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    "As a company, Eisai continues to work to address the healthcare challenges faced by underserved populations, which encompasses race, rural location and age." Holman noted that Eisai “selected sites and investigators working within ethnically diverse communities and implemented local outreach activities” for its Phase 3 Leqembi trial.
    A new study points to potential racial and economic disparities in patients’ ability to access Biogen and Eisai's new Alzheimer's disease drug. The medicine, sold under the brand name Leqembi, received full U.S. Food and Drug Administration approval in July 2023, about six months after it won conditional approval.
    Biogen and Eisai share profits and losses equally for Leqembi. The researchers noted limitations to the overall study, including that the analysis only considered first-time prescriptions, and that prescriptions describe when a person has a claim, administration or prescription for the drug, even if they only had evidence of one of these.
    Holman noted that Eisai “selected sites and investigators working within ethnically diverse communities and implemented local outreach activities” for its Phase 3 Leqembi trial. The trial population ultimately had 22.5% of participants who were Hispanic and 4.5% who were Black.
  2. FDA Approves LEQEMBI™ (lecanemab-irmb) Under the ... - Eisai …

  3. New Alzheimer’s drug Leqembi is granted full FDA approval - NBC …

  4. News Release:2021 | Eisai Co., Ltd.

  5. EISAI PRESENTS FULL RESULTS OF LECANEMAB PHASE …

    WEBNov 30, 2022 · Eisai will discuss the results of Clarity AD study with regulatory authorities in the U.S., Japan and Europe with the aim to file for traditional approval in the U.S. and for marketing authorization …

  6. LECANEMAB CONFIRMATORY PHASE 3 CLARITY AD STUDY MET

  7. Eisai’s Alzheimer’s Drug Wins Approval in Japan, Following US

  8. Eisai Alzheimer Drug Shows Promise in Injected-At-Home Form

  9. Eisai, Biogen get U.S. FDA approval for Alzheimer's drug, apply for ...