Last update 21 Nov 2024

Acetaminophen/Fexofenadine Hydrochloride/Phenylephrine Hydrochloride

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms
Paracetamol/fexofenadine/phenylephrine
+ [1]
Target
ADRA1 x COX x H1 receptor
Mechanism
ADRA1 agonists(Adrenergic receptor alpha-1 agonists), COX inhibitors(Cyclooxygenases inhibitors), H1 receptor antagonists(Histamine H1 receptor antagonists)
Therapeutic Areas
Infectious DiseasesRespiratory Diseases
Active Indication
Common ColdInfluenza, Human
Inactive Indication-
Originator Organization
Eurofarma Laboratórios SAEurofarma Laboratórios SA
Active Organization
Eurofarma Laboratórios SAEurofarma Laboratórios SA
Inactive Organization-
Drug Highest PhasePhase 3
First Approval Date-
Regulation-
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Structure

Molecular FormulaC9H14ClNO2
InChIKeyOCYSGIYOVXAGKQ-FVGYRXGTSA-N
CAS Registry61-76-7
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Related

1
Clinical Trials associated with Acetaminophen/Fexofenadine Hydrochloride/Phenylephrine Hydrochloride
NCT05118672 / Not yet recruitingPhase 3
A Multicenter, Randomized, Parallel-group, Double-blind, Comparative Trial of the Superiority of Paracetamol 500mg/Fexofenadine 60mg/Phenylephrine 20mg Fixed-dose Combination Versus Placebo in the Symptomatic Treatment of Flu and Cold
100 Clinical Results associated with Acetaminophen/Fexofenadine Hydrochloride/Phenylephrine Hydrochloride
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100 Translational Medicine associated with Acetaminophen/Fexofenadine Hydrochloride/Phenylephrine Hydrochloride
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100 Patents (Medical) associated with Acetaminophen/Fexofenadine Hydrochloride/Phenylephrine Hydrochloride
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100 Deals associated with Acetaminophen/Fexofenadine Hydrochloride/Phenylephrine Hydrochloride
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Common ColdPhase 3
BR
Eurofarma Laboratórios SAEurofarma Laboratórios SA
30 Nov 2024
Influenza, HumanPhase 3
BR
Eurofarma Laboratórios SAEurofarma Laboratórios SA
30 Nov 2024
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Clinical Result

Indication
Phase
Evaluation
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Approval

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Regulation

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