Last update 23 Jan 2025

Finasteride/Tamsulosin

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms
Tamsulosin/finasteride
Target
5α-reductase x α1A-AR
Mechanism
5α-reductase inhibitors(Steroid 5 alpha reductase inhibitors), α1A-AR antagonists(Alpha-1a adrenergic receptor antagonists)
Therapeutic Areas
Urogenital Diseases
Active Indication-
Inactive Indication
Prostatic Hyperplasia
Originator Organization
GL Pharm Tech Corp.GL Pharm Tech Corp.
Active Organization-
Inactive Organization
GL Pharm Tech Corp.GL Pharm Tech Corp.
Drug Highest PhasePendingPhase 1
First Approval Date-
Regulation-
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Structure/Sequence

Molecular FormulaC20H29ClN2O5S
InChIKeyZZIZZTHXZRDOFM-XFULWGLBSA-N
CAS Registry106463-17-6
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Related

1
Clinical Trials associated with Finasteride/Tamsulosin
NCT01829893
/ CompletedPhase 1IIT
Open Label, Randomized Comparative Study to Evaluate the Pharmacokinetic Characteristics Between Coadministered Finasteride Tablet and Tamsulosin HCl Tablet and GL2701 Capsule, in Healthy Subjects
100 Clinical Results associated with Finasteride/Tamsulosin
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100 Translational Medicine associated with Finasteride/Tamsulosin
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100 Patents (Medical) associated with Finasteride/Tamsulosin
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100 Deals associated with Finasteride/Tamsulosin
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Prostatic HyperplasiaPhase 1
KR
GL Pharm Tech Corp.GL Pharm Tech Corp.
01 Jan 2012
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
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Deal

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Clinical Trial

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Approval

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Regulation

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