The Japanese Ministry of Health, Labor and Welfare has granted priority review status to the Alzheimer’s disease drug, lecanemab, of Japanese drugmaker Eisai Co Ltd and U.S. biotech firm Biogen Inc.
Once the priority status has been granted, the target total review period is shortened.
Lecanemab was recently granted accelerated approval in the US.
A late-stage study showed the drug reduced the rate of cognitive decline in patients with early Alzheimer’s by 27 percent, compared with a placebo.
Similar experimental medications have largely all failed in the past.
Eisai also requested complete U.S. approval of the medication earlier this month. Food and Drug Administration (FDA) as a treatment for patients with neurodegenerative disease in its early stages.


FDA Fast-Track Drug Reviews Delayed Over Safety and Efficacy Concerns
AstraZeneca’s LATIFY Phase III Trial of Ceralasertib Misses Primary Endpoint in Lung Cancer Study
Panama Supreme Court Voids CK Hutchison Port Concessions, Raising Geopolitical and Trade Concerns
S&P 500 Rises as AI Stocks and Small Caps Rally on Strong Earnings Outlook
JPMorgan Lifts Gold Price Forecast to $6,300 by End-2026 on Strong Central Bank and Investor Demand
China to Add Eli Lilly’s Mounjaro to National Health Insurance in 2025
Elon Musk’s SpaceX Acquires xAI in Historic Deal Uniting Space and Artificial Intelligence
Nvidia Confirms Major OpenAI Investment Amid AI Funding Race
Sam Altman Reaffirms OpenAI’s Long-Term Commitment to NVIDIA Amid Chip Report
Japan’s Agricultural, Forestry and Fishery Exports Hit Record High in 2025 Despite Tariffs
IMF Forecasts Global Inflation Decline as Growth Remains Resilient
Trump Backs Review of U.S. Childhood Vaccine Schedule After Hepatitis B Policy Change
Federal Appeals Court Blocks Trump-Era Hospital Drug Rebate Plan
EU Recovery Fund Faces Bottlenecks Despite Driving Digital and Green Projects 



