Drug

Eribulin

As of the edition of 20 October 2026, Eribulin is a small molecule: marketed, first approved in 2010 (US); acts on TUBB, TUBB1 and TUBB2A and 6 more; US protection ended in 2026.

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

The drug

Status
Marketed; latest approval 2011
Kind
Small molecule
Brand name
Halaven
First approved
15 November 2010 (US)
Approvals on record
6 in 4 regions
Holder of the most recent approval
Baxter Healthcare; 2 holders in all
Registered trials
173, 25 stopped early
Disease areas
Cancer; Skin and connective tissue; Urinary and reproductive; Pregnancy and women's health; Hormones; Lungs and airways

US protection

US protection ended in 2026.

The last listed US exclusivity ended in 2026. The application that gives this date is held by Eisai.

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

9 company-target rows on route B because of this drug.

Companies on route B for this drug

In the product

9 company-target rows are on route B because of Eribulin.

Targets

GeneProteinUniProt
TUBB4ATubulin beta-4A chainP04350
TUBBTubulin beta chainP07437
TUBB4BTubulin beta-4B chainP68371
TUBB3Tubulin beta-3 chainQ13509
TUBB2ATubulin beta-2A chainQ13885
TUBB8Tubulin beta-8 chainQ3ZCM7
TUBB6Tubulin beta-6 chainQ9BUF5
TUBB2BTubulin beta-2B chainQ9BVA1
TUBB1Tubulin beta-1 chainQ9H4B7

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated11601
Phase 1332147
Phase 2108522415
Phase 317762
Phase 44300
All trials173

Who has held its approvals

CompanyRoleYears
EisaiOriginator and Lead sponsor of trials2003 to now
Baxter HealthcareApplicant2025 to now