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US to require patient data for payment of Leqembi, similar Alzheimer s drugs

The U.S. Medicare health plan said on Thursday it would limit reimbursement for Eisai Co Ltd and Biogen Inc s Alzheimer s drug Leqembi to patients whose doctors participate in a health agency database. | June 1, 2023

United statesMark mcclellanMyles minterWilliam blairEli lillyManas mishraEisai co ltdDrug administrationMedicaid servicesDuke universityBiogen inc alzheimerCenters for medicareBiogen incBill berkrotEli lilly and company stock exchangePress release

Health News Roundup: Bayer s pharma chief hopes EU takes time to improve drug rules reform; US FDA proposes higher bar for accelerated approvals for cancer drugs and more

Researchers investigated the impact of antibiotic use on survival in more than 2,100 patients in a hospital in Norway between 2017 and 2021 and found that giving antibiotics to people with common respiratory infections was unlikely to lower the risk of death within 30 days. US FDA seeks to allow salt substitutes in everyday foods The U.S. Food and Drug Administration (FDA) on Friday said it was proposing a rule to allow the use of salt substitutes in everyday foods including cheese, frozen peas and canned tuna, in a bid to cut Americans' salt consumption.

United kingdomUnited statesStefan oelrichBiogen inc alzheimerEuropean commissionPharming groupDrug administrationEuropean unionBiogen incFriday bayer

Health: US FDA proposes higher bar for accelerated approvals for cancer drugs

Health: US FDA proposes higher bar for accelerated approvals for cancer drugs
gdnonline.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from gdnonline.com Daily Mail and Mail on Sunday newspapers.

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US FDA proposes more rigorous trials for accelerated nod of cancer therapy

(Reuters) -The U.S. health regulator on Friday proposed cancer drug developers in most cases conduct more rigorous trials to seek accelerated approval for .

Maju samuelSriraj kalluvilaLeroy leoMerck keytrudaBiogen inc alzheimerDrug administrationBiogen inc

U S FDA approves Reata s rare genetic disorder drug

By Mariam ESunny and Raghav Mahobe (Reuters) -The U.S. Food and Drug Administration on Tuesday approved Reata Pharmaceuticals Inc's drug for the treat.

United statesSherry jacob phillipsRaghav mahobeMariam esunnyMaury raycroftPratik jainKrishna chandra eluriBilly dunnDrug administration onBiogen inc alzheimerReata pharmaceuticals incDrug administrationBiogen incMariame sunny

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