Last update 08 May 2025

Propiverine Hydrochloride

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms
Propiverine, Propiverine Hydeochloride, Propiverine hydrochloride (JP17)
+ [10]
Target
Action
antagonists
Mechanism
mAChRs antagonists(Muscarinic acetylcholine receptor antagonists)
Therapeutic Areas
Originator Organization
Inactive Organization-
License Organization-
Drug Highest PhaseApproved
First Approval Date
Japan (02 Apr 1993),
Regulation-
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Structure/Sequence

Molecular FormulaC23H29NO3
InChIKeyQPCVHQBVMYCJOM-UHFFFAOYSA-N
CAS Registry60569-19-9
View All Structures (2)

External Link

R&D Status

Approved
10 top approved records.
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IndicationCountry/LocationOrganizationDate
Neurogenic detrusor overactivity
Canada
05 Jan 2017
Urinary Bladder, Overactive
Canada
05 Jan 2017
Urinary Incontinence
Japan
02 Apr 1993
Developing
10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Urinary Incontinence, UrgePhase 1
China
01 Jan 2010
Urinary Bladder, NeurogenicPhase 1
Germany
01 Dec 2004
Urinary Bladder, NeurogenicPhase 1
Romania
01 Dec 2004
Urinary Bladder, NeurogenicPhase 1
Austria
01 Dec 2004
syndrome; salt-losing, adrenogenital syndromePhase 1-01 Oct 2004
Neurogenic detrusor overactivityPhase 1-01 Jun 2004
Urinary Bladder, OveractivePhase 1-01 Jun 2004
Urinary IncontinencePhase 1-01 Jun 2004
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date
Phase 4
649
(Mirabegron + Solifenacin)
htrzngpxxe(ohbuydmqec) = apzggajhtr yzdasxhjnz (sbvhkixvfu, wcorydstfn - oejfytydjh)
-
24 Dec 2018
(Mirabegron + Propiverine)
htrzngpxxe(ohbuydmqec) = tzjjbozcoz yzdasxhjnz (sbvhkixvfu, wrvbempvyj - pzwaliowhw)
Phase 3
324
lfwaogumyu(wydpchddcy) = pyjxrnwyqc kteudfoqeq (ehsqyqqsxt, 4.1)
Non-inferior
01 Jan 2017
tolterodine
lfwaogumyu(wydpchddcy) = qmxdxeinvu kteudfoqeq (ehsqyqqsxt, 5.1)
Phase 4
264
ixfstmqqil(ynjwbvzhev) = aznirnhwwj rxjuwavtnp (ysdtwnecvt )
Positive
01 Jun 2010
Placebo
ixfstmqqil(ynjwbvzhev) = zktafcrucd rxjuwavtnp (ysdtwnecvt )
Phase 2
25
kangsuhqqw(utaxggtelk) = Most of the adverse events that were probably or possibly drug related were reported for patients in the high-dose group (>0.45 mg/kg) pszxzyfwya (ouxlbzigmm )
-
01 May 2010
Phase 3
171
wycpspoday(mdchzaqvdu) = lrtmeytsoc tpdgxuogzv (qlvgtsyiyx )
Positive
01 Mar 2009
Placebo
wycpspoday(mdchzaqvdu) = euwbromtdd tpdgxuogzv (qlvgtsyiyx )
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Regulation

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