Last update 31 Dec 2024

Naratriptan/Naproxen

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms-
Target
5-HT1B receptor x 5-HT1D receptor x COX-1 x COX-2
Mechanism
5-HT1B receptor agonists(Serotonin 1b (5-HT1b) receptor agonists), 5-HT1D receptor agonists(Serotonin 1d (5-HT1d) receptor agonists), COX-1 inhibitors(Cyclooxygenase-1 inhibitors)
Therapeutic Areas
Nervous System Diseases
Active Indication-
Inactive Indication
HeadacheMigraine Disorders
Originator Organization
Aché Laboratórios Farmacêuticos SAAché Laboratórios Farmacêuticos SA
Active Organization-
Inactive Organization
Aché Laboratórios Farmacêuticos SAAché Laboratórios Farmacêuticos SA
Drug Highest PhaseDiscontinuedPhase 3
First Approval Date-
Regulation-
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Structure/Sequence

Molecular FormulaC17H26ClN3O2S
InChIKeyAWEZYKMQFAUBTD-UHFFFAOYSA-N
CAS Registry143388-64-1
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Related

1
Clinical Trials associated with Naratriptan/Naproxen
NCT01390324
/ WithdrawnPhase 3
A Multicenter, National, Double-blind, Randomized Study to Evaluate the Efficacy and Safety of a Fixed-dose Combination of Naratriptan 2,5 mg + Naproxen 500 mg Relative to Efficacy and Safety of Each Monotherapy for the Acute Treatment of Migraine
100 Clinical Results associated with Naratriptan/Naproxen
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100 Translational Medicine associated with Naratriptan/Naproxen
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100 Patents (Medical) associated with Naratriptan/Naproxen
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100 Deals associated with Naratriptan/Naproxen
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
HeadachePhase 3-
Aché Laboratórios Farmacêuticos SAAché Laboratórios Farmacêuticos SA
01 Dec 2011
Migraine DisordersPhase 3-
Aché Laboratórios Farmacêuticos SAAché Laboratórios Farmacêuticos SA
01 Dec 2011
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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Approval

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Regulation

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