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[Opinion] TREMFYA receives positive CHMP opinion for treatment of patients with Crohn's

Summary by European Pharmaceutical Manufacturer
Johnson & Johnson has announced that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has recommended expanding the Marketing Authorisation for TREMFYA (guselkumab).
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European Pharmaceutical Manufacturer broke the news in on Monday, March 31, 2025.
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