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Press Releases Vifor Pharma Berne S.E.

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Apr. 19	European Commission Solicits Feedback on Vifor Pharma's Anticompetition Commitments	MT
2023	CSL Vifor Announces Topline Results from Two-Year Primary Efficacy Endpoint in Pivotal Phase 3 DUPLEX Study of Sparsentan in Focal Segmental Glomerulosclerosis	CI

Press Releases

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Cancellation of remaining publicly held registered shares of Vifor Pharma AG	22-12-14	BU
Ferinject® approved in Chinafor the treatment of iron deficiency in adult patients	22-11-28	BU
Iron Deficiency Day 2022: CSL Vifor calls to take iron seriously	22-11-25	BU
Approval of extension of exemptions from SIX disclosure and publicity obligations	22-10-20	BU
Approval of delisting of Vifor Pharma AG's registered shares	22-10-12	BU
CSL Vifor and Travere Therapeutics announce EMA has accepted for review the Conditional Marketing Authorization application for sparsentan for the treatment of IgA Nephropathy	22-08-22	BU
VFMCRP announces U.S. Court upholds validity of Velphoro® patent	22-08-22	BU
Kapruvia® approved in Switzerland with additional regulatory decisions expected in H2 2022	22-08-19	BU
VFMCRP - Tavneos (avacopan) recommended by England's NICE for the treatment of AAV (GPA/MPA)	22-08-18	AQ
Tavneos® (avacopan) recommended by England’s NICE for the treatment of AAV (GPA/MPA)	22-08-18	BU
Finalization of Vifor Pharma acquisition	22-08-02	BU
Vifor Pharma Group - Extension of the postponement of the settlement of Vifor Pharma tender offer	22-07-14	AQ
CSL Limited - Extension of the postponement of the settlement of Vifor Pharma tender offer	22-07-13	AQ
Extension of the postponement of the settlement of Vifor Pharma tender offer	22-07-13	BU
THE EU COMMISSION OPENS ANTITRUST INVESTIGATION INTO COMPETITORS SUSPECTED ILLEGAL DISPARAGEMENT OF PHARMACOSMOS' MAIN INTRAVENOUS IRON PRODUCT	22-06-22	AQ
Update on the timeline for Vifor Pharma tender offer	22-05-12	BU
Kapruvia® approved by European Commission for the treatment of moderate-to-severe pruritus in hemodialysis patients	22-04-28	AQ
94th Vifor Pharma Group Annual General Meeting	22-04-26	BU
DIAMOND trial: Veltassa® enables patients to achieve long-term potassium control and optimized RAASi therapy	22-04-04	BU
Publication of definitive end result for Vifor Pharma tender offer	22-03-28	BU

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