Genmab (BST:GE91) - Cours de l'action, nouvelles et analyse

GE91 Aperçu des actions

Genmab A/S développe des anticorps thérapeutiques pour le traitement du cancer et d'autres maladies, principalement au Danemark. Plus de détails

GE91 analyse fondamentale
Score flocon de neige
Évaluation	5/6
Croissance future	4/6
Performances passées	4/6
Santé financière	6/6
Dividendes	0/6

Récompenses

Se négocie à 84.8% en dessous de notre estimation de sa juste valeur

Les bénéfices devraient augmenter 23.73% par an

Les bénéfices ont augmenté de 12.9% au cours de l'année écoulée

Se négocie à un bon prix par rapport à ses pairs et au secteur

Analyse des risques

Aucun risque n'a été détecté pour GE91 à partir de nos contrôles de risques.

Genmab A/S Concurrents

Biotest

XTRA:BIO3

€1.4b

Formycon

XTRA:FYB

€818.4m

Sartorius

XTRA:SRT3

€13.4b

SCHOTT Pharma KGaA

XTRA:1SXP

€4.0b

Historique des prix et performances

Résumé des plus hauts, des changements et des baisses de prix pour Genmab
Historique des cours de bourse
Prix actuel de l'action	DKK 19.60
Plus haut sur 52 semaines	DKK 30.20
Plus bas sur 52 semaines	DKK 19.60
Bêta	0.86
1Variation sur 1 mois	-9.26%
Variation sur 3 mois	-17.65%
Variation sur 1 an	-34.67%
3Variation sur 3 ans	-46.45%
Variation sur 5 ans	-6.06%
Évolution depuis l'introduction en bourse	20.82%

Nouvelles et mises à jour récentes

Recent updates

Rendement pour les actionnaires

	GE91	DE Biotechs	DE Marché
7D	-7.5%	-1.0%	-0.5%
1Y	-34.7%	-16.7%	8.3%

Rendement vs Industrie: GE91 a sous-performé le secteur German Biotechs qui a rapporté -16.7 % au cours de l'année écoulée.

Rendement vs marché: GE91 a sous-performé le marché German qui a rapporté 8.3 % au cours de l'année écoulée.

Volatilité des prix

Is GE91's price volatile compared to industry and market?
GE91 volatility
GE91 Average Weekly Movement	n/a
Biotechs Industry Average Movement	6.4%
Market Average Movement	4.8%
10% most volatile stocks in DE Market	11.0%
10% least volatile stocks in DE Market	2.4%

Cours de l'action stable: Les données ne sont pas disponibles.

Volatilité au fil du temps: Données insuffisantes pour déterminer l'évolution de la volatilité de GE91 au cours de l'année écoulée.

À propos de l'entreprise

Fondée	Salariés	PDG	Site web
1999	2,635	Jan G.J. de Winkel	www.genmab.com

Genmab A/S développe des anticorps thérapeutiques pour le traitement du cancer et d'autres maladies, principalement au Danemark. La société commercialise DARZALEX, un anticorps monoclonal humain pour le traitement des patients atteints de myélome multiple (MM), le teprotumumab pour le traitement des maladies oculaires de la thyroïde et l'amivantamab pour le traitement du cancer gastrique ou œsophagien avancé ou métastatique et du cancer du poumon non à petites cellules (NSCLC). Ses produits comprennent le daratumumab pour traiter le MM, les cancers du sang non-MM et l'amylose AL ; GEN1047 ; le tisotumab vedotin pour traiter les cancers du col de l'utérus, de l'ovaire et les cancers solides ; DuoBody-PD-L1x4-1BB, et DuoBody-CD40x4-1BB pour traiter les tumeurs solides ; Epcoritamab pour le traitement du lymphome diffus à grandes cellules B récidivant/réfractaire et de la leucémie lymphocytaire chronique ; et HexaBody-CD38 et GEN3017 pour le traitement des hémopathies malignes.

Genmab A/S Résumé des fondamentaux

Comment les bénéfices et les revenus de Genmab se comparent-ils à sa capitalisation boursière ?
GE91 statistiques fondamentales
Capitalisation boursière	€12.35b
Bénéfices(TTM)	€630.34m
Recettes(TTM)	€2.66b

19.6x

Ratio P/E

4.6x

Ratio P/S

Le site GE91 est-il surévalué ?

Voir Juste valeur et analyse de l'évaluation

Bénéfices et recettes

Principales statistiques de rentabilité tirées du dernier rapport sur les bénéfices (TTM)
GE91 compte de résultat (TTM)
Recettes	DKK 19.84b
Coût des recettes	DKK 774.00m
Marge brute	DKK 19.07b
Autres dépenses	DKK 14.37b
Les revenus	DKK 4.70b

Derniers bénéfices déclarés

Sep 30, 2024

Prochaine date de publication des résultats

s/o

Résultat par action (EPS)	74.03
Marge brute	96.10%
Marge bénéficiaire nette	23.69%
Ratio dettes/capitaux propres	0%

Quelles ont été les performances à long terme de GE91?

Voir les performances historiques et les comparaisons

GE91 Aperçu des actions

Récompenses

Analyse des risques

Genmab A/S Concurrents

XTRA:BIO3

€1.4b

XTRA:FYB

€818.4m

XTRA:SRT3

€13.4b

XTRA:1SXP

€4.0b

Historique des prix et performances

Nouvelles et mises à jour récentes

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

Genmab A/S Receives Second European Commission Approval for the Treatment of Adults with Relapsed/Refractory Follicular Lymphoma

Genmab A/S Announces Executive Changes

Genmab A/S Takes Full Control of Acasunlimab Development Program

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

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

Recent updates

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

Genmab A/S Receives Second European Commission Approval for the Treatment of Adults with Relapsed/Refractory Follicular Lymphoma

Genmab A/S Announces Executive Changes

Genmab A/S Takes Full Control of Acasunlimab Development Program

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

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

Genmab A/S (CPSE:GMAB) completed the acquisition of ProfoundBio, Inc.

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

Pfizer Inc. and Genmab A/S Announce FDA Grants Full Approval for TIVDAK to Treat Recurrent or Metastatic Cervical Cancer

Genmab A/S (CPSE:GMAB) entered into a definitive agreement to acquire ProfoundBio for $1.8 billion.

Genmab A/S (CPSE:GMAB) entered into a definitive agreement to acquire ProfoundBio for $1.8 billion.

Genmab A/S Announces Executive Changes

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

Genmab A/S and Pfizer, Inc. Announces Validation for Review the Marketing Authorization Application of Tivdak®?

Genmab A/S Announces Decision in Arbitration Appeal Under License Agreement with Janssen Biotech, Inc

Pfizer Inc. and Genmab A/S Announce U.S. Food and Drug Administration Accepts TIVDAK® Supplemental Biologics License Application

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

Genmab A/S Announces Positive Regulatory Updates for Epcoritamab (EPKINLY®?/TEPKINLY®?) for the Treatment of Relapsed/Refractory Follicular Lymphoma

Genmab A/S Announces Positive Regulatory Updates for Epcoritamab (EPKINLY®?/TEPKINLY®?) for the Treatment of Relapsed/Refractory Follicular Lymphoma

Genmab A/S Revises Earnings Guidance for the Year 2023

Genmab A/S, Annual General Meeting, Mar 13, 2024

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

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

Genmab A/S Revises Earning Guidance for the Year 2023

Genmab A/S Announces AbbVie Receives Positive CHMP Opinion for Epcoritamab (TEPKINLY(R) Diffuse Large B-Cell Lymphoma

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)

Genmab A/S Announces Epcoritamab Added to National Comprehensive Cancer Network Clinical Practice Guidelines in Oncology for ‘B-Cell Lymphomas’

Genmab A/S Showcases Data from Comprehensive Epcoritamab Development Program in Patients Across B-Cell Lymphomas At European Hematology Association (EHA) Annual Meeting 2023

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

Genmab A/S Provides Earnings Guidance for 2023

Genmab A/S Announces Submission of Japan New Drug Application for Epcoritamab (DuoBody®-CD3xCD20) for the Treatment of Relapsed/Refractory Large B-Cell Lymphoma

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

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)

Genmab Provides Earnings Guidance for Year 2022

Genmab A/S Submits Biologics License Application to the U.S. Food and Drug Administration

Genmab A/S Revises Earnings Guidance for the Year 2022

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

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

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

Genmab A/S Revises Earnings Guidance for 2022

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)

Genmab A/S Elects Elizabeth O’Farrell to the Board of Directors

Genmab A/S Announces Appointments of Birgitte Stephensen to Chief Legal Officer and Chris Cozic to Chief People Officer

Genmab A/S Provides Earnings Guidance for the Year 2022

Genmab A/S Provides Earnings Guidance for the Year 2022

Genmab A/S Announces Janssen Received Conditional European Marketing Authorization for RYBREVANT

U.S. Food and Drug Administration Grants Approval to TIVDAK

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

Genmab A/S Improves Revenue Guidance for the Full Year of Fiscal 2021

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

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

Genmab A/S Reaffirms Financial Guidance for Fiscal 2021

Genmab A/S Provides Revenue Guidance for the Full Year of Fiscal 2021

Genmab Announces Appointment of Tahamtan Ahmadi to Newly Created Position of Chief Medical Officer, Head of Experimental Medicines