Drug

Pergolide

As of the edition of 20 October 2026, Pergolide is a small molecule: withdrawn from the market in 2007; acts on DRD1, DRD2 and DRD3 and 2 more; no US protection is listed.

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

The drug

Status
Withdrawn from market, 2007
Kind
Small molecule
Brand name
Permax
First approved
30 December 1988 (US)
Approvals on record
3 in 1 region
Holder of the most recent approval
Bausch Health
Withdrawn from market
1 January 2007 (in some regions)
Registered trials
9, 1 stopped early
Disease areas
Mental health; Chemically induced; Nervous system; Inherited and neonatal

US protection

No US protection is listed.

The FDA registers list no drug-substance patent or exclusivity that counts for this drug.

This is the US only.

Companies that need a new molecule because of this drug

3 company-target rows on route B and 3 company-target rows on route A because of this drug.

Companies on route B for this drug

In the product

3 company-target rows are on route B because of Pergolide.

Companies on route A for this drug

In the product

3 company-target rows are on route A because of Pergolide.

Targets

GeneProteinUniProt
DRD2Dopamine receptor D2P14416
DRD1Dopamine receptor D1P21728
DRD4Dopamine receptor D4P21917
DRD5Dopamine receptor D5P21918
DRD3Dopamine receptor D3P35462

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated5200
Phase 22200
Phase 31100
Phase 41001
All trials9

Who has held its approvals

CompanyRoleYears
Eli LillyEarlier holder1988 to now
Bausch HealthAcquired holder and Lead sponsor of trials2005 to now