Positive Interactions With EMA Provide Route to Conditional Marketing Authorization of Lead Candidate Nefecon

STOCKHOLM, Oct. 1, 2019 /PRNewswire/ — Calliditas Therapeutics AB (publ) (“Calliditas”) today announced that the European Medicines Agency (EMA) has provided positive guidance related to a conditional marketing authorization (CMA) of the company’s lead compound Nefecon, currently in…

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