Drug

Pimavanserin

As of the edition of 20 October 2026, Pimavanserin is a small molecule: marketed, first approved in 2016 (US); acts on HTR2A; US protection ends in 2030.

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

The drug

Status
Marketed; latest approval 2016
Kind
Small molecule
Brand name
Nuplazid
First approved
29 April 2016 (US)
Approvals on record
3 in 1 region
Holder of the most recent approval
Acadia Pharmaceuticals
Registered trials
41, 8 stopped early
Disease areas
Nervous system; Mental health; Eye; Heart and blood vessels; Inherited and neonatal

US protection

US protection ends in 2030.

The last listed US drug-substance patent ends in 2030. The application that gives this date is held by Acadia Pharmaceuticals.

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

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

See the exact date and the 12 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 Pimavanserin.

Target

GeneProteinUniProt
HTR2A5-hydroxytryptamine receptor 2AP28223

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated2010
Phase 13201
Phase 2171043
Phase 3151203
Phase 44211
All trials41

Who has held its approvals

CompanyRoleYears
Acadia PharmaceuticalsOriginator and Lead sponsor of trials2016 to now