en fin de journée 2024/11/27 00:00 Les revenus 2024/09/30 Revenus annuels 2023/12/31
Sources de données Les données utilisées dans notre analyse de l'entreprise proviennent de S&P Global Market Intelligence LLC . Les données suivantes sont utilisées dans notre modèle d'analyse pour générer ce rapport. Les données sont normalisées, ce qui peut entraîner un délai avant que la source ne soit disponible.
Paquet Données Cadre temporel Exemple de source américaine * Finances de l'entreprise 10 ans Compte de résultat Tableau des flux de trésorerie Bilan Estimations consensuelles des analystes +3 ans Prévisions financières Objectifs de prix des analystes Prix du marché 30 ans Cours des actions Dividendes, scissions et actions Propriété 10 ans Actionnaires principaux Délits d'initiés Gestion 10 ans L'équipe dirigeante Conseil d'administration Principaux développements 10 ans
* exemple pour les titres américains, pour les titres non-américains des formulaires et sources réglementaires équivalents sont utilisés.
Sauf indication contraire, toutes les données financières sont basées sur une période annuelle mais mises à jour trimestriellement. C'est ce qu'on appelle les données des douze derniers mois (TTM) ou des douze derniers mois (LTM). Pour en savoir plus , cliquez ici .
Modèle d'analyse et flocon de neige Les détails du modèle d'analyse utilisé pour générer ce rapport sont disponibles sur notre page Github . Nous avons également des guides sur la façon d'utiliser nos rapports et des tutoriels sur Youtube .
Découvrez l'équipe de classe mondiale qui a conçu et construit le modèle d'analyse Simply Wall St.
Indicateurs de l'industrie et du secteur Nos indicateurs de secteur et de section sont calculés toutes les 6 heures par Simply Wall St. Les détails de notre processus sont disponibles sur .
Sources des analystes Incyte Corporation est couverte par 55 analystes. 23 de ces analystes ont soumis les estimations de revenus ou de bénéfices utilisées comme données d'entrée dans notre rapport. Les soumissions des analystes sont mises à jour tout au long de la journée.
Analyste Institution Jasper Hellweg Argus Research Company Thomas Russo Baird Ishan Majumdar Baptista Research
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