Basel, April 17, 2024 – Novartis today announced data from the ALITHIOS open-label extension study showing sustained efficacy of first-line, continuous Kesimpta ® (ofatumumab) treatment for up to six ...
Kesimpta (ofatumumab) is a prescription drug used to treat certain kinds of multiple sclerosis (MS) and clinically isolated syndrome. Kesimpta’s cost may depend on factors such as your dosage and ...
Kesimpta is a medicine used to treat relapsing forms of multiple sclerosis (MS). Relapsing forms of MS include clinically isolated syndrome, relapsing-remitting MS, and active secondary progressive MS ...
Patients treated with Kesimpta experienced considerable decreases in relapse rates Patients treated with Kesimpta experienced considerable decreases in relapse rates Novartis has presented pivotal ...
Novartis has secured backing from NICE for its relapsing multiple sclerosis (RMS) therapy Kesimpta in the UK, just two weeks after the drug was approved by the national drugs regulator. The ...
Kesimpta (ofatumumab) is a prescription drug used to treat clinically isolated syndrome (CIS) and multiple sclerosis (MS) in adults. The drug comes as a liquid solution for injection under the skin.
(RTTNews) - Novartis AG (NVS) said that an analysis of treatment-naive people who were recently diagnosed with relapsing multiple sclerosis found that first-line use of Kesimpta for up to six years ...
Kesimpta, a CD20-directed cytolytic monoclonal antibody, is the first B-cell therapy intended for patient self-administration. The Food and Drug Administration (FDA) has approved Kesimpta® (ofatumumab ...
ARTIOS Phase IIIb, open-label, single-arm, prospective study showed a substantial reduction in disease activity in people with relapsing multiple sclerosis (RMS) following switch to Kesimpta after ...
EAST HANOVER, N.J., Aug. 20, 2020 /PRNewswire/ -- Novartis today announced that the US Food and Drug Administration (FDA) has approved Kesimpta® (ofatumumab, formerly OMB157) as an injection for ...
Please provide your email address to receive an email when new articles are posted on . 80% of study participants remained free of disability-worsening events at 6 months. Cumulative event rates for 6 ...