Overall impact
A (80)

Commentary

Genmab is a leader for overall positive impact. With an 'A' rating of 80.3 for overall impact (94th percentile compared to all companies), Genmab ranks 48th out of 585 industry peers, behind Amgen, Regeneron Pharmaceuticals, Cell Source and 44 others, and ahead of Grifols, Biogen, Ionis Pharmaceuticals and 534 others. On top material causes for Genmab's industry (Pharmaceuticals & Biotech), Genmab performs well in Equal Pay and Opportunity (95.7 score), Accountable Institutions (84.3), Technology Innovation (95.5) and 8 other causes where it received an 'A' score and performs poorly in Humane Treatment of Animals (0.3 score), Sustainable Use of Water (34.1) and Reduced Use of tobacco (38.3).
Impact
Cause GMAB
Peer rank
Overall impact

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Company
Founded
1999
Employees
2,973
Sector
Health Care
Industry
Biotechnology
Sub-industry
Biotechnology
SASB industry
Biotechnology & Pharmaceuticals
Headquarters
Denmark
Share classes
GMAB
Description
Genmab A/S, a biotechnology company, develops antibody-based products and product candidates for the treatment of cancer and other diseases in Denmark. The company markets EPKINLY and TEPKINLY for adult patients with relapsed or refractory (R/R) diffuse large b-cell lymphoma (DLBCL), large Bcell lymphoma, and follicular lymphoma (FL); and Tivdak for adult patients with recurrent/metastatic cervical cancer with disease progression on or after chemotherapy. It is also developing Epcoritamab for R/R DLBCL and FL, first line DLBCL and FL, B-cell non-Hodgkin lymphoma, R/R chronic lymphocytic leukemia and Richter's syndrome, and aggressive mature B-cell neoplasms in pediatric patients; tisotumab vedotin for solid tumors; Acasunlimab for solid tumors and non-small cell lung cancer (NSCLC); Rinatabart Sesutecan for platinum resistant ovarian cancer and solid tumors; GEN1042, GEN1059, GEN1055, and GEN1057 for solid tumors; GEN3014 for hematologic malignancies; GEN1160 for advanced solid and liquid tumors; and GEN1107 and GEN1286 for advanced solid tumors. In addition, the company offers DARZALEX/DARZALEX FASPRO for multiple myeloma (MM) and light-chain Amyloidosis; RYBREVANT for NSCLC; TECVAYLI and TALVEY for R/R MM; Kesimpta for Relapsing multiple sclerosis; and TEPEZZA for thyroid eye disease. Further, it is developing Amivantamab for recurrent/metastatic head and neck cancer, and advanced or metastatic colorectal cancer; Amlenetug for multiple system atrophy; Inclacumab for vaso-occulsive crises in sickle cell diseases; and Mim8 for hemophilia A. The company has a collaboration agreement with AbbVie Inc., Pfizer Inc., BioNTech SE, Johnson & Johnson, Novartis International AG, Medarex, Inc., ADC Therapeutics SA, Bristol Myers Squibb Corporation, Lundbeck A/S, Amgen Inc., Immatics, Novo Nordisk A/S, CureVac AG, and argenx. Genmab A/S was incorporated in 1998 and is headquartered in Copenhagen, Denmark.
Material causes
Ethos considers the following causes material for Genmab, based on its industry sub-industry Biotechnology. Learn more about material causes in our methodology overview.

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