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Immunic Presents Data From Phase 2 CALDOSE-1 Trial of Vidofludimus Calcium in Ulcerative Colitis at the United European Gastroenterology Week 2023

NEW YORK, Oct. 16, 2023 /PRNewswire/ Immunic, Inc. , a biotechnology company developing a clinical pipeline of orally administered, small molecule therapies for chronic inflammatory and.

Noord hollandEdna kaplanGeertr dhaensJessica breuPaula schwartzAmsterdam university medical centersExchange commissionRx communications groupImmunic incUnited european gastroenterology weekFull professorGastroenterology endocrinology metabolismVidofludimus calciumPatients with moderatelySeverely active ulcerative colitisResults from

EQS-News: Immunic, Inc : Immunic Presents Data From Phase 2 CALDOSE-1 Trial of Vidofludimus Calcium in Ulcerative Colitis at the United European Gastroenterology Week 2023

EQS-News: Immunic, Inc : Immunic Presents Data From Phase 2 CALDOSE-1 Trial of Vidofludimus Calcium in Ulcerative Colitis at the United European Gastroenterology Week 2023
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Noord hollandGeertr dhaensIndiens wirtschaftEdna kaplanIhre chancenJessica breuPaula schwartzRx communications groupDistribution servicesExchange commissionImmunic incAmsterdam university medical centersPresents data from phaseVidofludimus calciumUlcerative colitisUnited european gastroenterology week

Immunic (IMUX) Presents Data From Phase 2 CALDOSE-1 Trial of Vidofludimus Calcium

Immunic (IMUX) Presents Data From Phase 2 CALDOSE-1 Trial of Vidofludimus Calcium
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Noord hollandGeertr dhaensImmunic incAmsterdam university medical centersUnited european gastroenterology weekFull professorGastroenterology endocrinology metabolismVidofludimus calciumPatients with moderatelySeverely active ulcerative colitisResults fromProspective placebo controlled phaseAbstract session

TREMFYA® (guselkumab) Maintains Key Efficacy Endpoints Through Three Years for Adults with Moderately to Severely Active Crohn s Disease in a Phase 2 Study

TREMFYA® (guselkumab) Maintains Key Efficacy Endpoints Through Three Years for Adults with Moderately to Severely Active Crohn s Disease in a Phase 2 Study
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United statesUniversity of cincinnatiSpring houseBritish columbiaCraig stoltzJan wehkampAnita afzaliJanssen scientific affairsJanssen research developmentCrohn colitis foundationNeither janssen research developmentDivision of digestive diseasesExchange commissionUniversity of cincinnati college medicinePrnewswire janssen pharmaceuticals incJanssen pharmaceutical companies of johnson

FDA Approves Etrasimod for Moderately to Severely Active Ulcerative Colitis

The approval of oral, once-daily etrasimod 2 mg was based on positive data from the phase 3 ELEVATE UC 52 and ELEVATE UC 12 trials.

Michael chioreanEuropean medicines agencyCenter at swedish medicalDrug administrationSwedish medicalMarketing authorization applicationSeverely active ulcerative colitisVersus placeboInduction therapyEtrasimod velsipityUlcerative colitis