More and more people are talking about Genmab A/S over the last few weeks. Is it worth buying the Pharmaceutical stock at a price of $22.79? Only time will tell. The information below will give you a basic idea of what this investment may entail:
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Genmab A/S has moved -21.1% over the last year, and the S&P 500 logged a change of 34.8%
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GMAB has an average analyst rating of buy and is -42.17% away from its mean target price of $39.4 per share
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Its trailing earnings per share (EPS) is $1.24
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Genmab A/S has a trailing 12 month Price to Earnings (P/E) ratio of 18.4 while the S&P 500 average is 29.3
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Its forward earnings per share (EPS) is $1.64 and its forward P/E ratio is 13.9
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The company has a Price to Book (P/B) ratio of 0.05 in contrast to the S&P 500's average ratio of 4.74
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Genmab A/S is part of the Health Care sector, which has an average P/E ratio of 26.07 and an average P/B of 3.53
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GMAB has reported YOY quarterly earnings growth of 7.0% and gross profit margins of 1.0%
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The company has a free cash flow of $5.59 Billion, which refers to the total sum of all its inflows and outflows of cash over the last quarter
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Genmab A/S develops antibody therapeutics for the treatment of cancer and other diseases primarily in Denmark. The company markets DARZALEX, a human monoclonal antibody for the treatment of patients with multiple myeloma (MM); teprotumumab for the treatment of thyroid eye disease; and Amivantamab for advanced or metastatic gastric or esophageal cancer and NSCLC. Its products include daratumumab to treat MM, non-MM blood cancers, and AL amyloidosis; GEN1047; tisotumab vedotin for treating cervical, ovarian, and solid cancers; DuoBody-PD-L1x4-1BB, and DuoBody-CD40x4-1BB for treating solid tumors; Epcoritamab for relapsed/refractory diffuse large B-cell lymphoma and chronic lymphocytic leukemia; and HexaBody-CD38 and GEN3017 for treating hematological malignancies. In addition, the company develops Inclacumab, which is in Phase 3 trial for vaso-occlusive crises; Camidanlumab tesirine to treat hodgkin lymphoma and solid tumors; JNJ-64007957 and JNJ-64407564 to treat MM; PRV-015 for treating celiac disease; Mim8 for treating haemophilia A; and Lu AF82422 for treating multiple system atrophy disease. It operates various active pre-clinical programs. The company has a commercial license and collaboration agreement with Seagen Inc. to co-develop tisotumab vedotin. It also has a collaboration agreement with argenx to discover, develop, and commercialize novel therapeutic antibodies with applications in immunology and oncology; and AbbVie for the development of epcoritamab, as well as collaborations with BioNTech, Janssen, and Novo Nordisk A/S. Genmab A/S was founded in 1999 and is headquartered in Copenhagen, Denmark.