Genmab Yönetim

Yönetim kriter kontrolleri 3/4

Genmab CEO'su Jan G.J. de Winkel, Jun2010 tarihinde atandı, in görev süresi 15.75 yıldır. in toplam yıllık tazminatı $ 10.70M olup, şirket hissesi ve opsiyonları dahil olmak üzere 14% maaş ve 86% ikramiyelerden oluşmaktadır. şirketin hisselerinin 1.07% ine doğrudan sahiptir ve bu hisseler $ 183.24M değerindedir. Yönetim ekibinin ve yönetim kurulunun ortalama görev süresi sırasıyla 6 yıl ve 8 yıldır.

Anahtar bilgiler

Jan G.J. de Winkel

İcra Kurulu Başkanı

US$10.7m

Toplam tazminat

CEO maaş yüzdesi	14.02%
CEO görev süresi	15.8yrs
CEO sahipliği	1.1%
Yönetim ortalama görev süresi	6yrs
Yönetim Kurulu ortalama görev süresi	8yrs

Son yönetim güncellemeleri

Recent updates

CEO Tazminat Analizi

Jan G.J. de Winkel'un ücretlendirmesi Genmab'un kazancına kıyasla nasıl değişti?
Tarih	Toplam Tazminat	Maaş	Şirket Kazançları
Dec 31 2025	US$11m	US$2m	US$963m
Sep 30 2025	n/a	n/a	US$2b
Jun 30 2025	n/a	n/a	US$1b
Mar 31 2025	n/a	n/a	US$1b
Dec 31 2024	US$8m	US$1m	US$1b
Sep 30 2024	n/a	n/a	US$702m
Jun 30 2024	n/a	n/a	US$798m
Mar 31 2024	n/a	n/a	US$791m
Jan 01 2024	n/a	n/a	US$631m
Sep 30 2023	n/a	n/a	US$590m
Jun 30 2023	n/a	n/a	US$680m
Mar 31 2023	n/a	n/a	US$757m
Dec 31 2022	US$6m	US$1m	US$785m
Sep 30 2022	n/a	n/a	US$745m
Jun 30 2022	n/a	n/a	US$558m
Mar 31 2022	n/a	n/a	US$354m
Dec 31 2021	US$6m	US$1m	US$452m
Sep 30 2021	n/a	n/a	US$448m
Jun 30 2021	n/a	n/a	US$401m
Mar 31 2021	n/a	n/a	US$880m
Dec 31 2020	US$6m	US$1m	US$781m
Sep 30 2020	n/a	n/a	US$889m
Jun 30 2020	n/a	n/a	US$853m
Mar 31 2020	n/a	n/a	US$349m
Dec 31 2019	US$5m	US$1m	US$325m

Tazminat ve Piyasa: Jan G.J. 'ın toplam tazminatı ($USD 10.70M ) US pazarındaki benzer büyüklükteki şirketler için ortalamadır ($USD 13.43M ).

Tazminat ve Kazançlar: Jan G.J. şirketinin tazminatı %20'den fazla artarken, şirketin kazancı geçen yıl %20'den fazla düştü.

CEO

Jan G.J. de Winkel (64 yo)

15.8yrs

Görev süresi

US$10,700,000

Tazminat

Dr. Jan G.J. van de Winkel, Ph.D. was Independent Director of HOOKIPA Pharma Inc. from 2023 until August 30, 2024 and served as Chairman of the Board since 2024 August 30, 2024. Dr. Winkel served as a Memb...

Liderlik Ekibi

İsim	Pozisyon	Görev süresi	Tazminat	Sahiplik
Jan G.J. de Winkel	Co-Founder	15.8yrs	US$10.70m	1.07% $ 183.2m
Anthony Pagano	Executive VP & CFO	6yrs	US$4.70m	0.0096% $ 1.6m
Rayne Waller	Executive VP & Chief Technical Operations Officer	1.6yrs	US$2.70m	Veri yok
Gregory David Mueller	Executive VP	less than a year	US$1.80m	Veri yok
Christopher Cozic	Executive VP & Chief People Officer	8.3yrs	US$3.40m	Veri yok
Martine van Vugt	Executive VP & Chief Strategy Officer	12.2yrs	US$2.40m	Veri yok
Martin Schultz	Senior Director	no data	US$300.00k	0.0011% $ 186.4k
Judith Klimovsky	Executive VP & Chief Development Officer	9.1yrs	US$5.40m	0.018% $ 3.0m
Tahamtan Ahmadi	Executive VP	5yrs	US$5.20m	0.0079% $ 1.4m
Mijke Zachariasse	VP, Head of Antibody Research Materials & Director	no data	US$300.00k	0.0013% $ 218.9k
Takahiro Hamatani	Senior Director of Finance Japan & Non-Independent Director	no data	US$100.00k	0.00013% $ 22.2k
Brad Bailey	Executive VP & Chief Commercial Officer	1.6yrs	US$2.10m	Veri yok

6.0yrs

Ortalama Görev Süresi

53yo

Ortalama Yaş

Deneyimli Yönetim: GNMS.F 'un yönetim ekibi deneyimli ve deneyimlidir ( 6 yıldır).

Yönetim Kurulu Üyeleri

İsim	Pozisyon	Görev süresi	Tazminat	Sahiplik
Martin Schultz	Senior Director	4.2yrs	US$300.00k	0.0011% $ 186.4k
Mijke Zachariasse	VP, Head of Antibody Research Materials & Director	7yrs	US$300.00k	0.0013% $ 218.9k
Takahiro Hamatani	Senior Director of Finance Japan & Non-Independent Director	4.2yrs	US$100.00k	0.00013% $ 22.2k
Michael Kavanagh	Senior Director	1.2yrs	US$200.00k	0.00036% $ 61.6k
Anders Pedersen	Non-Independent Director	22.3yrs	US$400.00k	0.013% $ 2.1m
Elizabeth O'Farrell	Independent Director	4yrs	US$400.00k	0.0031% $ 524.9k
Deirdre Connelly	Independent Chairman of the Board	9yrs	US$600.00k	0.011% $ 1.8m
Rolf Hoffmann	Independent Director	9yrs	US$400.00k	0.0062% $ 1.1m
Pernille Erenbjerg	Independent Deputy Chairman	11.2yrs	US$400.00k	0.0089% $ 1.5m
Paolo Paoletti	Independent Director	11.2yrs	US$300.00k	0.0041% $ 697.6k

8.0yrs

Ortalama Görev Süresi

59.5yo

Ortalama Yaş

Deneyimli Yönetim Kurulu: GNMS.F 'nin yönetim kurulu üyeleri deneyimli olarak kabul edilir (ortalama görev süresi 8 yıldır).

Şirket Analizi ve Finansal Veri Durumu

Veri	Son Güncelleme (UTC saati)
Şirket Analizi	2026/03/05 20:51
Gün Sonu Hisse Fiyatı	2026/02/24 00:00
Kazançlar	2025/12/31
Yıllık Kazançlar	2025/12/31

Veri Kaynakları

Şirket analizimizde kullanılan veriler S&P Global Market Intelligence LLC'den alınmıştır. Bu raporu oluşturmak için analiz modelimizde aşağıdaki veriler kullanılmıştır. Veriler normalize edilmiştir, bu da kaynağın mevcut olmasından kaynaklanan bir gecikmeye neden olabilir.

Paket	Veri	Zaman Çerçevesi	Örnek ABD Kaynağı ^*
Şirket Finansalları	10 yıl	Gelir tablosu Nakit akış tablosu Bilanço	SEC Form 10-K SEC Form 10-Q
Analist Konsensüs Tahminleri	+3 yıl	Finansal tahminler Analist fiyat hedefleri	Analist Araştırma Raporları Blue Matrix
Piyasa Fiyatları	30 yıl	Hisse senedi fiyatları Temettüler, Bölünmeler ve Eylemler	ICE Piyasa Verileri SEC Form S-1
Sahiplik	10 yıl	En büyük hissedarlar İçeriden öğrenenlerin ticareti	SEC Form 4 SEC Form 13D
Yönetim	10 yıl	Liderlik ekibi Yönetim Kurulu	SEC Form 10-K SEC Form DEF 14A
Önemli Gelişmeler	10 yıl	Şirket duyuruları	SEC Form 8-K

* ABD menkul kıymetleri için örnek, ABD dışı için eşdeğer düzenleyici formlar ve kaynaklar kullanılmıştır.

Belirtilmediği sürece tüm finansal veriler yıllık bir döneme dayanmaktadır ancak üç ayda bir güncellenmektedir. Bu, İzleyen On İki Ay (TTM) veya Son On İki Ay (LTM) Verileri olarak bilinir. Daha fazla bilgi edinin.

Analiz Modeli ve Kar Tanesi

Bu raporu oluşturmak için kullanılan analiz modelinin ayrıntıları Github sayfamızda mevcuttur, raporlarımızı nasıl kullanacağınız konusunda kılavuzlarımız ve Youtube'da eğitim videolarımız da bulunmaktadır.

Simply Wall St analiz modelini tasarlayan ve oluşturan dünya standartlarındaki ekip hakkında bilgi edinin.

Endüstri ve Sektör Metrikleri

Sektör ve bölüm metriklerimiz Simply Wall St tarafından her 6 saatte bir hesaplanmaktadır, sürecimizin ayrıntıları Github'da mevcuttur.

Analist Kaynakları

Genmab A/S 36 Bu analistlerden 16, raporumuzun girdisi olarak kullanılan gelir veya kazanç tahminlerini sunmuştur. Analistlerin gönderimleri gün boyunca güncellenmektedir.

Analist	Kurum
Emily Field	Barclays
James Gordon	Barclays
Xue Chen	Barclays

Genmab Yönetim

Yönetim kriter kontrolleri 3/4

Anahtar bilgiler

Son yönetim güncellemeleri

Genmab A/S, Annual General Meeting, Mar 19, 2026

Genmab Announces Changes to Its Executive Committee

Genmab A/S, Annual General Meeting, Mar 12, 2025

Genmab A/S Announces Executive Changes

Genmab A/S Announces Executive Changes

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

Recent updates

Genmab A/S, Annual General Meeting, Mar 19, 2026

Genmab Provides Earnings Guidance for the Full Year 2026

Genmab A/S Announces Topline Results for Epcoritamab (DuoBody CD3xCD20) from Phase 3 EPCORE DLBCL-1 Trial in Patients with Relapsed Refractory Diffuse Large B-Cell Lymphoma

Genmab A/S to Discontinue Further Clinical Development of Acasunlimab Following A Portfolio Review

Genmab A/S (CPSE:GMAB) completed the acquisition of Merus N.V. (NasdaqGM:MRUS) in a tender offer transaction.

Genmab A/S Announces EPKINLY (epcoritamab-bysp) in Combination with Rituximab and Lenalidomide Approved by the U.S. Food and Drug Administration for the Treatment of Relapsed or Refractory Follicular Lymphoma

Genmab A/S to Report First Half, 2026 Results on Aug 06, 2026

Genmab Provides Earnings Guidance for the Full Year 2025

Genmab A/S Announces New Data Demonstrating Investigational Rinatabart Sesutecan (Rina-S®?) Achieved Anti-Tumor Activity in Heavily Pretreated Patients with Advanced Endometrial Cancer

Genmab Reportedly in Advanced Talks to Buy Merus

Genmab A/S Announces Updated Results from Phase 2 Epcore®? Nhl-6 Study Evaluating Epcoritamab Monotherapy in the Outpatient Setting in Patients with Relapsed/Refractory (R/R) Diffuse Large B-Cell Lymphoma (Dlbcl)

Genmab A/S Raises Earnings Guidance for the Year 2025

Genmab Announces Changes to Its Executive Committee

Genmab A/S Announces Investigational Rinatabart Sesutecan (Rina-S) Demonstrates Encouraging Anti-Tumor Activity Heavily Pretreated Patients with Advanced Endometrial Cancer in Phase 1/2 RAINFOL-01 Trial

Genmab A/S to Present New and Updated Results from Its Robust Epcoritamab (Epkinly®) Development Program At the 2025 European Hematology Association (Eha) Congress

Genmab A/S to Submit Supplemental Biologics License Application (sBLA) to U.S. Food and Drug Administration for Epcoritamab Plus Rituximab and Lenalidomide (R2) in Patients with Relapsed Refractory Follicular Lymphoma

Genmab A/S Announces Japan Ministry of Health, Labour and Welfare Approves TIVDAK for the Treatment of Advanced or Recurrent Cervical Cancer

Genmab A/S Updates Data from Cohort B1 of the Phase 1/2 RAINFOL-01 Study of Rina-S

Genmab A/S, Annual General Meeting, Mar 12, 2025

Genmab A/S Provides Revenue Guidance for 2025

Genmab A/S Announces New Results from the Phase 1b/2 EPCORE NHL-2 Trial

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 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 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 to Report Nine Months, 2023 Results on Nov 07, 2023

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

CEO Tazminat Analizi

CEO

Liderlik Ekibi

Yönetim Kurulu Üyeleri

Şirket Analizi ve Finansal Veri Durumu

Veri Kaynakları

Analiz Modeli ve Kar Tanesi

Endüstri ve Sektör Metrikleri

Analist Kaynakları