Skip to content

Laquinimod

DRUG15 trials

Sponsors

Teva Branded Pharmaceutical Products R&D, Inc., Teva Pharmaceutical Industries, Ltd., Active Biotech AB, Teva Pharmaceutical Industries, Ltd

Conditions

Crohn's DiseaseEye DiseasesHuntington's DiseaseHuntington's Disease and Multiple ScleroseLupus ArthritisLupus NephritisMultiple SclerosisPharmacodynamics

Phase 1

Phase 2

Laquinimod Phase IIa Study in Active Crohn's Disease
CompletedNCT00737932
Teva Branded Pharmaceutical Products R&D, Inc.Crohn's Disease
Start: 2010-05-31End: 2011-12-31Updated: 2015-03-20
An Extension Study of LAQ/5062 Exploring the Long Term Safety, Tolerability and Clinical Effect Parameters During the Disease
TerminatedNCT00745615
Teva Pharmaceutical Industries, Ltd.Relapsing Remitting Multiple Sclerosis
Start: 2005-12-07End: 2017-07-23Updated: 2019-03-27
A Study of Laquinimod in Participants With Systemic Lupus Erythematosus (SLE) Active Lupus Nephritis
CompletedNCT01085097
Teva Branded Pharmaceutical Products R&D, Inc.Lupus Nephritis
Start: 2010-09-01End: 2012-10-24Updated: 2022-03-09
A Study of Laquinimod in Participants With Systemic Lupus Erythematosus (SLE) Active Lupus Arthritis
CompletedNCT01085084
Teva Branded Pharmaceutical Products R&D, Inc.Lupus Arthritis
Start: 2010-10-04End: 2012-11-12Updated: 2022-07-07
A Clinical Study in Participants With Huntington's Disease (HD) to Assess Efficacy and Safety of Three Oral Doses of Laquinimod
CompletedNCT02215616
Teva Branded Pharmaceutical Products R&D, Inc.Huntington's Disease
Start: 2014-10-28End: 2018-06-19Updated: 2020-05-04
A Phase 2 Clinical Study in Subjects With Primary Progressive Multiple Sclerosis to Assess the Efficacy, Safety and Tolerability of Two Oral Doses of Laquinimod Either of 0.6 mg/Day or 1.5mg/Day (Experimental Drug) as Compared to Placebo
CompletedNCT02284568
Teva Branded Pharmaceutical Products R&D, Inc.Primary Progressive Multiple Sclerosis
Start: 2015-01-12End: 2017-10-01Updated: 2022-03-10

Phase 3

Safety and Efficacy of Orally Administered Laquinimod Versus Placebo for Treatment of Relapsing Remitting Multiple Sclerosis (RRMS)
CompletedNCT00509145
Teva Branded Pharmaceutical Products R&D, Inc.Multiple Sclerosis
Start: 2007-11-13End: 2010-11-08Updated: 2021-11-02
BRAVO Study: Laquinimod Double-blind Placebo-controlled Study in Participants With Relapsing-Remitting Multiple Sclerosis (RRMS) With a Rater Blinded Reference Arm of Interferon β-1a (Avonex®)
CompletedNCT00605215
Teva Branded Pharmaceutical Products R&D, Inc.Multiple Sclerosis
Start: 2008-04-24End: 2011-06-10Updated: 2022-04-21
A Study To Evaluate the Long-Term Safety, Tolerability and Effect on Disease Course
TerminatedNCT00988052
Teva Branded Pharmaceutical Products R&D, Inc.Relapsing Multiple Sclerosis
Start: 2009-11-10End: 2017-07-01Updated: 2021-12-09
A Study to Evaluate the Long-term Safety, Tolerability and Effect of Daily Oral Laquinimod 0.6 mg on Disease Course in Subjects With Relapsing Multiple Sclerosis
TerminatedNCT01047319
Teva Branded Pharmaceutical Products R&D, Inc.Relapsing Multiple Sclerosis
Start: 2010-05-27End: 2017-06-30Updated: 2021-12-09
The Efficacy, Safety, and Tolerability of Laquinimod in Participants With Relapsing Remitting Multiple Sclerosis (RRMS)
CompletedNCT01707992
Teva Branded Pharmaceutical Products R&D, Inc.Multiple Sclerosis
Start: 2013-02-20End: 2017-07-04Updated: 2021-11-09
A Study to Evaluate 2 Doses Of Oral Administration Of Laquinimod Compared to Interferon ß-1a Administered by Injection in Participants With Relapsing Remitting Multiple Sclerosis (RRMS)
WithdrawnNCT01975298
Teva Branded Pharmaceutical Products R&D, Inc.Relapsing Remitting Multiple Sclerosis
Start: 2014-01-31End: 2014-03-31Updated: 2021-11-09

Unknown Phase

Related Papers

Journal of Huntington s Disease2018-06-0131 citations