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News Vifor Pharma Xetra

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CH0364749348

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European Commission Solicits Feedback on Vifor Pharma's Anticompetition Commitments	19/04	MT
CSL Vifor Announces Topline Results from Two-Year Primary Efficacy Endpoint in Pivotal Phase 3 DUPLEX Study of Sparsentan in Focal Segmental Glomerulosclerosis	02/23/02	CI
Court Cancels Public Shares of Vifor Pharma after Merger with CSL	14/22/14	MT
Cancellation of remaining publicly held registered shares of Vifor Pharma AG	14/22/14	BU
Ferinject® approved in Chinafor the treatment of iron deficiency in adult patients	28/22/28	BU
Iron Deficiency Day 2022: CSL Vifor calls to take iron seriously	25/22/25	BU
Rhythm Biosciences Expands Executive Management Team, Registers Diagnostic Blood Test With New Zealand	03/22/03	MT
Approval of extension of exemptions from SIX disclosure and publicity obligations	20/22/20	BU
Australia's CSL raises annual profit forecast on Swiss acquisition	17/22/17	RE
Global markets live: Darktrace, Intel, Twitter, Meta, Uber...	12/22/12
Vifor Pharma Gets Approval To Delist From Swiss Bourse	12/22/12	MT
Approval of delisting of Vifor Pharma AG's registered shares	12/22/12	BU
Swissmedic OKs ChemoCentryx's Combo Therapy For Rare Blood Vessel Disease	28/22/28	MT
Fitch Pulls Vifor Pharma's Rating After CSL Takeover	25/22/25	MT
Vifor, Travere's Application for Rare Kidney Disease Drug Under Review in EU	23/22/23	MT
CSL Vifor and Travere Therapeutics announce EMA has accepted for review the Conditional Marketing Authorization application for sparsentan for the treatment of IgA Nephropathy	22/22/22	BU
Vifor-Fresenius Medical Care JV Wins US Infringement Case Against Teva	22/22/22	MT
VFMCRP announces U.S. Court upholds validity of Velphoro® patent	22/22/22	BU
Kapruvia® approved in Switzerland with additional regulatory decisions expected in H2 2022	19/22/19	BU
VFMCRP - Tavneos (avacopan) recommended by England's NICE for the treatment of AAV (GPA/MPA)	18/22/18	AQ

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News Vifor Pharma Xetra

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