CompletedPhase 2NCT03282318
A Study to Investigate Efficacy, Safety, Pharmacodynamics and Pharmacokinetics of ASP6294 in the Treatment of Female Subjects With Bladder Pain Syndrome/Interstitial Cystitis
Studying Interstitial cystitis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Astellas Pharma Europe B.V.
- Principal Investigator
- Project PhysicianAstellas Pharma Europe B.V.
- Intervention
- ASP6294(drug)
- Enrollment
- 119 enrolled
- Eligibility
- 18 years · FEMALE
- Timeline
- 2017 – 2019
Study locations (28)
- Site BE32001, Leuven, Belgium
- Site CZ42002, Pilsen, Czechia
- Site DE49003, Duisburg, Germany
- Site DE49007, Duisburg, Germany
- Site DE49001, Holzminden, Germany
- Site DE49005, Markkleeberg, Germany
- Site HU36002, Budapest, Hungary
- Site HU36001, Csongrád, Hungary
- Site LV37103, Daugavpils, Latvia
- Site LV37101, Riga, Latvia
- Site LV37102, Riga, Latvia
- Site LV37105, Riga, Latvia
- Site NL31007, Sneek, Netherlands
- Site PL48009, Lodz, Poland
- Site PL48002, Szczecin, Poland
- +13 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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