Last update 21 Nov 2024

Atorvastatin/Fimasartan

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms
Atorvastatin/BR-A 657, Fimasartan/atorvastatin
Target
AT1R x HMG-CoA reductase
Mechanism
AT1R antagonists(Angiotensin II Receptor Type 1 antagonists), HMG-CoA reductase inhibitors(HMG-CoA reductase inhibitors)
Therapeutic Areas
Cardiovascular DiseasesEndocrinology and Metabolic Disease
Active Indication
DyslipidemiasHypertension
Inactive Indication
Hyperlipidemias
Originator Organization
Boryung Corp.Boryung Corp.
Active Organization
Boryung Corp.Boryung Corp.
Inactive Organization-
Drug Highest PhaseApproved
First Approval Date
KR (14 Sep 2021),
Hypertension
Regulation-
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Structure

Molecular FormulaC66H76CaF2N4O13
InChIKeyHIZONJHAVINWOX-NIJVSVLQSA-N
CAS Registry344423-98-9
View All Structures (2)

Related

2
Clinical Trials associated with Atorvastatin/Fimasartan
NCT02994745 / CompletedPhase 1
A Randomized, Open-label, Single Dose, 3x3 Partial Replicated Crossover Study to Evaluate the Pharmacokinetics and Safety/Tolerability Between a Fixed Dose Combination of Fimasartan 120mg/Atorvastatin 40mg and Co-administration of Fimasartan 120mg and Atorvastatin 40mg in Healthy Male Volunteers.
NCT02566187 / CompletedPhase 1
A Study to Compare the Pharmacokinetics of Fimasartan/Atorvastatin Combination Tablet
100 Clinical Results associated with Atorvastatin/Fimasartan
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100 Translational Medicine associated with Atorvastatin/Fimasartan
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100 Patents (Medical) associated with Atorvastatin/Fimasartan
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100 Deals associated with Atorvastatin/Fimasartan
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R&D Status

Approved
10 top approved records.
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IndicationCountry/LocationOrganizationDate
Dyslipidemias
KR
Boryung Corp.Boryung Corp.
23 Sep 2021
Hypertension
KR
Boryung Corp.Boryung Corp.
14 Sep 2021
Developing
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IndicationHighest PhaseCountry/LocationOrganizationDate
DyslipidemiasPhase 3-
Boryung Corp.Boryung Corp.
-
HypertensionPhase 3-
Boryung Corp.Boryung Corp.
-
HyperlipidemiasPreclinical
KR
Boryung Corp.Boryung Corp.
23 Dec 2016
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
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Approval

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Regulation

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