Drug

Vorapaxar

As of the edition of 20 October 2026, Vorapaxar is a small molecule: marketed, first approved in 2014 (US); acts on F2R; US protection ends in 2027.

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

The drug

Status
Marketed; latest approval 2014
Kind
Small molecule
Brand name
Zontivity
First approved
8 May 2014 (US)
Approvals on record
1 in 1 region
Holder of the most recent approval
Merck & Co.
Withdrawn from market
23 June 2017 (in some regions)
Registered trials
12, 1 stopped early
Disease areas
Heart and blood vessels; Nervous system; Hormones; Infections; Nutrition and metabolism

US protection

US protection ends in 2027.

The last listed US drug-substance patent ends in 2027. The application that gives this date is held by Merck & Co..

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

1 listing counts towards this date. The exact date and each listing are in the product.

See the exact date and the 1 listing 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 Vorapaxar.

Target

GeneProteinUniProt
F2RProteinase-activated receptor 1P25116

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase 11100
Phase 24400
Phase 33201
Phase 44400
All trials12

Who has held its approvals

CompanyRoleYears
Merck & Co.Originator and Lead sponsor of trials2005 to now