Last update 21 Nov 2024

ELB-245

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms
Target-
Mechanism-
Therapeutic Areas
Urogenital Diseases
Active Indication-
Inactive Indication
Urinary Bladder, OveractiveUrinary Incontinence
Originator Organization
elbion AG
Active Organization-
Inactive Organization
elbion AG
Drug Highest PhaseDiscontinuedPhase 2
First Approval Date-
Regulation-
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Related

1
Clinical Trials associated with ELB-245
NCT00439192 / TerminatedPhase 2
A Multicenter, Randomized, Double-Blind, Parallel Group, Phase II, Forced Dose Titration Study to Investigate the Efficacy and Safety of 400mg and 600mg ELB245 Given Once Daily for 12 Weeks (8 + 4 Weeks) Versus Placebo and Versus 4mg Tolterodine Given Once Daily in Patients With Incontinent Overactive Bladder (OAB)
100 Clinical Results associated with ELB-245
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100 Translational Medicine associated with ELB-245
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100 Patents (Medical) associated with ELB-245
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100 Deals associated with ELB-245
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Urinary Bladder, OveractivePhase 2
SE
elbion AG
01 Feb 2007
Urinary Bladder, OveractivePhase 2
DE
elbion AG
01 Feb 2007
Urinary Bladder, OveractivePhase 2
PL
elbion AG
01 Feb 2007
Urinary IncontinencePhase 2
SE
elbion AG
01 Feb 2007
Urinary IncontinencePhase 2
PL
elbion AG
01 Feb 2007
Urinary IncontinencePhase 2
DE
elbion AG
01 Feb 2007
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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Clinical Trial

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Approval

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Regulation

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