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Eli Lilly and Co's Alzheimer's drug, Donanemab, may be rejected by the United Kingdom's healthcare regulatory institutions.
After the regulatory institutions in the United Kingdom refused to approve Leqembi, the Alzheimer's disease drug owned by Baijian, for use in the National Health Service (NHS), there have been reports that Donanemab, another Alzheimer's disease drug owned by Eli Lilly and Co, will face the same fate.
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Eisai and Biogen's Alzheimer's Drug Leqembi Receives MHRA Approval in Great Britain
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Biogen (BIIB.US) and Eisai (ESALF.US) subsidiary's Alzheimer's disease drug Leqembi has received marketing authorization in the United Kingdom.
According to the Zhītōng Finance APP, Biijian (BIIB.US) and its Japanese partner Wèicái (ESALF.US) announced on Thursday that their groundbreaking Alzheimer's disease treatment drug Leqembi (lecanemab) has obtained marketing authorization in the United Kingdom.
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Eisai and Biogen's Alzheimer's Drug Leqembi Receives First European Approval in Great Britain
Express News | Biogen: Eisai Working With Nice, SMC and Nhs to Make This Medicine Available to Eligible People Living With Early Ad as Soon as Possible
Express News | UK's Nice: Benefits of Alzheimer’s Treatment Lecanemab Are Too Small to Justify Cost to the Nhs
Express News | UK's Mhra: Lecanemab Licensed for Adult Patients in Early Stages of Alzheimer’s Disease
Express News | UK's Mhra: Together With Conditions of Licence Approval, Appropriate Regulatory Standards for Lecanemab Have Been Met
Express News | UK's Nice: Issued Draft Guidance for Consultation Not Recommending Lecanemab for Use on Nhs as It Is Not Cost Effective Use of Limited Nhs Funding
Leqembi (Lecanemab) Authorized for Early Alzheimer's Disease in Great Britain
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