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MHRA approves new diagnostic agent for adult patients showing signs of cognitive impairment for Alzheimer’s disease

News Healthcare & Pharma General Updates
Date: 27th Nov, 2024 Source: Medicines and Healthcare products Regulatory Agency (MHRA) Country: United Kingdom Original Source

Brief

"On November 27, 2024, the Medicines and Healthcare products Regulatory Agency (MHRA) approved flortaucipir (Tauvid), a radiopharmaceutical product for adults with memory problems. This approval enables doctors to perform PET scans to determine if patients have abnormal forms of tau protein in their brain, which is associated with Alzheimer's disease."

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Medicines and Healthcare products Regulatory Agency (MHRA)

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