- Trials with a EudraCT protocol (182)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
182 result(s) found for: Drug absorption.
Displaying page 1 of 10.
EudraCT Number: 2019-002587-28 | Sponsor Protocol Number: 2019-5165 | Start Date*: 2020-02-25 |
Sponsor Name:Radboudumc | ||
Full Title: ABSORB 2:An exploratie study determining the oral antibiotic drug absorption in patients with short bowel syndrome. | ||
Medical condition: short bowel syndrome, home parenteral nutrition | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-003269-46 | Sponsor Protocol Number: PedMicMida | Start Date*: 2015-04-02 |
Sponsor Name:Erasmus MC - Sophia | ||
Full Title: Pediatric microdosing midazolam: elucidating age-related changes in oral drug absorption | ||
Medical condition: Age-related changes in drug absorption and metabolism in children | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-005863-25 | Sponsor Protocol Number: FTB-11-TFV01 | Start Date*: 2012-04-26 |
Sponsor Name:Katholieke Universiteit Leuven - Pharmacotechnology and Biopharmacy | ||
Full Title: Gastrointestinal behavior of tenofovir DF in healthy volunteers | ||
Medical condition: healthy volunteers (administration of antiviral drug) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-005497-28 | Sponsor Protocol Number: PedMic | Start Date*: 2013-09-27 |
Sponsor Name:Erasmus MC - Sophia | ||
Full Title: Pediatric Microdosing: elucidating age-related changes in oral absorption | ||
Medical condition: Age-related changes in intestinal drug metabolism in children | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2016-005248-41 | Sponsor Protocol Number: DDD17Fenogal | Start Date*: 2017-05-17 |
Sponsor Name:KU Leuven - Drug Delivery and Disposition | ||
Full Title: Influence of gastrointestinal lipid digestion in the absorption of fenofibrate from a lipid-based formulation | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005129-99 | Sponsor Protocol Number: TA799-013 | Start Date*: 2021-02-10 | |||||||||||
Sponsor Name:VectivBio AG | |||||||||||||
Full Title: A multicenter, open-label, metabolic balance study to evaluate the effects of apraglutide on intestinal absorption in adult subjects with short bowel syndrome, intestinal failure (SBS-IF), and colo... | |||||||||||||
Medical condition: short bowel syndrome, intestinal failure (SBS-IF), colon-in-continuity (CIC) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002836-26 | Sponsor Protocol Number: DDD13POSA | Start Date*: 2014-01-09 |
Sponsor Name:KU Leuven - Drug Delivery & Disposition | ||
Full Title: Gastrointestinal behavior of posaconazol in healthy human volunteers | ||
Medical condition: Suspension: 105 mg posaconazol (2.6 ml Noxafil): 1)with 250 ml water 2)with 250 ml sparkling water 3)with 5 lumps of sugar, dissolved in 250 ml water 3)with 5 lumps of sugar, dissolved in 250 ml of... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-002435-18 | Sponsor Protocol Number: Diclometh-2015 | Start Date*: 2015-07-27 | |||||||||||
Sponsor Name:Aalborg University Hospital | |||||||||||||
Full Title: An Evidence Based, Translational, Cross-Over, Randomized, Double-Blind, Placebo Controlled Study to Evaluate Effectiveness of Topically applied Combination of Diclofenac and Methadone Gel (Diclome... | |||||||||||||
Medical condition: Healthy volunteers | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001715-76 | Sponsor Protocol Number: FTB13-SMV01 | Start Date*: 2013-09-05 |
Sponsor Name:KU Leuven-Drug Delivery and Disposition | ||
Full Title: Gastrointestinal behavior of simvastatin in healthy volunteers | ||
Medical condition: Healthy volunteers (administration of a hypolipidemic drug) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-002904-11 | Sponsor Protocol Number: GOC | Start Date*: 2021-09-23 |
Sponsor Name:GERMAN ONCOLOGY CENTER | ||
Full Title: Diagnostic comparison of 18F-FDG with 18F-FAPI-74 in Thyroid Cancer patients with TENIS Syndrome | ||
Medical condition: Imaging comparison of the drug under investigation on thyroid cancer patients with TENIS syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CY (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005208-14 | Sponsor Protocol Number: R17548 | Start Date*: 2012-06-18 | |||||||||||
Sponsor Name:Norfolk and Norwich University Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Innovative Gel Aid for Administering Tablets to Stroke and Other Dysphagic Patients | |||||||||||||
Medical condition: Healthy volunteers will be used in the study however the gel device being investigated has been developed with the aim of aiding swallowing in stroke and other dysphagic patients. | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-000732-34 | Sponsor Protocol Number: ABOXY_2017 | Start Date*: 2017-06-21 | ||||||||||||||||||||||||||
Sponsor Name:Mech-Sense, Dept. Gastroenterology & Hepatology, Aalborg University Hospital | ||||||||||||||||||||||||||||
Full Title: Oral Controlled Release Formulations to Patients with Gastrointestinal Dysfunction – Is the Release of Drug and the Absorption Impaired? | ||||||||||||||||||||||||||||
Medical condition: Healthy (pain) and patients (pain). | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-001601-23 | Sponsor Protocol Number: s63950 | Start Date*: 2020-06-18 |
Sponsor Name:University Hospitals of Leuven | ||
Full Title: Pharmacokinetics of apixaban in patients with short bowel syndrome requiring long term parenteral nutrition | ||
Medical condition: theoretically none (PK study), but drug is used for prevention or treatment of VTE | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Trial now transitioned) | ||
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: 2022-003275-42 | Sponsor Protocol Number: MEC-2021-0478 | Start Date*: 2023-04-13 |
Sponsor Name: | ||
Full Title: The influence of different DIets on ALECTinib pharmacokinetics in NSCLC patients; the DIALECT study. | ||
Medical condition: Weight gain is a common side effect of alectinib therapy. Semaglutide could be used as medical anti-obesity drug to prevent alectinib-induced weight gain. Since semaglutide delays gastric emptying,... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2013-005594-51 | Sponsor Protocol Number: FTB14-ABA01 | Start Date*: 2014-04-02 |
Sponsor Name:KU Leuven | ||
Full Title: Gastrointestinal behavior of abirateronacetaat in healthy volunteers | ||
Medical condition: healthy volunteers (administration of an androgen synthesis inhibitor) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-003814-37 | Sponsor Protocol Number: AKF-400 | Start Date*: 2021-11-29 | |||||||||||
Sponsor Name:Odense University Hosipital | |||||||||||||
Full Title: The effect of dicloxacillin on oral absorption of drugs | |||||||||||||
Medical condition: Healthy volunteers. (Dicloxacillin is used against infections caused by beta-lactamase-producing organisms) Testing for drug-drug interactions caused by dicloxacillin. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002826-38 | Sponsor Protocol Number: ZP1848-15073 | Start Date*: 2016-01-28 | |||||||||||
Sponsor Name:Zealand Pharma A/S | |||||||||||||
Full Title: A phase 2 trial testing ZP1848 in patients with SBS | |||||||||||||
Medical condition: Short Bowel Syndrome (SBS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004519-35 | Sponsor Protocol Number: PANC2002 | Start Date*: 2015-01-09 |
Sponsor Name:Abbott Laboratories GmbH | ||
Full Title: A Phase II, Multicenter, Parallel-Group, Active-Controlled, Randomized, Double-blind, Dose-Ranging Study to Evaluate the Efficacy and Safety of Different Doses of Creon IR in Subjects with Pancreat... | ||
Medical condition: Pancreatic exocrine Insufficiency due to Cystic Fibrosis | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) CZ (Completed) ES (Completed) GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-005928-17 | Sponsor Protocol Number: FTB-11-ITRA01 | Start Date*: 2012-04-26 |
Sponsor Name:Katholieke Universiteit Leuven - Pharmacotechnology and Biopharmacy | ||
Full Title: Gastrointestinal behavior of itraconazole in healthy volunteers | ||
Medical condition: healthy volunteers (administration of antifungal drug) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
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