I1NC34 주식 개요 바이오 제약 회사인 Incyte Corporation은 미국 및 전 세계에서 혈액학/종양학, 염증 및 자가 면역 분야의 치료제를 발견, 개발 및 상업화하는 데 관여하고 있습니다. 자세한 내용
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가격 내역 및 성능
다음에 대한 주가 최고가, 최저가 및 변동 요약 Incyte 과거 주가 현재 주가 US$221.76 52주 최고치 US$232.20 52주 최저치 US$135.90 베타 0.70 1개월 변경 0% 3개월 변경 사항 22.10% 1년 변경 사항 n/a 3년 변화 4.64% 5년 변화 n/a IPO 이후 변화 38.34%
최근 뉴스 및 업데이트
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 더 많은 업데이트 보기
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 주주 수익률 I1NC34 BR Biotechs BR 마켓 7D 0% 0.6% -2.2% 1Y n/a -3.6% -14.8%
전체 주주 수익률 보기
수익률 대 산업: BR Biotechs 산업에 대해 I1NC34 의 성과를 판단하기에는 데이터가 부족합니다.
수익률 대 시장: BR 시장에 대해 I1NC34 의 성과를 판단하기에는 데이터가 부족합니다.
가격 변동성 Is I1NC34's price volatile compared to industry and market? I1NC34 volatility I1NC34 Average Weekly Movement n/a Biotechs Industry Average Movement 9.2% Market Average Movement 5.1% 10% most volatile stocks in BR Market 9.7% 10% least volatile stocks in BR Market 3.0%
안정적인 주가: I1NC34 의 주가는 지난 3개월 동안 변동성이 심했습니다.
시간에 따른 변동성: 지난 1년간 I1NC34 의 변동성 변화를 확인하기에는 데이터가 충분하지 않습니다 .
회사 소개 바이오 제약 회사인 인사이트 코퍼레이션은 미국 및 전 세계에서 혈액학/종양학, 염증 및 자가 면역 분야의 치료제를 발견, 개발 및 상업화하는 기업입니다. 이 회사는 중등도 또는 고위험 골수섬유증, 적혈구증가증, 스테로이드 불응성 급성 이식편대숙주질환 치료를 위한 자카피(성분명 룩소리티닙)를 제공합니다; 재발성 또는 불응성 미만성 거대 B세포 림프종 치료제 '몬주비'(타파시타맙-cxix)/민주비(타파시타맙), 액체 및 고형 종양 유형에서 발암 요인으로 작용하는 섬유아세포 성장인자 수용체 키나제 억제제 '페마자이어'(페미가티닙); 만성 골수성 백혈병 및 필라델피아 염색체 양성 급성 림프모구 백혈병 치료제 아이클루시그(포나티닙), 전이성 또는 재발성 국소 진행성 메르켈세포암 성인 치료제 자이닉스(레티판리맙-dlwr), 아토피 피부염 치료제 옵젤루라 크림 등이 있습니다. 임상 단계 제품으로는 항문관 편평상피세포암 및 비소세포폐암 치료제로 임상 3상 중인 레티판리맙, 만성 이식편대숙주질환 환자 치료제로 개발 중인 2상 항-CSF-1R 단일클론항체 악사틸리맙, 종양 발생 억제제 INCA033989, 질병 조절 치료제로 개발 중인 INCB160058, 고형암 치료용 INCB99280 및 INCB99318 등이 있습니다.
자세히 보기 Incyte Corporation 기본 사항 요약 Incyte 의 수익과 매출은 시가총액과 어떻게 비교하나요? I1NC34 기본 통계 시가총액 R$82.56b 수익(TTM ) R$201.07m 수익(TTM ) R$25.23b
수익 및 수익 최신 수익 보고서의 주요 수익성 통계(TTM) I1NC34 손익 계산서(TTM ) 수익 US$4.08b 수익 비용 US$2.88b 총 이익 US$1.20b 기타 비용 US$1.16b 수익 US$32.48m
주당 순이익(EPS) 0.17 총 마진 29.33% 순이익 마진 0.80% 부채/자본 비율 0%
I1NC34 의 장기적인 성과는 어땠나요?
과거 실적 및 비교 보기
기업 분석 및 재무 데이터 현황 데이터 마지막 업데이트(UTC 시간) 기업 분석 2024/12/29 11:39 장 마감 주가 2024/11/27 00:00 수익 2024/09/30 연간 수익 2023/12/31
데이터 소스 기업 분석에 사용된 데이터는 S&P Global Market Intelligence LLC의 데이터입니다. 이 보고서를 생성하기 위해 분석 모델에 사용된 데이터는 다음과 같습니다. 데이터는 정규화되어 있으므로 소스가 제공되기까지 지연이 발생할 수 있습니다.
패키지 데이터 기간 미국 소스 예시 * 회사 재무 10년 애널리스트 컨센서스 추정치 +3년 시장 가격 30년 소유권 10년 관리 10년 주요 개발 사항 10년
* 미국 증권의 경우, 미국 외 지역의 규제 양식 및 출처가 사용된 예입니다.
명시되지 않는 한 모든 재무 데이터는 1년을 기준으로 하지만 분기별로 업데이트됩니다. 이를 후행 12개월(TTM) 또는 최근 12개월(LTM) 데이터라고 합니다. 여기에서 자세히 알아보세요.
분석 모델 및 눈송이 이 보고서를 생성하는 데 사용된 분석 모델에 대한 자세한 내용은 Github 페이지에서 확인할 수 있으며, 보고서 사용 방법에 대한 가이드와 튜토리얼도 유튜브에서 확인할 수 있습니다.
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애널리스트 출처 Incyte Corporation 54 애널리스트 중 23 애널리스트가 보고서의 입력 자료로 사용된 매출 또는 수익 추정치를 제출했습니다. 애널리스트의 제출 자료는 하루 종일 업데이트됩니다.
분석가 교육기관 Jasper Hellweg Argus Research Company Thomas Russo Baird Ishan Majumdar Baptista Research
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