Leqembi to Cost 2.98 Million Yen per Year, Re-Pricing Might Be Triggered on Patient Upswing

To read the full story

• Sign In
• Subscribe

Related Article

• Leqembi Likely to Face 15% Price Cut Under Special CEA Rule
  July 10, 2025

• Kisunla Gets Reimbursement Listing with Daily NHI Price of 8,560 Yen
  November 14, 2024

• Japan to Apply Leqembi’s General Pricing Rules for Similar AD Therapies
  November 14, 2024

• Kisunla to Follow Same Rules as Leqembi in Pricing and Post-Launch Review
  October 10, 2024

• Is Case of Leqembi a “Steppingstone” to New CEA Price Adjustment Rule? Pharma Industry on Guard
  January 30, 2024

• Eisai CEO Anticipates Leqembi Approval in Europe and China by March
  December 18, 2023

• Leqembi to Debut on Dec. 20; Eisai Sees SC Version and Blood Biomarker as Drivers for Wider Use
  December 14, 2023

• Chuikyo Agrees to Adopt Normal Rules to Price, Re-Price Leqembi
  November 16, 2023

• Industry Prods Careful Debate on Creating Separate Rules for Leqembi Re-Pricing
  November 9, 2023

• Medical, Long-Term Care Data Linkage Holds Key to CEA: Leqembi Debate
  October 30, 2023

• Leqembi’s Initial Pricing Won’t Factor in Benefits in Long-Term Care
  October 19, 2023

• Many Back Expansion in Range of CEA Price Tweaks for Pricey Drugs: Chuikyo
  October 5, 2023

• Post-Launch Re-Pricing Likely the Focus of Chuikyo Leqembi Discussions
  October 5, 2023

• As Chuikyo Begins Pricing Debate of Leqembi, Panelists Urge Safety, Fair Access
  September 28, 2023

• Leqembi Subject to Cost Control Rule for Potential Big Sellers, MHLW Still Set to Meet Listing Deadline
  September 26, 2023

• Japan Approves Eisai/Biogen’s Alzheimer’s Drug Leqembi
  September 25, 2023

• Japan Panel OKs Novartis’ siRNA Dyslipidemia Therapy and More
  August 22, 2023

• Eisai’s Alzheimer’s Drug Clears Advisory Panel, Now in Line for Japan Approval
  August 22, 2023

• Full US Nod in Hand, Eisai CEO Keeps 1 Trillion Yen Sales Target for FY2030
  July 10, 2023

• FDA Awards Full Approval to Eisai’s Alzheimer’s Drug
  July 7, 2023

• FDA Advisors Back Full Approval of Eisai’s Alzheimer’s Med
  June 12, 2023

• Eisai’s Leqembi Wins Coverage from US Veteran’s Body
  March 15, 2023

• FDA Accepts Eisai’s Lecanemab Application for Early July Target
  March 6, 2023

• Lecanemab Earns Priority Review in Japan, Eisai Aims for Approval by Year-End
  January 31, 2023

• Lecanemab Application Accepted for Review in Europe; FY2023 Approval Eyed
  January 30, 2023

• Alzheimer’s Drug Leqembi Now Available in US: Eisai/Biogen
  January 24, 2023

• Alzheimer’s Med Lecanemab Submitted in Japan: Eisai
  January 16, 2023

• Eisai Files Alzheimer’s Med Lecanemab in Europe
  January 12, 2023

• Leqembi Likely to Hit Peak Sales after 2030, US$26,500 Price Matches Value: Eisai CEO
  January 10, 2023

• Lecanemab Nabs Accelerated Approval in US, Set to Hit Market Late January
  January 10, 2023

• Eisai Says 2 Trial Deaths Not Attributed to Lecanemab, No Change in Submission Plan
  December 1, 2022

• Japan Expert Sees Lecanemab Initially Treating Only a Few Tens of Thousands of Patients with Immature Care Setup
  October 12, 2022

• Lecanemab Hits PIII Mark with 27% Cut in Clinical Decline, Eisai Set for Submissions by March-End
  September 29, 2022

• Eisai on Track towards Lecanemab PIII Readout by Sept.-End, Japan/US/EU Filing by March 2023
  August 8, 2022

• Lecanemab Accepted for US Review, Action Date Set for January: Eisai/Biogen
  July 7, 2022

• Eisai Completes Rolling Submission for Lecanemab in US
  May 11, 2022

• Lecanemab Scores Positive Results in PIIb Study: Eisai/Biogen
  March 23, 2022

• Eisai Begins Data Submission for Lecanemab for Swift Approval in Japan
  March 7, 2022

• Eisai’s Lecanemab Bags Fast-Track Status in US
  December 27, 2021

• Eisai/Biogen Begin US Rolling Submission for Alzheimer’s Med Lecanemab
  September 28, 2021

• BAN2401 Gets FDA’s Breakthrough Therapy Tag: Eisai/Biogen
  June 25, 2021