- Trials with a EudraCT protocol (31)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
31 result(s) found for: Pancreatic elastase.
Displaying page 1 of 2.
EudraCT Number: 2011-006019-73 | Sponsor Protocol Number: STH16190 | Start Date*: 2012-11-14 |
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | ||
Full Title: Randomized, double blind, placebo-controlled trial of Creon in patients with low faecal pancreatic elastase | ||
Medical condition: Pancreatic Insufficiency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2010-018900-10 | Sponsor Protocol Number: FLIP110 | Start Date*: 2010-05-11 | |||||||||||
Sponsor Name:Laboratoires Mayoly Spindler | |||||||||||||
Full Title: Safety and preliminary clinical activity of Yarrowia lipolytica lipase (MS1819) in patients with malabsorption syndrome due to exocrine pancreatic insufficiency resulting from chronic pancreatitis | |||||||||||||
Medical condition: Exocrine pancreatic insufficiency resulting from chronic pancreatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000562-38 | Sponsor Protocol Number: BCBe/03/Pan-CPI/002 | Start Date*: 2010-04-20 | |||||||||||
Sponsor Name:Berlin-Chemie AG | |||||||||||||
Full Title: RANDOMISED, DOUBLE BLIND, PLACEBO CONTROLLED PHASE IV TRIAL TO EVALUATE THE EFFICACY AND SAFETY OF A GASTRO-RESISTANT FILM-COATED PANCREATIN TABLET FOR LIPID DIGESTION AND ABSORPTION IN PATIENTS WI... | |||||||||||||
Medical condition: The purpose of this trial is to evaluate the clinical efficacy and safety of a gastro-resistant film-coated tablet in comparison to placebo in the treatment of pancreatic exocrine insufficiency due... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001219-11 | Sponsor Protocol Number: PNCRLPCYS3001 | Start Date*: 2015-03-31 | |||||||||||
Sponsor Name:Johnson & Johnson Pharmaceutical Research and Development, L.L.C. | |||||||||||||
Full Title: A randomized double-blind (withdrawal) phase 3 study to evaluate the efficacy and tolerability of pancrelipase MT capsules compared with placebo in the treatment of subjects with cystic fibrosis-d... | |||||||||||||
Medical condition: Cystic fibrosis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005993-12 | Sponsor Protocol Number: S245.4.012 | Start Date*: 2009-06-18 | |||||||||||
Sponsor Name:Solvay Pharmaceutical GmbH | |||||||||||||
Full Title: A three month double-blind, randomized, placebo-controlled, parallel group, multi-center study with Creon® 25.000 MMS? in subjects after an attack of acute pancreatitis suffering from pancreatic ex... | |||||||||||||
Medical condition: Pancreatic exocrine insufficiency after acute pancreatitis. Insuficiencia pancreática exocrina tras un episodio de pancreatitis aguda. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000342-12 | Sponsor Protocol Number: VIO16EPI07-01 | Start Date*: 2008-03-07 | |||||||||||
Sponsor Name:Axcan Pharma Inc. | |||||||||||||
Full Title: A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PARALLEL, PLACEBO-CONTROLLED, PHASE III STUDY TO ASSESS THE SAFETY AND EFFICACY OF VIOKASE® 16 FOR THE CORRECTION OF STEATORRHEA IN PATIENTS WITH EXOCRINE P... | |||||||||||||
Medical condition: Correction of steatorrhea (malabsorption of dietary fats) in patients with exocrine pancreatic insufficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005491-20 | Sponsor Protocol Number: 20151205 | Start Date*: 2016-08-29 |
Sponsor Name:Actavis Hungary Gyógyszermarketing és Kereskedelmi Korlátolt Felelősségű Társaság | ||
Full Title: The effect of pancreatic enzyme replacement therapy on glucose metabolism, nutritional parameters, incretin response and beta-cell function in patients with diabetes mellitus and exocrine pancreati... | ||
Medical condition: To study the patients with diabetes mellitus (type 1, 2 and 3c) and exocrine pancreatic insufficiency. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000736-24 | Sponsor Protocol Number: BCBe/03/Pan-CPI/003 | Start Date*: 2005-07-14 | |||||||||||
Sponsor Name:Berlin-Chemie AG | |||||||||||||
Full Title: RANDOMISED, DOUBLE BLIND, PLACEBO CONTROLLED PHASE IV TRIAL TO EVALUATE THE EFFICACY AND SAFETY OF AN ENTERIC-COATED PANCREATIN TABLET FOR LIPID DIGESTION AND ABSORPTION IN PATIENTS WITH PANCREATIC... | |||||||||||||
Medical condition: The purpose of this trial is to evaluate the clinical efficacy and safety of an enteric-coated pancreatin tablet in comparison to placebo in the treatment of pancreatic exocrine insufficiency due t... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-005012-80 | Sponsor Protocol Number: S245.4007 | Start Date*: 2005-03-03 |
Sponsor Name:Solvay Pharmaceuticals GmbH | ||
Full Title: Double-blind, multicenter, randomized, placebo-controlled, parallel-group study to investigate the effect of Creon 25 000 Minimicrospheres on body mass index (BMI) in patients after gastrectomy. | ||
Medical condition: Patients atleast 18 years old with total or subtotal gastrektomy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002468-89 | Sponsor Protocol Number: PANZ25STEA04-01 | Start Date*: 2004-10-28 | |||||||||||
Sponsor Name:Axcan Pharma S.A. | |||||||||||||
Full Title: A RANDOMISED, DOUBLE-BLIND, PLACEBO CONTROLLED PHASE IV TRIAL TO EVALUATE THE EFFICACY AND SAFETY OF PANCREATIN VS. PLACEBO FOR LIPID DIGESTION AND ABSORPTION IN PATIENTS WITH PANCREATIC EXOCRINE I... | |||||||||||||
Medical condition: The purpose of this clinical trial is to evaluate the clinical efficacy and safety of a capsule containing enteric-coated porcine pancreatin microfilm tablets in comparison with placebo in the trea... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020303-69 | Sponsor Protocol Number: 2010Axcan9682 | Start Date*: 2011-09-19 | |||||||||||
Sponsor Name:Erasmus MC | |||||||||||||
Full Title: Enzyme substitution in exocrine pancreatic insufficiency; Self administration against a fixed dose regimen. | |||||||||||||
Medical condition: Exocrine pancreatic insufficiency in patients with chronic pancreatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000178-21 | Sponsor Protocol Number: 0000767 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Altus Pharmaceuticals Inc. | |||||||||||||
Full Title: An Open-Label Clinical Study Evaluating the Long-Term Safety of ALTU-135 for the Treatment of Patients with Cystic Fibrosis-Related Exocrine Pancreatic Insufficiency | |||||||||||||
Medical condition: Cystic Fibrosis-Related Exocrine Pancreatic Insufficiency | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) IT (Completed) SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004854-29 | Sponsor Protocol Number: S245.4.008 | Start Date*: 2007-09-21 | |||||||||||
Sponsor Name:Abbott Products GmbH | |||||||||||||
Full Title: One week double-blind, randomized, placebo-controlled, parallel-group, multi-center study with Creon® 25000 Minimicrospheres™ in subjects with pancreatic exocrine insufficiency after pancreatic sur... | |||||||||||||
Medical condition: Pancreatic Exocrine Insufficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) BG (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001438-34 | Sponsor Protocol Number: 20-101 | Start Date*: 2005-05-23 |
Sponsor Name:McNeil Consumer and Specialty Pharmaceuticals | ||
Full Title: A Phase II, Randomized, Investigator-Blinded, Parallel-Group, Pilot Study Evaluating the Safety, Palatability and Efficacy of Four Doses of Pancrelipase Microtablets in the Treatment of Infants and... | ||
Medical condition: Cystic Fibrosis-Related Pancreatic Insufficiency and Fat Malabsorption | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-001007-38 | Sponsor Protocol Number: VITAMIN E VEDROP/06/LONGTERM/FR | Start Date*: 2007-04-25 |
Sponsor Name:ORPHAN | ||
Full Title: STUDY OF THE LONG TERM BIOLOGICAL EFFICACY AND TOLERABILITY OF VEDROP (VITAMIN E-TPGS FORMULATION) AFTER DAILY ORAL ADMINISTRATION IN 30 PAEDIATRIC PATIENTS WITH CYSTIC FIBROSIS | ||
Medical condition: Paediatric patient who present a cystic fibrosis | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-002819-10 | Sponsor Protocol Number: M13-621 | Start Date*: 2013-11-29 |
Sponsor Name:Abbott Laboratories GmbH | ||
Full Title: A Double-blind, Randomized, Multicenter, Cross-over Study to Compare the Effect of Creon N and Creon® on Fat Digestion in Subjects ≥ 12 years of Age with Pancreatic Exocrine Insufficiency Due to Cy... | ||
Medical condition: Pancreatic exocrine Insufficiency due to Cystic Fibrosis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-000171-41 | Sponsor Protocol Number: 0000726 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Altus Pharmaceuticals Inc | |||||||||||||
Full Title: A Phase III, Randomized, Double-Blind, Placebo-Controlled Clinical Study Evaluating the Efficacy and Safety of ALTU-135 Treatment in Patients with Cystic Fibrosis-Related Exocrine Pancreatic Insuff... | |||||||||||||
Medical condition: Patients with Cystic Fibrosis-Related Exocrine Pancreatic Insufficiency | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Ongoing) IT (Completed) SK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001227-45 | Sponsor Protocol Number: PHT/2017/20 | Start Date*: 2017-06-12 | |||||||||||||||||||||
Sponsor Name:Portsmouth Hospitals NHS Trust | |||||||||||||||||||||||
Full Title: Comparison of ambulatory glucose profile prior to and during pancreatic enzyme replacement therapy in patients with diabetes and pancreatic exocrine insufficiency: a single-arm phase IV trial | |||||||||||||||||||||||
Medical condition: Type 1 diabetes and type 2 diabetes mellitus Pancreatic exocrine insufficiency | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-019267-11 | Sponsor Protocol Number: MA-PA25CF10-01 | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
Sponsor Name:Axcan Pharma Inc. | |||||||||||||||||||||||
Full Title: AN OPEN-LABEL, MULTICENTER, RANDOMIZED, CROSS-OVER STUDY TO COMPARE THE SAFETY AND EFFICACY OF PANZYTRAT® 25 000 TO KREON® 25 000 IN THE CONTROL OF STEATORRHEA IN SUBJECTS AGED 7 YEARS AND OLDER WI... | |||||||||||||||||||||||
Medical condition: Correction of steathorrea associated with chronic exocrine pancreatic insufficiency in cystic fibrosis | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-000945-20 | Sponsor Protocol Number: vitk2006 | Start Date*: 2006-08-22 | |||||||||||
Sponsor Name:Barts and the London NHS Trust | |||||||||||||
Full Title: To investigate the effect of vitamin K supplementation on markers of bone turnover and bone density in adolescents and adults with cystic fibrosis | |||||||||||||
Medical condition: Cystic Fibrosis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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