Drug

Quinidine

As of the edition of 20 October 2026, Quinidine is a small molecule: marketed, first approved in 1982 (US); acts on SCN10A, SCN11A and SCN1A and 7 more; no US protection is listed.

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

The drug

Status
Marketed; latest approval 1996
Kind
Small molecule
Brand name
Duraquin
First approved
1 January 1982 (US)
Approvals on record
6 in 2 regions
Holder of the most recent approval
Otsuka; 6 holders in all
Withdrawn from market
15 February 2016 (in some regions)
Registered trials
34, 4 stopped early
Disease areas
Mental health; Nervous system; Heart and blood vessels; Infections; Nutrition and metabolism; Digestive system

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.

Targets

GeneProteinUniProt
SCN1ASodium channel protein type 1 subunit alphaP35498
SCN4ASodium channel protein type 4 subunit alphaP35499
SCN7ASodium channel protein type 7 subunit alphaQ01118
SCN5ASodium channel protein type 5 subunit alphaQ14524
SCN9ASodium channel protein type 9 subunit alphaQ15858
SCN2ASodium channel protein type 2 subunit alphaQ99250
SCN3ASodium channel protein type 3 subunit alphaQ9NY46
SCN11ASodium channel protein type 11 subunit alphaQ9UI33
SCN8ASodium channel protein type 8 subunit alphaQ9UQD0
SCN10ASodium channel protein type 10 subunit alphaQ9Y5Y9

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase 1191801
Phase 26500
Phase 36501
Phase 43102
All trials34

Who has held its approvals

CompanyRoleYears
Eli LillyLater holder and Lead sponsor of trials1989 to now
PfizerAcquired holder, Later holder and Earlier holder2003 to now
BayerAcquired holder2008 to now