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Year in Review: Age-Related Macular Degeneration

Looking back at some of the year's headline-making news in AMD

United statesNorth carolinaUnited kingdomDuke university medical centerCity ofTufts medical centerAmr dessoukiSanta barbaraIveric bioAstellas pharmaJoseph mellorRahul khuranaArshad khananiApellis pharmaAndre witkinRobert avery

Outcomes Following Brexucabtagene Autoleucel Administered as an FDA-Approved Therapy for Adults with Relapsed/Refractory B-ALL

Outcomes Following Brexucabtagene Autoleucel Administered as an FDA-Approved Therapy for Adults with Relapsed/Refractory B-ALL
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Greg roloffApproved therapy

NSAIDs for Knee Osteoarthritis May Worsen Pain Over Time

Researchers find no long-term benefit and worse inflammation and cartilage quality over 4 years.

United statesNorth carolinaUniversity of texasSan franciscoJohanna luitjensAmandae nelsonUna makrisUniversity of californiaDivision of rheumatologyDepartment of radiologyOsteoarthritis initiativeDivision of rheumatic diseasesRadiological society of north americanRadiological society of north americaRadiological societyNorth america

Adhoc: Relief Therapeutics Holding SA: Relief Reports that its U S Collaboration Partner has Announced that the FDA has Declined Emergency Use Authorization for Aviptadil for a Subgroup of Patients with Critical COVID-19 at Immediate Risk

Relief Therapeutics Holding SA / Key word(s): Regulatory Approval Relief Reports that its U.S. Collaboration Partner has Announced that the FDA has Declined Emergency Use Authorization for Aviptadil

Switzerland generalMichael millerJack weinsteinJonathan javittAdvita lifescience gmbRelief therapeutics holding sa keyPharma researchDrug administrationSwiss exchangeNrx pharmaceuticals incRx communications groupExchange commissionRelief therapeutics holdingNews serviceNeurorx incDeclined emergency use authorization

Relief Reports that its U S Collaboration Partner has Announced that the FDA has Declined Emergency Use Authorization for Aviptadil for a Subgroup of Patients with Critical COVID-19 at Immediate Risk

Relief Therapeutics Holding SA / Key word(s): Regulatory Approval Relief Reports that its U.S. Collaboration Partner has Announced that the FDA has Declined Emergency Use Authorization for Aviptadil for a Subgroup of Patients with Critical COVID-19 at Immediate Risk 04-Jul-2022 / 07:00 CET/CEST .

Switzerland generalMichael millerJack weinsteinJonathan javittAdvita lifescience gmbRelief therapeutics holding sa keyPharma researchDrug administrationSwiss exchangeNrx pharmaceuticals incRx communications groupExchange commissionRelief therapeutics holdingNews serviceNeurorx incDeclined emergency use authorization

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