226. 間質性膀胱炎(ハンナ型) Disease details / Clinical trials / Drug dev / DR info


臨床試験数 : 145 / 薬物数 : 156 - (DrugBank : 51) / 標的遺伝子数 : 64 - 標的パスウェイ数 : 146

薬物ごとの開発者(Primary Sponsor)、臨床試験情報(抜粋)です。
AGN 203818   
   Allergan
      2006   Phase 2   NCT00380783   United States;
AQX-1125   
   Aquinox Pharmaceuticals (Canada) Inc.
      2017   Phase 3   EUCTR2016-000906-12-NL   Belgium;Canada;Czech Republic;Denmark;Germany;Hungary;Latvia;Netherlands;Poland;Romania;Spain;United Kingdom;United States;
      2017   Phase 3   EUCTR2016-000906-12-ES   Belgium;Canada;Czech Republic;Denmark;Germany;Hungary;Latvia;Netherlands;Poland;Romania;Spain;United Kingdom;United States;
      2017   Phase 3   EUCTR2016-000906-12-BE   Belgium;Canada;Czech Republic;Denmark;Germany;Hungary;Latvia;Netherlands;Poland;Romania;Spain;United Kingdom;United States;
      2016   Phase 3   NCT02858453   Belgium;Canada;Czech Republic;Czechia;Denmark;Hungary;Latvia;Netherlands;Poland;Romania;Spain;United Kingdom;United States;
      2016   Phase 3   EUCTR2016-000906-12-LV   Belgium;Canada;Czech Republic;Denmark;Hungary;Latvia;Netherlands;Poland;Romania;Spain;United Kingdom;United States;
      2016   Phase 3   EUCTR2016-000906-12-HU   Belgium;Canada;Czech Republic;Denmark;Hungary;Latvia;Netherlands;Poland;Romania;Spain;United Kingdom;United States;
      2016   Phase 3   EUCTR2016-000906-12-GB   Belgium;Canada;Czech Republic;Denmark;Hungary;Latvia;Netherlands;Poland;Romania;Spain;United Kingdom;United States;
      2016   Phase 3   EUCTR2016-000906-12-DK   Belgium;Canada;Czech Republic;Denmark;Hungary;Latvia;Netherlands;Poland;Romania;Spain;United Kingdom;United States;
      2016   Phase 3   EUCTR2016-000906-12-CZ   Belgium;Canada;Czech Republic;Denmark;Hungary;Latvia;Netherlands;Poland;Romania;Spain;United Kingdom;United States;
      2013   Phase 2   NCT01882543   Canada;United States;
ASP3652   
   Astellas Pharma Europe B.V.
      2013   -   EUCTR2011-004555-39-LT   Belgium;Czech Republic;Denmark;France;Germany;Latvia;Lithuania;Netherlands;Poland;Portugal;Romania;Russian Federation;Spain;
      2012   Phase 2   NCT01613586   Belgium;Czech Republic;Czechia;Denmark;Germany;Latvia;Lithuania;Netherlands;Poland;Portugal;Romania;Russian Federation;Spain;
      2012   Phase 2   EUCTR2011-004555-39-BE   Belgium;Czech Republic;Denmark;France;Germany;Italy;Latvia;Lithuania;Netherlands;Poland;Portugal;Romania;Russian Federation;Spain;
      2012   -   EUCTR2011-004555-39-PT   Belgium;Czech Republic;Denmark;France;Germany;Latvia;Lithuania;Netherlands;Poland;Portugal;Romania;Russian Federation;Spain;
      2012   -   EUCTR2011-004555-39-PL   Belgium;Czech Republic;Denmark;France;Germany;Italy;Latvia;Lithuania;Netherlands;Poland;Portugal;Romania;Russian Federation;Spain;
      2012   -   EUCTR2011-004555-39-NL   Belgium;Czech Republic;Denmark;France;Germany;Latvia;Lithuania;Netherlands;Poland;Portugal;Romania;Russian Federation;Spain;
      2012   -   EUCTR2011-004555-39-LV   Belgium;Czech Republic;Denmark;France;Germany;Italy;Latvia;Netherlands;Poland;Portugal;Romania;Russian Federation;Spain;
      2012   -   EUCTR2011-004555-39-ES   Belgium;Czech Republic;Denmark;France;Germany;Latvia;Netherlands;Poland;Portugal;Romania;Russian Federation;Spain;
      2012   -   EUCTR2011-004555-39-DK   Belgium;Czech Republic;Denmark;France;Germany;Latvia;Lithuania;Netherlands;Poland;Portugal;Romania;Russian Federation;Spain;
      2012   -   EUCTR2011-004555-39-DE   Belgium;Czech Republic;Denmark;France;Germany;Latvia;Lithuania;Netherlands;Poland;Portugal;Romania;Russian Federation;Spain;
      2012   -   EUCTR2011-004555-39-CZ   Belgium;Czech Republic;Denmark;France;Germany;Latvia;Lithuania;Netherlands;Poland;Portugal;Romania;Russian Federation;Spain;
ASP6294   
   Astellas Pharma Europe B.V.
      2017   Phase 2   NCT03282318   Belgium;Czechia;Germany;Hungary;Latvia;Netherlands;Poland;Russian Federation;Spain;United Kingdom;
      2017   Phase 2   EUCTR2016-004138-12-PL   Belgium;Czech Republic;Germany;Hungary;Latvia;Netherlands;Poland;Russian Federation;Spain;United Kingdom;
      2017   Phase 2   EUCTR2016-004138-12-NL   Belgium;Czech Republic;Germany;Hungary;Latvia;Netherlands;Poland;Russian Federation;Spain;United Kingdom;
      2017   Phase 2   EUCTR2016-004138-12-LV   Belgium;Czech Republic;Germany;Hungary;Latvia;Netherlands;Poland;Russian Federation;Spain;United Kingdom;
      2017   Phase 2   EUCTR2016-004138-12-HU   Belgium;Czech Republic;Germany;Hungary;Latvia;Netherlands;Poland;Russian Federation;Spain;United Kingdom;
      2017   Phase 2   EUCTR2016-004138-12-GB   Belgium;Czech Republic;Germany;Hungary;Latvia;Netherlands;Poland;Russian Federation;Spain;United Kingdom;
      2017   Phase 2   EUCTR2016-004138-12-ES   Belgium;Czech Republic;Germany;Hungary;Latvia;Netherlands;Poland;Russian Federation;Spain;United Kingdom;
      2017   Phase 2   EUCTR2016-004138-12-DE   Belgium;Czech Republic;Germany;Hungary;Latvia;Netherlands;Poland;Russian Federation;Spain;United Kingdom;
      2017   Phase 2   EUCTR2016-004138-12-CZ   Belgium;Czech Republic;Germany;Hungary;Latvia;Netherlands;Poland;Russian Federation;Spain;United Kingdom;
      2017   Phase 2   EUCTR2016-004138-12-BE   Belgium;Czech Republic;Germany;Hungary;Latvia;Netherlands;Poland;Russian Federation;Spain;United Kingdom;
Adalimumab   
   ICStudy, LLC
      2011   Phase 3   NCT01295814   United States;
Alkalinized Lidocaine-Heparin   
   Urigen
      2006   Phase 2   NCT00256542   United States;
AlloRx   
   The Foundation for Orthopaedics and Regenerative Medicine
      2021   Phase 1   NCT05147779   Antigua and Barbuda;
Amitriptyline   
   National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
      2005   Phase 3   NCT00124306   Canada;United States;
BOTOX 100U in normal saline   
   Buddhist Tzu Chi General Hospital
      2021   Phase 2   NCT05275647   Taiwan;
BOTOX 200U in normal saline   
   Buddhist Tzu Chi General Hospital
      2014   Phase 2   NCT02247557   Taiwan;
Bladder Instillations   
   William Beaumont Hospitals
      2017   Phase 2   NCT02870738   United States;
Bladder instillation WITH triamcinolone acetonide   
   Olivia Cardenas-Trowers, M.D.
      2019   Phase 3   NCT03463915   United States;
Bladder instillation WITHOUT triamcinolone acetonide   
   Olivia Cardenas-Trowers, M.D.
      2019   Phase 3   NCT03463915   United States;
Bladder instillation with heparin/ lidocaine   
   Scripps Health
      2012   Phase 2   NCT01048177   United States;
Botox   
   University of Washington
      2004   Phase 4   NCT00194610   United States;
   research office urology VUmc
      2008   -   EUCTR2007-005164-27-NL   Netherlands;
Botulinum toxin A   
   Buddhist Tzu Chi General Hospital
      2012   Phase 2   NCT01969773   Taiwan;
Buckwheat   
   Center for Pharma-Food Research, Graduate School of Pharmaceutical Sciences, University of Shizuoka
      2017   -   JPRN-UMIN000029113   Japan;
Bupivacaine   
   Case Western Reserve University
      2009   -   NCT01616992   United States;
Bupivacaine, triamcinolone, and heparin (BTH)   
   NorthShore University HealthSystem
      2011   Phase 4   NCT05223244   -
Cannabidiol vaginal suppository   
   University of New Mexico
      2021   Phase 1   NCT04349930   United States;
Capsaicin   
   National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
      1995   Phase 1/Phase 2   NCT00004316   -
Certolizumab pegol   
   ICStudy, LLC
      2015   Phase 3   NCT02497976   United States;
Ciklosporin   
   Ingrid Ehrén
      2005   -   EUCTR2005-000890-23-SE   Sweden;
Combination Product: Hyperbaric Oxygen Therapy-   
   University of California, San Diego
      2017   Early Phase 1   NCT03143920   United States;
Cyclosporine   
   The Cleveland Clinic
      2013   Phase 2   NCT01990898   United States;
DMSO   
   Assaf-Harofeh Medical Center
      2010   -   NCT01069263   Israel;
   Deparment of Urology, Medical Science, University of Fukui
      2005   -   JPRN-UMIN000003172   Japan;
   Department of Urology, Hamamatsu University School of Medicine
      2004   -   JPRN-UMIN000027494   Japan;
   Urology, Hokkaido University Graduate School of Medicine
      2014   -   JPRN-UMIN000014860   Japan;
DMSO cocktail   
   Assaf-Harofeh Medical Center
      2009   -   NCT01074567   Israel;
Desert Harvest Aloe Vera Capsules   
   Wake Forest University Health Sciences
      2022   Early Phase 1   NCT04734106   United States;
Dexmedetomidine   
   University of Rochester
      2010   Phase 4   NCT01195116   United States;
Dextrose   
   National Defense Medical Center, Taiwan
      2019   -   NCT04821882   Taiwan;
Dimethyl sulfoxide   
   Capital District Health Authority, Canada
      2006   Phase 2   NCT00317070   Canada;
   IBSA
      2011   -   EUCTR2010-021556-25-IT   Italy;
   Kyorin Pharmaceutical Co.,LTD
      2017   Phase 3   JPRN-JapicCTI-173566   Japan;
Dimethyl sulfoxide (DMSO)   
   NorthShore University HealthSystem
      2011   Phase 4   NCT05223244   -
ERB-041   
   Wyeth is now a wholly owned subsidiary of Pfizer
      2006   -   NCT00275379   Austria;Germany;United States;
Flavoxate   
   Torimoto Kazumasa
      2021   Phase 2   JPRN-jRCTs051210106   Japan;
Fospropofol (Lusedra®) 10   
   Grace Shih, MD
      2011   -   NCT01378754   United States;
Fospropofol (Lusedra®) 12   
   Grace Shih, MD
      2011   -   NCT01378754   United States;
Fospropofol (Lusedra®) 6.5   
   Grace Shih, MD
      2011   -   NCT01378754   United States;
Fremanezumab   
   Teva Branded Pharmaceutical Products R&D, Inc.
      2020   Phase 2   NCT04447729   -
Gefapixant   
   Afferent Pharmaceuticals, Inc.
      2012   Phase 2   NCT01569438   United States;
Glycine   
   Kimio Sugaya (Kitakami Central Hospital, and Southern Knights' Laboratory LLP)
      2013   -   JPRN-JMA-IIA00113   Japan;
Gralise   
   Shirley Ryan AbilityLab
      2012   Phase 4   NCT01678911   United States;
Heparin   
   Department of Urology and Renal transplantation, Nagasaki University Hospital
      2016   -   JPRN-UMIN000027918   Japan;
   Department of Urology, Mitsui Memorial Hospital
      2016   Phase 2,3   JPRN-UMIN000026714   Japan;
   University of Tokushima
      2011   Phase 2   JPRN-UMIN000006387   Japan;
   Urigen
      2015   Phase 2   NCT02591199   United States;
Heparin & Alkalinized Lidocaine Bladder Instillation   
   Walter Reed National Military Medical Center
      2020   Phase 2   NCT04401176   United States;
High Density Surface Electromyographic, precision botulinum neurotoxin injection guidance medical device   
   HillMed Inc.
      2023   Early Phase 1   NCT05062902   United States;
Hyaluronic Acid and Chondroitin Sulfate   
   Samsung Medical Center
      2017   -   NCT03463499   Korea, Republic of;
Hyaluronic acid/chondroitin sulfate   
   Asan Medical Center
      2013   -   NCT01813565   Korea, Republic of;
Hydrogen   
   Koushinkai Hospital
      2008   Phase 2,3   JPRN-UMIN000001253   Japan;
IC Cocktail   
   Capital District Health Authority, Canada
      2006   Phase 2   NCT00317070   Canada;
IPD® (Japanese tradename)   
   Astellas Pharma Europe B.V.
      2006   Phase 2   EUCTR2005-003367-23-DK   Denmark;Germany;Sweden;
      2006   -   EUCTR2005-003367-23-SE   Germany;Sweden;
      2006   -   EUCTR2005-003367-23-DE   Germany;Sweden;
IPD® (suplatast tosilate)   
   Astellas Pharma Europe B.V.
      2006   Phase 2   EUCTR2005-003367-23-DK   Denmark;Germany;Sweden;
      2006   -   EUCTR2005-003367-23-SE   Germany;Sweden;
Injections on posterior bladder wall excluding the trigone   
   Wake Forest University Health Sciences
      2014   Phase 4   NCT02297100   United States;
Injections upper aspect of trigone of urinary bladder   
   Wake Forest University Health Sciences
      2014   Phase 4   NCT02297100   United States;
Interferential current   
   Cairo University
      2019   -   NCT03844581   Egypt;
Intermittent Exposure to Oxygen via Oro-Nasal Mask   
   University of South Florida
      2016   -   NCT03693001   -
Intravesical onabotulinumtoxinA injection   
   Buddhist Tzu Chi General Hospital
      2015   Phase 2   NCT03076762   Taiwan;
JNJ-42160443   
   Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
      2010   Phase 2   NCT01060254   Canada;United States;
KRP-116D   
   Kyorin Pharmaceutical Co.,LTD
      2017   Phase 3   JPRN-JapicCTI-173566   Japan;
Ketorolac Tromethamine   
   Citrus Valley Medical Research, Inc.
      2012   Phase 4   NCT02000401   United States;
LP-08   
   Lipella Pharmaceuticals, Inc.
      2015   Phase 2   NCT01393223   United States;
LiRIS   
   Allergan
      2013   Phase 2   NCT01824303   Canada;United States;
LiRIS low dose and LiRIS high dose   
   Allergan
      2010   Phase 1   NCT01150565   Canada;
LiRIS®   
   Allergan
      2015   Phase 2   NCT02395042   Canada;United States;
      2013   Phase 1   NCT01879683   United States;
Lidocaine   
   Department of Urology and Renal transplantation, Nagasaki University Hospital
      2016   -   JPRN-UMIN000027918   Japan;
   Department of Urology, Mitsui Memorial Hospital
      2016   Phase 2,3   JPRN-UMIN000026714   Japan;
   Johns Hopkins University
      2015   -   NCT02517996   United States;
   North Shore Long Island Jewish Health System
      2009   -   NCT00823030   United States;
   Urigen
      2015   Phase 2   NCT02591199   United States;
Lidocaine Releasing Intravesical System - LiRIS®   
   Allergan
      2011   Phase 2   NCT01475253   Canada;United States;
Liposome encapsulated BoNT-A   
   Buddhist Tzu Chi General Hospital
      2014   Phase 2   NCT02247557   Taiwan;
Liposomes   
   Kenneth Peters, MD
      2012   -   NCT01731470   United States;
      2010   -   NCT01083979   United States;
Low-dose naltrexone   
   NorthShore University HealthSystem
      2021   Phase 4   NCT04313972   United States;
MN-001 BID   
   MediciNova
      2005   Phase 2   NCT00295854   United States;
MR-MC-01   
   Asan Medical Center
      2020   Phase 1   NCT04610359   Korea, Republic of;
Metoprolol Tartrate Oral Tablet   
   Medical College of Wisconsin
      2017   Phase 4   NCT03008382   United States;
Mirabegron   
   Department of Urology, Graduate school of medicine, University of Tokyo
      2012   -   JPRN-UMIN000008484   Japan;
   Philadelphia Urosurgical Associates
      2016   Phase 3   NCT02787083   United States;
Mycofenolate Mofetil (MMF)   
   National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
      2007   Phase 3   NCT00451867   Canada;United States;
NALOXONE HYDROCHLORIDE   
   Mundipharma Research GmbH & Co. KG
      2010   Phase 2   EUCTR2009-018118-21-GB   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-HU   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-CZ   Czech Republic;Germany;Hungary;United Kingdom;
      -   -   EUCTR2009-018118-21-DE   Czech Republic;Germany;Hungary;United Kingdom;
Naltrexone   
   Stanford University
      2020   Phase 2   NCT04450316   United States;
Normal Saline   
   University of Rochester
      2010   Phase 4   NCT01195116   United States;
Normal saline   
   Lipella Pharmaceuticals, Inc.
      2015   Phase 2   NCT01393223   United States;
Normal saline instillation   
   Buddhist Tzu Chi General Hospital
      2012   Phase 2   NCT01969773   Taiwan;
Nortriptyline   
   Duke University
      2019   Phase 2   NCT03844412   United States;
OXN 10/5 mg PR   
   Mundipharma Research GmbH & Co. KG
      2010   Phase 2   EUCTR2009-018118-21-GB   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-HU   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-CZ   Czech Republic;Germany;Hungary;United Kingdom;
      -   -   EUCTR2009-018118-21-DE   Czech Republic;Germany;Hungary;United Kingdom;
OXN 20/10 mg PR   
   Mundipharma Research GmbH & Co. KG
      2010   Phase 2   EUCTR2009-018118-21-GB   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-HU   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-CZ   Czech Republic;Germany;Hungary;United Kingdom;
      -   -   EUCTR2009-018118-21-DE   Czech Republic;Germany;Hungary;United Kingdom;
OXN 5/2.5 mg PR   
   Mundipharma Research GmbH & Co. KG
      2010   Phase 2   EUCTR2009-018118-21-GB   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-HU   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-CZ   Czech Republic;Germany;Hungary;United Kingdom;
      -   -   EUCTR2009-018118-21-DE   Czech Republic;Germany;Hungary;United Kingdom;
OXYCODONE HYDROCHLORIDE   
   Mundipharma Research GmbH & Co. KG
      2010   Phase 2   EUCTR2009-018118-21-GB   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-HU   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-CZ   Czech Republic;Germany;Hungary;United Kingdom;
      -   -   EUCTR2009-018118-21-DE   Czech Republic;Germany;Hungary;United Kingdom;
Omalizumab   
   IRCCS Policlinico S. Matteo
      2009   Phase 3   NCT01294878   Italy;
Onabotulinum Toxin A   
   Walter Reed National Military Medical Center
      2020   Phase 2   NCT04401176   United States;
Onabotulinumtoxin A   
   Wake Forest University Health Sciences
      2014   Phase 4   NCT02297100   United States;
Oxycodone naloxone prolonged release tablets   
   Mundipharma Research GmbH & Co KG
      2010   Phase 2   NCT01197261   Czech Republic;Czechia;Germany;Hungary;Poland;United Kingdom;
Oxycodone/naloxone prolonged release t   
   Mundipharma Research GmbH & Co. KG
      2010   -   EUCTR2009-018118-21-HU   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-CZ   Czech Republic;Germany;Hungary;United Kingdom;
      -   -   EUCTR2009-018118-21-DE   Czech Republic;Germany;Hungary;United Kingdom;
Oxycodone/naloxone prolonged release tablets 10/   
   Mundipharma Research GmbH & Co. KG
      2010   Phase 2   EUCTR2009-018118-21-GB   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-HU   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-CZ   Czech Republic;Germany;Hungary;United Kingdom;
      -   -   EUCTR2009-018118-21-DE   Czech Republic;Germany;Hungary;United Kingdom;
Oxycodone/naloxone prolonged release tablets 20/   
   Mundipharma Research GmbH & Co. KG
      2010   Phase 2   EUCTR2009-018118-21-GB   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-HU   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-CZ   Czech Republic;Germany;Hungary;United Kingdom;
      -   -   EUCTR2009-018118-21-DE   Czech Republic;Germany;Hungary;United Kingdom;
Oxycodone/naloxone prolonged release tablets 5/   
   Mundipharma Research GmbH & Co. KG
      2010   Phase 2   EUCTR2009-018118-21-GB   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-HU   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-CZ   Czech Republic;Germany;Hungary;United Kingdom;
      -   -   EUCTR2009-018118-21-DE   Czech Republic;Germany;Hungary;United Kingdom;
Oxygen   
   Assaf-Harofeh Medical Center
      2010   -   NCT01069263   Israel;
Oxytocin   
   University of Alabama at Birmingham
      2010   Phase 4   NCT00919802   United States;
Ozone   
   Anhembi Morumbi University
      2020   Phase 2   NCT04789135   Brazil;
PD 0299685   
   Pfizer Ltd., Ramsgate Road, Sandwich, Kent, CT13 9NJ, UK
      2008   -   EUCTR2008-002421-37-FI   Denmark;Finland;France;Germany;
      2008   -   EUCTR2008-002421-37-DK   Denmark;Finland;France;Germany;
      -   -   EUCTR2008-002421-37-DE   Denmark;Finland;France;Germany;
PD 0299685 at 15mg BID   
   Pfizer
      2008   Phase 2   NCT00739739   Canada;Denmark;Finland;France;Germany;United States;
PD 0299685 at 30mg BID   
   Pfizer
      2008   Phase 2   NCT00739739   Canada;Denmark;Finland;France;Germany;United States;
PD-0299685   
   Pfizer Ltd
   Ramsgate Road,Sandwich,Kent CT13 9NJ
PF-04383119   
   Pfizer
      2008   Phase 2   NCT00601484   United States;
   Pfizer Inc., 235 East 42nd Street, New York, NY 10017
      2010   Phase 2   EUCTR2009-014597-17-SK   Belgium;Finland;Germany;Slovakia;Spain;Sweden;
      2010   -   EUCTR2009-014597-17-SE   Belgium;Finland;Germany;Spain;Sweden;
      2010   -   EUCTR2009-014597-17-FI   Belgium;Finland;Germany;Spain;Sweden;
      2010   -   EUCTR2009-014597-17-DE   Belgium;Finland;Germany;Spain;Sweden;
      2009   -   EUCTR2009-014597-17-BE   Belgium;Finland;Germany;Spain;Sweden;
   Pfizer, S.A.
      2010   -   EUCTR2009-014597-17-ES   Belgium;Finland;Germany;Spain;Sweden;
Pelvic Floor Physical Therapy   
   William Beaumont Hospitals
      2017   Phase 2   NCT02870738   United States;
Pentosan polysulfate sodium   
   Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
      2003   Phase 4   NCT00086684   Canada;United States;
Peppermint oil   
   University of Louisville
      2021   Phase 1/Phase 2   NCT04845217   United States;
Placebo   
   Kyorin Pharmaceutical Co.,LTD
      2017   Phase 3   JPRN-JapicCTI-173566   Japan;
Platelet enriched plasma   
   Mansoura University
      2019   Phase 1/Phase 2   NCT04118946   Egypt;
Platelet-Rich Plasma   
   Buddhist Tzu Chi General Hospital
      2017   Phase 1   NCT03104361   Taiwan;
Prograf   
   Jukka Sairanen
      2008   -   EUCTR2008-001501-42-FI   Finland;
Propiverine Hydrochloride   
   Cairo University
      2019   -   NCT03844581   Egypt;
RN624, RI624   
   Pfizer Inc., 235 East 42nd Street, New York, NY 10017
      2010   Phase 2   EUCTR2009-014597-17-SK   Belgium;Finland;Germany;Slovakia;Spain;Sweden;
      2010   -   EUCTR2009-014597-17-SE   Belgium;Finland;Germany;Spain;Sweden;
      2010   -   EUCTR2009-014597-17-FI   Belgium;Finland;Germany;Spain;Sweden;
      2010   -   EUCTR2009-014597-17-DE   Belgium;Finland;Germany;Spain;Sweden;
      2009   -   EUCTR2009-014597-17-BE   Belgium;Finland;Germany;Spain;Sweden;
   Pfizer, S.A.
      2010   -   EUCTR2009-014597-17-ES   Belgium;Finland;Germany;Spain;Sweden;
SANDIMMUN   
   Oulu University Hospital
      2015   -   EUCTR2015-004495-30-FI   Finland;
SI-722   
   Seikagaku Corporation
      2020   Phase 1/Phase 2   NCT04208087   United States;
Sandimmun Neoral   
   Ingrid Ehrén
      2005   -   EUCTR2005-000890-23-SE   Sweden;
Sham Cystoscopy Procedure   
   Allergan
      2011   Phase 2   NCT01475253   Canada;United States;
Sildenafil   
   The First Af?liated Hospital of Wenzhou Medical College
      2009   -   ChiCTR-TRC-13003938   China;
Suplatast tosilate   
   Astellas Pharma Europe B.V.
      2006   -   EUCTR2005-003367-23-DE   Germany;Sweden;
TTI-1612   
   Trillium Therapeutics Inc.
      2012   Phase 1   NCT01559961   Canada;
Tanezumab   
   Pfizer
      2010   Phase 2   NCT00999518   Belgium;Canada;Finland;Germany;Hong Kong;India;Japan;Korea, Republic of;Poland;Romania;Russian Federation;Slovakia;South Africa;Spain;Sweden;Taiwan;United States;
      2009   Phase 1   NCT01030640   United States;
   Pfizer Inc., 235 East 42nd Street, New York, NY 10017
      2010   Phase 2   EUCTR2009-014597-17-SK   Belgium;Finland;Germany;Slovakia;Spain;Sweden;
      2010   -   EUCTR2009-014597-17-SE   Belgium;Finland;Germany;Spain;Sweden;
      2010   -   EUCTR2009-014597-17-FI   Belgium;Finland;Germany;Spain;Sweden;
      2010   -   EUCTR2009-014597-17-DE   Belgium;Finland;Germany;Spain;Sweden;
      2009   -   EUCTR2009-014597-17-BE   Belgium;Finland;Germany;Spain;Sweden;
   Pfizer, S.A.
      2010   -   EUCTR2009-014597-17-ES   Belgium;Finland;Germany;Spain;Sweden;
Targinact 10 mg/5 mg prolonged-release tablets   
   Mundipharma Research GmbH & Co. KG
      2010   Phase 2   EUCTR2009-018118-21-GB   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-HU   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-CZ   Czech Republic;Germany;Hungary;United Kingdom;
      -   -   EUCTR2009-018118-21-DE   Czech Republic;Germany;Hungary;United Kingdom;
Targinact 20mg/10 mg prolonged-release tablets   
   Mundipharma Research GmbH & Co. KG
      2010   Phase 2   EUCTR2009-018118-21-GB   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-HU   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-CZ   Czech Republic;Germany;Hungary;United Kingdom;
      -   -   EUCTR2009-018118-21-DE   Czech Republic;Germany;Hungary;United Kingdom;
Targinact 5mg/2.5 mg prolonged-release tablets   
   Mundipharma Research GmbH & Co. KG
      2010   Phase 2   EUCTR2009-018118-21-GB   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-HU   Czech Republic;Germany;Hungary;United Kingdom;
      2010   -   EUCTR2009-018118-21-CZ   Czech Republic;Germany;Hungary;United Kingdom;
      -   -   EUCTR2009-018118-21-DE   Czech Republic;Germany;Hungary;United Kingdom;
Tissue examination for protein- and mRNA-expression of NO   
   Copenhagen University Hospital at Herlev
      2006   -   NCT00253006   Denmark;
Tramadol   
   Departmen of Urology, The University of Tokyo Hospital
      2014   -   JPRN-UMIN000009197   Japan;
URG101   
   Urigen
      2015   Phase 2   NCT02591199   United States;
      2007   Phase 2   NCT00517868   United States;
Urodynamic study   
   North Shore Long Island Jewish Health System
      2009   -   NCT00823030   United States;
Water   
   Koushinkai Hospital
      2008   Phase 2,3   JPRN-UMIN000001253   Japan;
YM672 (IPD®)   
   Astellas Pharma Europe B.V.
      2006   Phase 2   EUCTR2005-003367-23-DK   Denmark;Germany;Sweden;
      2006   -   EUCTR2005-003367-23-SE   Germany;Sweden;
      2006   -   EUCTR2005-003367-23-DE   Germany;Sweden;
lidocaine/5 mg/ml estradiol compound cream   
   Duke University
      2019   Phase 2   NCT03844412   United States;
sodium chondroitin sulfate   
   Watson Pharmaceuticals
      2009   Phase 2   NCT00919113   United States;