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Boris Govt to Ban Unvaccinated from Premier League Matches: Report

Boris Govt to Ban Unvaccinated from Premier League Matches: Report
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Stakeholders split over EU food promotional funding for meat, exports

Stakeholders split over EU food promotional funding for meat, exports
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RAX ( Rax Cloud )

RAX ( Rax Cloud )
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Advicenne Receives MHRA Approval to Market Sibnayal (ADV7103) in the UK for the Treatment of dRTA

(1) Regulatory News: Advicenne (Euronext: ADVIC), a specialty pharmaceutical company dedicated to developing and commercializing innovative treatments for those suffering from rare renal diseases, is pleased to announce that the Medicines Healthcare products Regulatory Agency (MHRA) has today granted marketing authorisation for Sibnayal (ADV7103) in the UK, for the treatment of distal renal tubular acidosis (dRTA). With this authorization, and following the recent approval by the European Commission to market Sibnayal for the treatment of dRTA in the European Union, Advicenne is now able to bring to market in the EU and the UK the first and only label-approved drug for the treatment of dRTA in adults, adolescents and children aged one year and older. Advicenne now has the opportunity to make a significant difference to patients suffering from dRTA, classified as an orphan condition in Europe.

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Advicenne Receives MHRA Approval to Market Sibnayal™

Advicenne Receives MHRA Approval to Market Sibnayal™ (ADV7103) in the UK for the Treatment of dRTA July 02, 2021 01:00 ET | Source: Advicenne Advicenne A                                                                                                    Paris, France, 2 nd July 2021 – 7 am CEST – Advicenne (Euronext: ADVIC), a specialty pharmaceutical company dedicated to developing and commercializing innovative treatments for those suffering from rare renal diseases, is pleased to announce that the Medicines & Healthcare products Regulatory Agency (MHRA) has today granted marketing authorisation for Sibnayal™ (ADV7103) in the UK, for the treatment of distal renal tubular acidosis (dRTA). With this authorization, and following the recent approval by the European Commission to market Sibnayal™ for the treatment of dRTA in the European Union

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