FDA and EMA accept Novartis’ filings for MS drug Siponimod

07:37 EDT 9 Oct 2018 | Pharmaceutical Business Review

The regulators have accepted the firm’s filings for investigational oral and once-daily siponimod to treat secondary progressive multiple sclerosis (SPMS) in adults. Siponimod is an investigational and selective

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Original Article: FDA and EMA accept Novartis’ filings for MS drug Siponimod

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