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Data from the PRECISION study of aprocitentan to be presented at the European Society of Hypertension Annual Meeting 2024

Data from the PRECISION study of aprocitentan to be presented at the European Society of Hypertension Annual Meeting 2024
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Switzerland generalUnited statesKrzysztof narkiewiczMarkus schlaichAndrewc weissConvention hallCommittee for medicinal products human useIdorsia pharmaceuticals ltdEuropean society of cardiologySwiss exchangeUniversity of gdanskEuropean society of hypertensionIdorsia ltdHead of the department hypertensionAmerican heart associationHead of investor relations corporate communications

Idorsia Pharmaceuticals Ltd: Data from the PRECISION study of aprocitentan to be presented at the European Society of Hypertension Annual Meeting 2024

Allschwil, Switzerland - May 31, 2024 Idorsia Ltd (SIX: IDIA) today announced that data from the Phase 3 study of aprocitentan, Idorsia's endothelin receptor antagonist, will be presented by Prof.

United statesSwitzerland generalMarkus schlaichAndrewc weissKrzysztof narkiewiczUniversity of gdanskIdorsia pharmaceuticals ltdIdorsia ltdHead of investor relations corporate communicationsAmerican heart associationEuropean society of hypertensionHead of the department hypertensionSwiss exchangeEuropean society of cardiologyEuropean commissionCommittee for medicinal products human use

Update on FDA Priority Review of Dupixent® (dupilumab) for the Treatment of COPD Patients with Type 2 Inflammation

TARRYTOWN, N.Y. and PARIS, May 31, 2024 Regeneron Pharmaceuticals, Inc. and Sanofi today announced the U.S. Food and Drug Administration has extended by three months the target action date of.

United statesFrance generalNathalie phamSandrine guendoulEvan berlandHannah kwaghTimothy gilbertGeorged yancopoulosRegeneron velocimmuneArnaud delepineTarik elgoutniVesna tosicCorentine driancourtEva schaefer jansenFelix lauscherRegeneron genetics center

Regeneron: FDA Extends Review Period For Dupixent As COPD Treatment By Three Month

PARIS (dpa-AFX) - The U.S. Food and Drug Administration has extended by three months the target action date of its priority review of the supplemental Biologics License Application or sBLA for

France generalEuropean medicines agencyCommittee for medicinal products human useMore such health newsRegeneron pharmaceuticals incEuropean unionDrug administrationBiologics license applicationMedicinal productsHuman useIhr portfolio

AbbVie Receives Positive CHMP Opinion for Risankizumab (SKYRIZI®) for the Treatment of Adults with Moderately to Severely Active Ulcerative Colitis

AbbVie Receives Positive CHMP Opinion for Risankizumab (SKYRIZI®) for the Treatment of Adults with Moderately to Severely Active Ulcerative Colitis
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United statesKori wallaceVan asscheEdouard louisGastroenterol hepatolExchange commissionUniversity hospitalNational institute of diabetesBoehringer ingelheimAssociation between disease activityEuropean medicines agencyEuropean commissionCommittee for medicinal products human useDrug administrationEuropean unionCrohn colitis foundation of america