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Medicure Receives US FDA Fast Track Designation for MC-1 for PNPO Deficiency

Medicure Receives US FDA Fast Track Designation for MC-1 for PNPO Deficiency
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Washington , United-states , Puerto-rico , Australia , Canada , North-carolina , Canadian , Albertd-friesen , Venture-exchange , Regulation-services-provider , Marley-drug-inc

Tama Potaka | Minister of Māori Development

Tama Potaka | Minister of Māori Development
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Validating A Better ALS Biomarker With Coya's Fred Grossman

Validating A Better ALS Biomarker With Coya's Fred Grossman
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Canada , Fred-grossman , Stanley-appel , Stanleyh-appel-department-of-neurology , Coya-therapeutics , Houston-methodist , Methodist-registry , Critical-path-innovation-meeting , Biomarker-qualification-plan , Fast-track , Relyvrio-phase

Altenar and Fast Track strategic partnership to revolutionise player engagement

Leading sportsbook will deliver targeted campaigns and personalised player journeys.

Charlie-williams , Simon-lidz , Fast-track , Altenar-gaming-platform ,

TME Pharma Announces 33% of Patients Receiving NOX-A12 in Combination With Bevacizumab and Radiotherapy Achieve Two‑Year Survival in GLORIA Phase 1/2 Trial in Brain Cancer

Two of six patients receiving NOX-A12 in combination with bevacizumab and radiotherapy exceeded 24-month survival since the start of therapy



This survival compares favorably to the 5% survival...

Paris , France-general- , France , United-states , Spain , Pharmanv-euronext , Aram-mangasarian , Merck-keytruda , Drug-administration , Twitter , Merck-sharp-dohme-corp , Regulatory-news

TME Pharma N.V.: TME Pharma Announces 33% of Patients Receiving NOX-A12 in Combination With Bevacizumab and Radiotherapy Achieve Two-Year Survival in GLORIA Phase 1/2 Trial in Brain Cancer

TME Pharma N.V.: TME Pharma Announces 33% of Patients Receiving NOX-A12 in Combination With Bevacizumab and Radiotherapy Achieve Two-Year Survival in GLORIA Phase 1/2 Trial in Brain Cancer
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Revive Therapeutics Announces Type C Meeting Request Granted by FDA for Clinical Study of Bucillamine to Treat Long COVID

Revive Therapeutics Announces Type C Meeting Request Granted by FDA for Clinical Study of Bucillamine to Treat Long COVID
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Edgewise Receives European Medicines Agency (EMA) Orphan Drug Designations for Sevasemten (EDG-5506) for the Treatment of Becker and Duchenne Muscular Dystrophies

Edgewise Therapeutics, Inc., , a leading muscle disease biopharmaceutical company, today announced that the European Medicines Agency has granted Orphan Drug Designations for sevasemten for the...

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