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ofatumumab

The Scottish Medicines Consortium recommends Novartis’ Kesimpta (ofatumumab) for patients living with relapsing remitting multiple sclerosis (RRMS)

Novartis Kesimpta Ofatumumab

Novartis today announced that eligible patients in Scotland will soon have access to Kesimpta® (ofatumumab), the first self-administered, targeted B-cell therapy for patients with relapsing remitting multiple sclerosis (RRMS) with active disease defined b

July 14, 2021 by firstwordpharma

Novartis bags EU, UK licences for MS therapy Kesimpta

Novartis EU ofatumumab Kesimpta multiple sclerosis

Novartis has received green lights from both the European Commission and the UK's Medicines and Healthcare products Regulatory Agency (MHRA) to market its multiple sclerosis (MS) therapy Kesimpta (ofatumumab).

April 9, 2021 by pharmatimes

Novartis Announces Update on FDA Review of Ofatumumab

Novartis FDA Ofatumumab

Novartis has received notice from the US Food and Drug Administration (FDA) the agency has extended its review of the Supplemental Biologics License Application (sBLA) for ofatumumab (OMB 157) ...

June 15, 2020 by americanpharmaceuticalreview

Regulators expand review time for Novartis' MS drug

Novartis MS ofatumumab CLL

US regulators are extending the review time for Novartis' MS therapy ofatumumab.

June 5, 2020 by pharmatimes

Novartis Announces New Ofatumumab Data at EAN

Novartis ofatumumab teriflunomide EAN

Novartis announced new ofatumumab data from the Phase III ASCLEPIOS trials and the Phase II APLIOS trial were presented virtually at the 6th Congress of the European Academy of Neurology (EAN).

June 3, 2020 by americanpharmaceuticalreview

FDA and EMA accept licence applications for multiple sclerosis treatment

FDA EMA RMS ofatumumab MS

The FDA and EMA have accepted licence applications for ofatumumab, a novel B-cell therapy for patients with relapsing forms of multiple sclerosis (RMS).

March 4, 2020 by europeanpharmaceuticalreview

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