Last update 16 Sep 2025

Nifedipine/Lidocaine Hydrochloride

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms-
Target
Cav2.1 x GR x SCNA x mAChRs x β2-adrenergic receptor
Action
inhibitors, agonists, blockers,
+ [1]
Mechanism
Cav2.1 inhibitors(calcium voltage-gated channel subunit alpha1 A inhibitors), GR agonists(Glucocorticoid receptor agonists), SCNA blockers(Sodium voltage-gated channel alpha subunits blockers)
Therapeutic Areas
Digestive System Disorders
Active Indication
Fissure in Ano
Inactive Indication-
Originator Organization
CHIESI Farmaceutici SpACHIESI Farmaceutici SpA
Active Organization
Seaford Pharmaceuticals, Inc.Seaford Pharmaceuticals, Inc.
Inactive Organization-
License Organization-
Drug Highest PhaseApproved
First Approval Date-
Regulation-
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Structure/Sequence

Molecular FormulaC17H18N2O6
InChIKeyHYIMSNHJOBLJNT-UHFFFAOYSA-N
CAS Registry21829-25-4
View All Structures (2)

Related

100 Clinical Results associated with Nifedipine/Lidocaine Hydrochloride
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100 Translational Medicine associated with Nifedipine/Lidocaine Hydrochloride
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100 Patents (Medical) associated with Nifedipine/Lidocaine Hydrochloride
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100 Deals associated with Nifedipine/Lidocaine Hydrochloride
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R&D Status

10 top approved records.
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IndicationCountry/LocationOrganizationDate
Fissure in Ano
Canada
Seaford Pharmaceuticals, Inc.Seaford Pharmaceuticals, Inc.
-
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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Deal

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Core Patent

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Clinical Trial

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Approval

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Regulation

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