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Johnson & Johnson submits regulatory applications to

Media contact:Sophie DaneauSdaneau@its.jnj.com+33 6 3178 8798Investor contact:Raychel Kruperinvestor-relations@its.jnj.com For European and UK.

United kingdomRegion flamandeDavid leeSophie daneauDrug administrationJapan pharmaceuticalsExchange commissionEuropean unionCanadian agency for drugs technologies in healthJanssen biotech incCrohn colitis foundationNone of janssen research developmentDevices agencyJanssen research developmentEuropean medicines agencyJanssen cilag international

Johnson & Johnson submits supplemental Biologics License Application to U S FDA seeking approval of TREMFYA® (guselkumab) for the treatment of adults with moderately to severely active ulcerative colitis

/PRNewswire/ Johnson & Johnson today announced the submission of a supplemental Biologics License Application (sBLA) to the U.S. Food and Drug.

Spring houseBritish columbiaDavid leeScandj rheumatolPrnewswire johnsonCraig stoltzExchange commissionDevices agencyDrug administrationCanadian agency for drugs technologies in healthEuropean commissionNone of janssen research developmentJapan pharmaceuticalsNational institutes of healthJanssen biotech incCrohn colitis foundation

Johnson & Johnson submits supplemental Biologics License Application to U S FDA seeking approval of TREMFYA® (guselkumab) for the treatment of adults with moderately to severely active ulcerative colitis

Johnson & Johnson submits supplemental Biologics License Application to U S FDA seeking approval of TREMFYA® (guselkumab) for the treatment of adults with moderately to severely active ulcerative colitis
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Spring houseBritish columbiaCraig stoltzScandj rheumatolPrnewswire johnsonDavid leeEuropean commissionJanssen biotech incDrug administrationNone of janssen research developmentExchange commissionCanadian agency for drugs technologies in healthJapan pharmaceuticalsCrohn colitis foundationJanssen research developmentNational institutes of health

TREMFYA® (guselkumab) Provides Sustained Improvements Across All Minimal Disease Activity Domains for Adults Living with Active Psoriatic Arthritis in Phase 3b Trial

TREMFYA® (guselkumab) Provides Sustained Improvements Across All Minimal Disease Activity Domains for Adults Living with Active Psoriatic Arthritis in Phase 3b Trial
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Spring houseUnited statesScandj rheumatolLaura coatesTerence rooneyZismand comorbiditiesJanssen pharmaceutical companies of johnsonJanssen pharmaceutical companiesDevices agencyUniversity of oxfordStanford health assessment questionnaireArthritis foundationJanssen scientific affairsEuropean congressNone of the janssen pharmaceutical companiesJanssen research development

Johnson & Johnson : TREMFYA® (guselkumab) Provides Sustained Improvements Across All Minimal Disease Activity Domains for Adults Living with Active Psoriatic Arthritis in Phase 3b Trial

SPRING HOUSE, PENNSYLVANIA, May 31, 2023 - The Janssen Pharmaceutical Companies of Johnson & Johnson today announced new data from the Phase 3b COSMOS clinical trial showing that treatment. | May 31, 2023

United statesSpring houseZismand comorbiditiesLaura coatesTerence rooneyCraig stoltzScandj rheumatolNational library of medicineStanford health assessment questionnaireCanadian agency for drugs technologies in healthJanssen scientific affairsJanssen pharmaceutical companiesArthritis foundationDevices agencyExchange commissionJanssen pharmaceutical companies of johnson