Drug

Lecanemab

As of the edition of 20 October 2026, Lecanemab is an antibody: marketed, first approved in 2023 (US); acts on APP; US protection ends in 2035.

Sources: FDA Orange Book and Purple Book, other approval registers, ClinicalTrials.gov, ChEMBL.

The drug

Status
Marketed; latest approval 2025
Kind
Antibody
Brand name
Leqembi
First approved
6 January 2023 (US)
Approvals on record
7 in 4 regions
Holder of the most recent approval
Eisai
Registered trials
22, 0 stopped early
Disease areas
Mental health; Nervous system

US protection

US protection ends in 2035.

US protection ends in 2035, computed as 12 years from the first US licence because FDA publishes no date for this product. The application that gives this date is held by Eisai. The date is computed, not published.

This is the US only, and it is not the date generics or biosimilars can enter.

The exact date and the listings behind it

In the product

2 listings count towards this date. The exact date and each listing are in the product.

See the exact date and the 2 listings behind itRequest access. Nothing is shown until you do.

Companies that need a new molecule because of this drug

1 company on route B because of this drug.

Companies on route B for this drug

In the product

1 company is on route B because of Lecanemab.

Target

GeneProteinUniProt
APPAmyloid-beta precursor proteinP05067

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated8080
Phase 14310
Phase 22110
Phase 36060
Phase 42020
All trials22

Who has held its approvals

CompanyRoleYears
EisaiOriginator and Lead sponsor of trials2012 to now