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Last Updated: September 28, 2020

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CLINICAL TRIALS PROFILE FOR OPICAPONE

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All Clinical Trials for Opicapone

Trial ID Title Status Sponsor Phase Start Date Summary
NCT01227655 Efficacy and Safety of BIA 9-1067 in Idiopathic Parkinson's Disease Patients. Completed Bial - Portela C S.A. Phase 3 2011-03-01 Parkinson's disease (PD) is a neurodegenerative disorder of unknown aetiology with an estimated incidence of 4.5-16/100,000 persons/year. BIA 9-1067 is currently being developed by BIAL (Portela & Cª,S.A.) to be used in addition to L-DOPA (Levodopa) /carbidopa or L-DOPA (Levodopa) / preparations in PD patients. Promising results have been obtained for BIA 9-1067 in previous studies.
NCT01515891 Absorption, Distribution, Metabolism and Excretion of [14C]-Labeled BIA 9-1067 and Metabolites Completed Bial - Portela C S.A. Phase 1 2009-05-01 To determine the absorption, metabolism and excretion of BIA 9-1067.
NCT01851850 Continuation Treatment Protocol for Patient Who Participated in the BIA 9-1067-302 Clinical Trial Unknown status Rabin Medical Center Phase 3 2013-05-01 The purpose of the study is to extend the use of opicapone 25 or 50mg once per day by subjects who participated in the BIA 9-1067-302 clinical trial according form 4a for additional three years.
NCT02101190 Pharmacokinetics of BIA 9-1067 in Subjects With Hepatic Impairment Completed Bial - Portela C S.A. Phase 1 2010-03-01 The purpose of this study is to assess the pharmacokinetics (PK) of BIA 9-1067 in patients with moderate chronic hepatic impairment and in matched healthy subjects.
NCT02170376 The Effect of BIA 9-1067 at Steady-state on the Levodopa Pharmacokinetics Completed Bial - Portela C S.A. Phase 1 2011-09-01 The purpose of this study is to determine the effect of repeated dosing of once-daily 25, 50 and 75 mg opicapone (OPC, development code BIA 9-1067) on the levodopa pharmacokinetics (PK), in comparison to placebo and 200 mg entacapone (ENT).
NCT02305017 Effect of Paracetamol on Opicapone Pharmacokinetics in Healthy Volunteers Completed Bial - Portela C S.A. Phase 1 2014-03-01 Single-centre, open-label, randomised, two-way cross-over study consisting of 2 periods separated by a washout period of 14 days or more.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Opicapone

Condition Name

Condition Name for Opicapone
Intervention Trials
Parkinson Disease 7
Parkinson's Disease 4
Parkinson 1
Epilepsy 1
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Condition MeSH

Condition MeSH for Opicapone
Intervention Trials
Parkinson Disease 13
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Clinical Trial Locations for Opicapone

Trials by Country

Trials by Country for Opicapone
Location Trials
United Kingdom 2
France 2
United States 2
Portugal 1
Israel 1
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Trials by US State

Trials by US State for Opicapone
Location Trials
Michigan 1
California 1
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Clinical Trial Progress for Opicapone

Clinical Trial Phase

Clinical Trial Phase for Opicapone
Clinical Trial Phase Trials
Phase 4 1
Phase 3 2
Phase 1 12
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Clinical Trial Status

Clinical Trial Status for Opicapone
Clinical Trial Phase Trials
Completed 10
Not yet recruiting 3
Unknown status 1
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Clinical Trial Sponsors for Opicapone

Sponsor Name

Sponsor Name for Opicapone
Sponsor Trials
Bial - Portela C S.A. 13
Rabin Medical Center 1
Neurocrine Biosciences 1
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Sponsor Type

Sponsor Type for Opicapone
Sponsor Trials
Industry 14
Other 1
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