Drug

Bimatoprost

As of the edition of 20 October 2026, Bimatoprost is a small molecule: marketed, first approved in 2001 (US); acts on PTGFR; US protection ends in 2031.

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

The drug

Status
Marketed; latest approval 2020
Kind
Small molecule
Brand name
Lumigan
First approved
16 March 2001 (US)
Approvals on record
20 in 8 regions
Holder of the most recent approval
Thea Pharma; 7 holders in all
Registered trials
108, 6 stopped early
Disease areas
Eye; Skin and connective tissue; Immune system; Inherited and neonatal; Hormones; Cancer

US protection

US protection ends in 2031.

The last listed US drug-substance patent ends in 2031. The application that gives this date is held by AbbVie.

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.

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Companies that need a new molecule because of this drug

3 companies on route B because of this drug.

Companies on route B for this drug

In the product

3 companies are on route B because of Bimatoprost.

Target

GeneProteinUniProt
PTGFRProstaglandin F2-alpha receptorP43088

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated201611
Phase 18511
Phase 2191610
Phase 3282512
Phase 4332712
All trials108

Who has held its approvals

CompanyRoleYears
AbbVieOriginator, Applicant and Lead sponsor of trials2001 to now
Senju PharmaceuticalApplicant2009 to now
Thea PharmaApplicant2023 to now