GE91 주식 개요 젠맙 A/S는 주로 덴마크에서 암 및 기타 질병 치료를 위한 항체 치료제를 개발하는 회사입니다. 자세한 내용
생각, 링크 및 회사 내러티브를 캡처하세요.
가격 내역 및 성능
다음에 대한 주가 최고가, 최저가 및 변동 요약 Genmab 과거 주가 현재 주가 DKK 19.60 52주 최고치 DKK 29.80 52주 최저치 DKK 19.60 베타 0.87 1개월 변경 0% 3개월 변경 사항 -17.65% 1년 변경 사항 -30.50% 3년 변화 -43.68% 5년 변화 0.33% IPO 이후 변화 20.82%
최근 뉴스 및 업데이트
Genmab A/S Announces New Results from the Phase 1b/2 EPCORE NHL-2 Trial Dec 08
Genmab Announces New Data from the Phase 1/2 Study Of Rinatabart Sesutecan (Rina-S), an Investigational Folate Receptor-Alpha (FRa)-Targeted, Topo1 Antibody-Drug Conjugate Sep 16
Genmab A/S Receives Second European Commission Approval for the Treatment of Adults with Relapsed/Refractory Follicular Lymphoma Aug 20
Genmab A/S Announces Executive Changes Aug 16
Genmab A/S Takes Full Control of Acasunlimab Development Program Aug 06
Genmab A/S Announces That the U.S. Food and Drug Administration Approved Epkinly® (Epcoritamab-Bysp) for the Treatment of Adults with Relapsed or Refractory Follicular Lymphoma After Two or More Lines of Systemic EPKINLY Jun 27 더 많은 업데이트 보기
Genmab A/S Announces New Results from the Phase 1b/2 EPCORE NHL-2 Trial Dec 08
Genmab Announces New Data from the Phase 1/2 Study Of Rinatabart Sesutecan (Rina-S), an Investigational Folate Receptor-Alpha (FRa)-Targeted, Topo1 Antibody-Drug Conjugate Sep 16
Genmab A/S Receives Second European Commission Approval for the Treatment of Adults with Relapsed/Refractory Follicular Lymphoma Aug 20
Genmab A/S Announces Executive Changes Aug 16
Genmab A/S Takes Full Control of Acasunlimab Development Program Aug 06
Genmab A/S Announces That the U.S. Food and Drug Administration Approved Epkinly® (Epcoritamab-Bysp) for the Treatment of Adults with Relapsed or Refractory Follicular Lymphoma After Two or More Lines of Systemic EPKINLY Jun 27
Genmab A/S Announces New Efficacy and Safety Data from Two Ongoing Phase 1/2 Clinical Trials Evaluating Epcoritamab, A T-Cell Engaging Bispecific Antibody Administered Subcutaneously, in Adult Patients with Certain Types of Follicular Lymphoma Jun 05 Genmab A/S (CPSE:GMAB) completed the acquisition of ProfoundBio, Inc. May 22
Genmab A/S to Present New and Updated Results from Multiple Clinical Trials Evaluating Epcoritamab Across Various B-Cell Malignancies At the 2024 European Hematology Association (Eha) Congress May 15 Pfizer Inc. and Genmab A/S Announce FDA Grants Full Approval for TIVDAK to Treat Recurrent or Metastatic Cervical Cancer Apr 30
Genmab A/S (CPSE:GMAB) entered into a definitive agreement to acquire ProfoundBio for $1.8 billion. Apr 05
Genmab A/S (CPSE:GMAB) entered into a definitive agreement to acquire ProfoundBio for $1.8 billion. Apr 03
Genmab A/S Announces Executive Changes Mar 14 Genmab A/S and AbbVie Announce U.S. Food and Drug Administration Grants Priority Review for the Supplemental Biologics License Application for Epcoritamab (Epkinly®) for Difficult-To-Treat Relapsed or Refractory Follicular Lymphoma Feb 27
Genmab A/S and Pfizer, Inc. Announces Validation for Review the Marketing Authorization Application of Tivdak®? Feb 03
Genmab A/S Announces Decision in Arbitration Appeal Under License Agreement with Janssen Biotech, Inc Jan 23 Pfizer Inc. and Genmab A/S Announce U.S. Food and Drug Administration Accepts TIVDAK® Supplemental Biologics License Application Jan 10
Genmab A/S and AbbVie Announces New Pivotal Data for Bispecific Antibody Epcoritamab (Duobody CD3xCD20) Demonstrates High Overall and Complete Responses in Patients with Hard-To-Treat Relapsed/Refractory Follicular Lymphoma Dec 11
Genmab A/S Announces Positive Regulatory Updates for Epcoritamab (EPKINLY®?/TEPKINLY®?) for the Treatment of Relapsed/Refractory Follicular Lymphoma Nov 29
Genmab A/S Announces Positive Regulatory Updates for Epcoritamab (EPKINLY®?/TEPKINLY®?) for the Treatment of Relapsed/Refractory Follicular Lymphoma Nov 28
Genmab A/S Revises Earnings Guidance for the Year 2023 Nov 08
Genmab A/S, Annual General Meeting, Mar 13, 2024 Oct 28 Genmab A/S to Report Q1, 2024 Results on May 02, 2024 Genmab A/S and Seagen Inc. Announce Additional Results from the Phase 3 innovaTV 301 Randomized Global Trial Oct 24
Genmab A/S Announces European Commission Approval of Tepkinly(R) (epcoritamab) for Adults with Relapsed Or Refractory (R/R) Diffuse Large B-Cell Lymphoma (DLBCL) Seagen Inc. and Genmab A/S Announce That Tivdak(R) (Tisotumab Vedotin-Tftv) Met Its Primary Endpoint of Improved Overall Survival in Patients with Recurrent or Metastatic Cervical Cancer Compared to Chemotherapy Sep 05
Genmab A/S Revises Earning Guidance for the Year 2023 Jul 29
Genmab A/S Announces AbbVie Receives Positive CHMP Opinion for Epcoritamab (TEPKINLY(R) Diffuse Large B-Cell Lymphoma Jul 23 AbbVie and Genmab Announce Positive Topline Results from Phase 1/2 EPCORE™ NHL-1 Trial Evaluating Epcoritamab (DuoBody®-CD3xCD20) in Patients with Relapsed/Refractory Follicular Lymphoma (FL) Jun 28
Genmab A/S Announces Epcoritamab Added to National Comprehensive Cancer Network Clinical Practice Guidelines in Oncology for ‘B-Cell Lymphomas’ Jun 23
Genmab A/S Showcases Data from Comprehensive Epcoritamab Development Program in Patients Across B-Cell Lymphomas At European Hematology Association (EHA) Annual Meeting 2023 Jun 09
U.S. Food and Drug Administration Approves Genmab A/S’s EPKINLY (epcoritamab-bysp) as the First and Only Bispecific Antibody to Treat Adults with Relapsed or Refractory Diffuse Large B-cell Lymphoma May 20
Genmab A/S Provides Earnings Guidance for 2023 May 11
Genmab A/S Announces Submission of Japan New Drug Application for Epcoritamab (DuoBody®-CD3xCD20) for the Treatment of Relapsed/Refractory Large B-Cell Lymphoma Dec 22
Genmab A/S Showcases Data From Robust Development Program Evaluating Epcoritamab (DuoBody®-CD3xCD20) in Patients Across a Broad Range of B-Cell Lymphomas at the 64th Annual ASH Meeting Dec 13 Genmab A/S to Report Nine Months, 2023 Results on Nov 07, 2023
Genmab A/S Announces U.S. Food and Drug Administration Accepts for Priority Review Biologics License Application (Bla) for Epcoritamab (Duobody®-Cd3xcd20) for the Treatment of Relapsed/Refractory Large B-Cell Lymphoma (Lbcl) Nov 22 Genmab Provides Earnings Guidance for Year 2022
Genmab A/S Submits Biologics License Application to the U.S. Food and Drug Administration Oct 29
Genmab A/S Revises Earnings Guidance for the Year 2022 Aug 09
Genmab A/S Submits Biologics License Application to U.S. Food and Drug Administration for Epcoritamab for the Treatment of Relapsed/Refractory Large B-Cell Lymphoma Jul 01
Genmab Announces Late-Breaking Phase 2 Trial Results of Investigational Epcoritamab (DuoBody®-CD3xCD20) in Relapsed/Refractory Large B-cell Lymphoma (LBCL) Patients Presented at European Hematology Association (EHA) Presidential Symposium Jun 13
Genmab A/S and Seagen Inc. Present Data from Tisotumab Vedotin (TIVDAK) Clinical Development Program and Additional Cervical Cancer Research at ASCO 2022 Annual Meeting Jun 07
Genmab A/S Revises Earnings Guidance for 2022 May 12
AbbVie and Genmab Announce Topline Results for Epcoritamab (DuoBody®-CD3xCD20) from Phase 1/2 Trial in Patients with Relapsed/Refractory Large B-cell Lymphoma (LBCL) Apr 14
Genmab A/S Elects Elizabeth O’Farrell to the Board of Directors Mar 30
Genmab A/S Announces Appointments of Birgitte Stephensen to Chief Legal Officer and Chris Cozic to Chief People Officer Mar 03
Genmab A/S Provides Earnings Guidance for the Year 2022 Feb 18
Genmab A/S Provides Earnings Guidance for the Year 2022 Feb 17
Genmab A/S Announces Janssen Received Conditional European Marketing Authorization for RYBREVANT Dec 15
U.S. Food and Drug Administration Grants Approval to TIVDAK Sep 24 Seagen Inc. and Genmab A/S Announce FDA Accelerated Approval for TIVDAK™ (Tisotumab Vedotin-Tftv) in Previously Treated Recurrent or Metastatic Cervical Cancer
Genmab A/S Announces the Lancet Published the Results of FIH Trial Sep 10
Genmab A/S Improves Revenue Guidance for the Full Year of Fiscal 2021 Aug 12
Genmab A/S Announces That Janssen Has Received European Marketing Authorizations for Darzalex® (Daratumumab) Subcutaneous Formulation, Including for the Treatment of Patients with Newly Diagnosed Light-Chain (Al) Amyloidosis Jun 23 Genmab Announces Janssen Received Positive CHMP Opinion Recommending DARZALEX (daratumumab) Subcutaneous (SC) Formulation for Patients with Newly Diagnosed Light-chain (AL) Amyloidosis
Genmab Announces Abstracts Evaluating Products in Pipeline, Portfolio to be Presented at American Society of Clinical Oncology (ASCO) Annual Meeting and European Hematology Association (EHA) Congress May 21
Genmab A/S Reaffirms Financial Guidance for Fiscal 2021 May 06
Genmab A/S Provides Revenue Guidance for the Full Year of Fiscal 2021 Apr 15
Genmab Announces Appointment of Tahamtan Ahmadi to Newly Created Position of Chief Medical Officer, Head of Experimental Medicines Feb 23
Seagen Inc. and Genmab A/S Submit Tisotumab Vedotin Biologics License Application to the U.S. FDA for Patients with Recurrent or Metastatic Cervical Cancer Feb 11 주주 수익률 GE91 DE Biotechs DE 마켓 7D 0% -1.2% -1.4% 1Y -30.5% -13.2% 8.0%
전체 주주 수익률 보기
수익률 대 산업: GE91 지난 1년 동안 -13.2 %를 반환한 German Biotechs 업계보다 저조한 성과를 냈습니다.
수익률 대 시장: GE91 지난 1년 동안 8 %를 반환한 German 시장보다 저조한 성과를 냈습니다.
가격 변동성 Is GE91's price volatile compared to industry and market? GE91 volatility GE91 Average Weekly Movement n/a Biotechs Industry Average Movement 6.7% Market Average Movement 4.9% 10% most volatile stocks in DE Market 11.9% 10% least volatile stocks in DE Market 2.5%
안정적인 주가: GE91 의 주가는 지난 3개월 동안 변동성이 심했습니다.
시간에 따른 변동성: 지난 1년간 GE91 의 변동성 변화를 확인하기에는 데이터가 충분하지 않습니다 .
회사 소개 젠맙 A/S는 주로 덴마크에서 암 및 기타 질병 치료를 위한 항체 치료제를 개발합니다. 이 회사는 다발성 골수종(MM) 환자 치료를 위한 인간 단일 클론 항체인 다잘렉스(DARZALEX), 갑상선 안질환 치료를 위한 테프로투무맙, 진행성 또는 전이성 위암 또는 식도암과 비소세포폐암을 위한 아미반타맙을 판매하고 있습니다. 다라투무맙은 다발골수성 백혈병, 비다발골수성 백혈병 및 AL 아밀로이드증 치료제로, GEN1047, 티소투맙 베도틴은 자궁경부암, 난소암 및 고형암 치료제로, 듀오바디-PD-L1x4-1BB 및 듀오바디-CD40x4-1BB는 고형 종양 치료제로 사용됩니다; 재발성/불응성 미만성 거대 B세포 림프종 및 만성 림프구성 백혈병 치료를 위한 엡코리타맙, 혈액암 치료를 위한 HexaBody-CD38 및 GEN3017.
자세히 보기 Genmab A/S 기본 사항 요약 Genmab 의 수익과 매출은 시가총액과 어떻게 비교하나요? GE91 기본 통계 시가총액 €12.15b 수익(TTM ) €630.25m 수익(TTM ) €2.66b
수익 및 수익 최신 수익 보고서의 주요 수익성 통계(TTM) GE91 손익 계산서(TTM ) 수익 DKK 19.84b 수익 비용 DKK 774.00m 총 이익 DKK 19.07b 기타 비용 DKK 14.37b 수익 DKK 4.70b
주당 순이익(EPS) 74.02 총 마진 96.10% 순이익 마진 23.69% 부채/자본 비율 0%
GE91 의 장기적인 성과는 어땠나요?
과거 실적 및 비교 보기
기업 분석 및 재무 데이터 현황 데이터 마지막 업데이트(UTC 시간) 기업 분석 2024/12/18 11:48 장 마감 주가 2024/11/15 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.
Simply 월스트리트 분석 모델을 설계하고 구축한 세계적인 수준의 팀에 대해 알아보세요.
산업 및 부문 메트릭 업계 및 섹션 지표는 Simply Wall St에서 6시간마다 계산되며, 자세한 내용은 확인할 수 있습니다.
애널리스트 출처 Genmab A/S 45 애널리스트 중 23 애널리스트가 보고서의 입력 자료로 사용된 매출 또는 수익 추정치를 제출했습니다. 애널리스트의 제출 자료는 하루 종일 업데이트됩니다.
분석가 교육기관 Andrew Carlsen ABG Sundal Collier Armelle Moulin AlphaValue Emily Field Barclays
42 더 많은 분석가 보기 
