- Trials with a EudraCT protocol (29)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
29 result(s) found for: Gastroparesis.
Displaying page 1 of 2.
EudraCT Number: 2007-003279-38 | Sponsor Protocol Number: TZP-101-CL-G004 | Start Date*: 2007-08-17 |
Sponsor Name:Tranzyme Inc. | ||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Assess the Efficacy and Safety of TZP-101 when Administered as a 30 Minute I.V. Infusion to Subjects with Severe G... | ||
Medical condition: TZP-101 will be developed as a first-in class therapy for the treatment of gastric dysmotility. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) DK (Prematurely Ended) GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2021-002254-86 | Sponsor Protocol Number: NAT-19/GPX | Start Date*: 2022-09-26 | ||||||||||||||||
Sponsor Name:Dr. Falk Pharma GmbH | ||||||||||||||||||
Full Title: Double-blind, randomised, placebo-controlled, dose-finding phase IIb trial to evaluate the efficacy, safety, and tolerability of a 12-week-treatment with Naronapride in adult participants with at l... | ||||||||||||||||||
Medical condition: idiopathic or diabetic gastroparesis | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Ongoing) PL (Ongoing) NL (Ongoing) IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000308-16 | Sponsor Protocol Number: prucalopride1 | Start Date*: 2011-10-24 | ||||||||||||||||
Sponsor Name:UZ Leuven | ||||||||||||||||||
Full Title: Prucalopride versus Placebo in Idiopathic and Diabetic Gastroparesis | ||||||||||||||||||
Medical condition: Patients with delayed gastric emptying (t1/2 for solids ≥ 109 min) either from idiopathic or diabetic origin | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-007226-19 | Sponsor Protocol Number: TZP-102-CL-G002 | Start Date*: 2009-05-15 | |||||||||||
Sponsor Name:Tranzyme Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2 Evaluation of the Safety and Efficacy of Once-Daily Administrations of TZP 102 for the Treatment of Symptomatic... | |||||||||||||
Medical condition: The medical condition to be investigated is gastroparesis due to diabetes mellitus. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) GB (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002594-33 | Sponsor Protocol Number: TZP-102-CL-G003 | Start Date*: 2011-10-14 | |||||||||||
Sponsor Name:Tranzyme, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Evaluation of the Efficacy and Safety of Once-Daily Administrations of TZP 102 for the Treatment of Symptoms Associated w... | |||||||||||||
Medical condition: The medical condition to be investigated is symptomatic gastroparesis due to diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) DK (Completed) DE (Completed) BE (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001275-21 | Sponsor Protocol Number: TAK-906-2002 | Start Date*: 2019-06-18 | |||||||||||||||||||||
Sponsor Name:Millennium Pharmaceuticals, Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited | |||||||||||||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2b Study to Evaluate the Efficacy and Safety of Twice-Daily Oral Administration of a Peripherally Acting Dopamine ... | |||||||||||||||||||||||
Medical condition: Gastroparesis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) PL (Completed) IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-002576-14 | Sponsor Protocol Number: TZP-102-CL-G004 | Start Date*: 2012-08-23 | |||||||||||
Sponsor Name:Tranzyme, Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Evaluation of the Efficacy and Safety of TZP-102 Given Orally Three Times a Day for the Treatment of Symptoms Associate... | |||||||||||||
Medical condition: The medical condition to be investigated is symptomatic gastroparesis due to diabetes mellitus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004997-23 | Sponsor Protocol Number: M0003-C201 | Start Date*: 2007-11-23 | |||||||||||
Sponsor Name:Movetis NV | |||||||||||||
Full Title: An exploratory, double-blind, randomized, stratified, placebo-controlled, repeated dose trial to investigate the efficacy of M0003 on symptoms suggestive for gastroparesis, to assess the pharmacody... | |||||||||||||
Medical condition: Symptoms suggestive for gastroparesis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) DE (Completed) LT (Completed) NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005489-46 | Sponsor Protocol Number: OPEGG | Start Date*: 2016-02-02 | |||||||||||||||||||||
Sponsor Name:Umeå University | |||||||||||||||||||||||
Full Title: Recovery of gastric function after treatment with shortacting opioids. | |||||||||||||||||||||||
Medical condition: The effect of opioids on gastric electrical activity | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023186-21 | Sponsor Protocol Number: MOT114479 | Start Date*: 2011-06-28 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Multicenter Phase II Study to Evaluate the Safety and Efficacy and Dose Response of 28 Days of Once-Daily Dosing of the Oral Motilin Receptor Agonist ... | |||||||||||||
Medical condition: Diabetic gastroparesis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) SE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003250-13 | Sponsor Protocol Number: 0099 | Start Date*: 2015-05-06 | ||||||||||||||||
Sponsor Name:Theravance Biopharma R&D, Inc. | ||||||||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group Phase 2 Study to Assess the Efficacy, Safety, and Tolerability of Velusetrag for the Treatment of Diabetic or Idiopathic ... | ||||||||||||||||||
Medical condition: diabetic or idiopathic gastroparesis. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-008175-34 | Sponsor Protocol Number: MOT111809 | Start Date*: 2009-03-31 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized Placebo-Controlled Phase II Study to Evaluate the Pharmacodynamics, Safety, Tolerability, and Pharmacokinetics of Single Doses of the Oral Motilin Receptor A... | |||||||||||||
Medical condition: Diabetic Gastroparesis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000867-18 | Sponsor Protocol Number: Codeine_I | Start Date*: 2016-03-25 |
Sponsor Name:KU Leuven | ||
Full Title: THE EFFECT OF CODEINE ON GASTRIC MOTILITY AS MEASURED WITH AN INTRAGASTRIC BALLOON | ||
Medical condition: gastroparesis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-002143-15 | Sponsor Protocol Number: RLM-MD-03 | Start Date*: 2018-11-06 | |||||||||||
Sponsor Name:Allergan Ltd. | |||||||||||||
Full Title: A 46-week, Double-blind, Placebo-controlled, Phase 3 Study with a 6-week Randomized-withdrawal Period to Evaluate the Safety and Efficacy of Relamorelin in Patients with Diabetic Gastroparesis | |||||||||||||
Medical condition: Diabetic Gastroparesis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) LV (Prematurely Ended) HU (Completed) FR (Completed) BE (Completed) DK (Prematurely Ended) BG (Completed) AT (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000406-30 | Sponsor Protocol Number: 3071-305-020 | Start Date*: 2020-07-13 | |||||||||||
Sponsor Name:Allergan Limited | |||||||||||||
Full Title: Open-label Extension Study of Relamorelin for the Treatment of Diabetic Gastroparesis | |||||||||||||
Medical condition: Diabetic Gastroparesis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010547-13 | Sponsor Protocol Number: Amisulpiride01 | Start Date*: 2010-09-16 | |||||||||||
Sponsor Name:UZLeuven | |||||||||||||
Full Title: Amisulpride versus Placebo in Functional Dyspespia with delayed gastric emptying | |||||||||||||
Medical condition: delayed gastric emptying | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005623-27 | Sponsor Protocol Number: RM-131-009 | Start Date*: 2015-04-08 | |||||||||||
Sponsor Name:Rhythm Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2b, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Efficacy of RM-131 Administered to Patients with Vomiting Symptoms and Moderate to Severe Diabetic Gastropa... | |||||||||||||
Medical condition: Vomiting symptoms in patient with moderate to severe diabetic gastroparesis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) GB (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002136-16 | Sponsor Protocol Number: RLM-MD-01 | Start Date*: 2019-04-02 | |||||||||||
Sponsor Name:Allergan Ltd. | |||||||||||||
Full Title: A 12-week, Randomized, Double-blind, Placebo-controlled, Phase 3 Study to Evaluate the Safety and Efficacy of Relamorelin in Patients with Diabetic Gastroparesis | |||||||||||||
Medical condition: Diabetic Gastroparesis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) BG (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004217-42 | Sponsor Protocol Number: 0001 | Start Date*: 2005-04-26 |
Sponsor Name:AKH Wien | ||
Full Title: Injektion von Botulinum Toxin in den Pylorus zur Behandlung von Chronic Upper Gastrointestinal Symptoms bei Diabetic Patients mit verzögerter Gastric Emptying | ||
Medical condition: Diabetes mellitus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002177-20 | Sponsor Protocol Number: RLM-MD-02 | Start Date*: 2018-11-06 | |||||||||||
Sponsor Name:Allergan Ltd. | |||||||||||||
Full Title: A 12-week, Randomized, Double-blind, Placebo-controlled, Phase 3 Study to Evaluate the Safety and Efficacy of Relamorelin in Patients with Diabetic Gastroparesis | |||||||||||||
Medical condition: Diabetic Gastroparesis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) LV (Prematurely Ended) HU (Prematurely Ended) BE (Completed) DK (Prematurely Ended) DE (Prematurely Ended) AT (Completed) RO (Prematurely Ended) | |||||||||||||
Trial results: View results |
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