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Janssen-Cilag seeks European approval for guselkumab in ulcerative colitis and Crohn's disease treatment

Janssen-Cilag International NV, a Johnson & Johnson company, today announced it has submitted applications to the European Medicines Agency (EMA) seeking to expand the Marketing Authorization Application for TREMFYA® (guselkumab) to include the treatment of adult patients with moderately to severely active ulcerative colitis and moderately to severely active Crohn’s disease. ....

David Lee , European Medicines Agency , Drug Administration , European Union , Janssen Cilag International , Marketing Authorization Application , Ludovic De Beaucoudrey , Senior Director , Therapeutic Area Lead , Janssen Cilag Limited , Global Therapeutic Area Head Immunology , Johnson Innovative , Disease Week Annual Meeting , United European Gastroenterology Week , Biologics License Application , Crohns Disease , Ulcerative Colitis ,

Mental health – from research to remission

Mental health – from research to remission
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Tamara Werner Kiechle , European Year Of Mental Health , European Commission , European Union , European Economic , Social Committee , European Year , Mental Health , Therapeutic Area Lead , Pulmonary Hypertension ,