Genmab (Hold, TP: DKK2455.00) - Kesimpta finally gets US approval
Last night the FDA approved subcutaneous ofatumumab (Kesimpta) for the treatment of relapsing forms of multiple sclerosis. In addition, Novartis also announced its intention to pull Arzerra from the US market, paying Genmab a lump sum of USD30m for lost royalties. Genmab has upgraded its guidance accordingly. We reiterate our HOLD, but have lifted our target price to DKK2,455 (2,450) to reflect the Kesimpta approval.Genmab is a biotechnology company specializing in the creation and development of differentiated human antibody therapeutics focused on the treatment of cancer. Co.'s product pipeline includes one marketed product, Arzerra, daratumumab in late stage clinical development, four antibodies in clinical development, and over 20 in-house and partnered pre-clinical programs. Co.'s Arzerra (ofatumumab) is a human monoclonal antibody which targets an epitope on the CD20 molecule. Co.'s proprietary technologies include the DuoBody technology, which creates antibodies that can target two molecules at once, and the HexaBody technology, which allows for the creation of more potent antibodies.
DNB Markets is the investment banking arm of DNB Bank ASA and is focused primarily on the Nordic region, as well as internationally on niches such as global shipping, energy and related services, and seafood. DNB Markets offers services in FICC, Equities and Investment Banking advisory from offices in Oslo, Stockholm, London, Singapore and New York. Equity research coverage is offered on c250 Nordic companies. DNB was ranked no.2 in Extel Nordic Research 2017. The DNB Markets’ Credit and FICC Macro & FX Research teams are repeatedly highly rated by Prospera Nordic Institutional Investor Surveys.
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