Genmab A/S - ADR (OQ:GMAB)
Business Focus: Bio Therapeutic Drugs
Insider Filings
Latest 10 SEC Form 4 filings for GMAB*US within the last 6 months
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Company News
Apr 03, 2024 01:35 ET
Genmab to Broaden and Strengthen Oncology Portfolio with Acquisition of ProfoundBio
Genmab A/S (Nasdaq: GMAB) and ProfoundBio, Inc. announced today that the companies have entered into a definitive agreement for Genmab to acquire ProfoundBio in an all-cash transaction. ProfoundBio is a privately-owned clinical-stage biotechnology company developing next-generation ADCs and ADC technologies for the treatment of certai
Feb 27, 2024 07:45 ET
U.S. FDA Accepts for Priority Review the Supplemental Biologics License Application for Epcoritamab (EPKINLY®) for Difficult-to-Treat Relapsed or Refractory Follicular Lymphoma
Genmab A/S (Nasdaq: GMAB) and AbbVie (NYSE: ABBV) today announced the U.S. Food and Drug Administration (FDA) granted Priority Review for the supplemental Biologics License Application (sBLA) for epcoritamab-bysp, a T-cell engaging bispecific antibody administered subcutaneously, for the treatment of adult patients with relapsed or refractory (
Valuation Ratios
Industry
Sector
Beta
0.94
--
--
Price to Sales - TTM
8.01
5.54
2.99
Price to Book - most recent quarter
4.12
2.23
2.07
Price to Cash Flow per share - TTM
--
17.45
13.35
Price to Free Cash Flow per share - TTM
18.85
17.11
23.23
Business Summary
| Sector: Healthcare | Industry: Biotechnology & Medical Research |
Genmab A/S is a Denmark-based international biotechnology company. It specializes in the creation and development of antibody therapeutics for the treatment of cancer. The Company is the creator of the approved antibodies: DARZALEX (daratumumab) for the treatment of certain multiple myeloma indications, Kesimpta for the treatment of adults with relapsing forms of multiple sclerosis, TEPEZZA (teprotumumab) for the treatment of thyroid eye disease and FASPRO, for the treatment of adult patients with certain multiple myeloma indications. The first approved Genmab created therapy Arzerra, approved for the treatment of certain chronic lymphocytic leukemia indications, is available in Japan and is also available in other territories via compassionate use or oncology access programs. Genmab develops a broad clinical and pre-clinical product pipeline, and owns four antibody technologies, DuoBody bispecific platform, HexaBody platform, DuoHexaBody platform & HexElect platform.
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