- Trials with a EudraCT protocol (43)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
43 result(s) found for: Grapefruit Juice.
Displaying page 1 of 3.
EudraCT Number: 2017-001284-20 | Sponsor Protocol Number: BIOGIO | Start Date*: 2017-07-05 |
Sponsor Name:Erasmus MC Cancer Institute | ||
Full Title: The effects of the proton pump inhibitor esomeprazole on the bioavailability of afatinib (Giotrif®) in patients with non-small cell lung cancer (NSCLC) 'the BIO-GIO study' | ||
Medical condition: Non small cell lung cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005784-17 | Sponsor Protocol Number: REGORA | Start Date*: 2016-05-19 |
Sponsor Name:Erasmus MC cancer institute | ||
Full Title: The effects of the proton pump inhibitor esomeprazole on the bioavailability of regorafenib in patients with a metastatic colorectal cancer (mCRC) or gastrointestinal stromal tumour (GIST). | ||
Medical condition: GIST and mCRC patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003849-32 | Sponsor Protocol Number: AGI003-007 (ARDIS-3) | Start Date*: 2007-10-22 | |||||||||||
Sponsor Name:AGI Therapeutics Research Ltd | |||||||||||||
Full Title: An Open-label, Roll-over Safety Study of AGI-003 (Arverapamil) in the Treatment of Irritable Bowel Syndrome with Diarrhea (IBS-D) | |||||||||||||
Medical condition: Irritable Bowel Syndrome with Diarrhea (IBS-D) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) PL (Prematurely Ended) CZ (Prematurely Ended) LT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-003265-38 | Sponsor Protocol Number: PTC743-NEU-005-FA | Start Date*: 2022-10-22 |
Sponsor Name:PTC Therapeutics, Inc. | ||
Full Title: An Open-Label Study to Evaluate Pharmacokinetics, Safety, and Efficacy of Vatiquinone in Children With Friedreich Ataxia Younger Than 7 Years of Age | ||
Medical condition: Friedreich Ataxia | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: (No results available) |
EudraCT Number: 2017-004465-27 | Sponsor Protocol Number: COCA | Start Date*: 2018-02-01 |
Sponsor Name:Erasmus MC Cancer Institute | ||
Full Title: The effects of the proton pump inhibitor esomeprazole alone or in combination with Coca-Cola on the absorption of Capecitabine in patients with colorectal cancer or other solid tumours ' the COCA s... | ||
Medical condition: Colorectal carcinoma or other solid tumours | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003553-82 | Sponsor Protocol Number: AGI003-003 (ARDIS-1) | Start Date*: 2007-10-22 | |||||||||||
Sponsor Name:AGI Therapeutics Research Ltd | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Study of AGI-003 (Arverapamil) in the Treatment of Irritable Bowel Syndrome with Diarrhea (IBS-D) | |||||||||||||
Medical condition: Irritable Bowel Syndrome with Diarrhea (IBS-D) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) LT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000276-41 | Sponsor Protocol Number: SUMO | Start Date*: 2020-03-05 |
Sponsor Name:Erasmus MC | ||
Full Title: Study on the effects of an OCT2/MATE1 substrate (metformin) and inhibitor (cimetidine) on the exposure of trifluridine/tipiracil (Lonsurf®) in patients with metastatic colorectal cancer (mCRC). | ||
Medical condition: patients with mCRC with an indication for lonsurf treatment. | ||
Disease: | ||
Population Age: | Gender: | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-004008-71 | Sponsor Protocol Number: ELDORADO | Start Date*: 2017-01-19 |
Sponsor Name:Erasmus MC Cancer Institute | ||
Full Title: The effect of curcumin and piperine on the pharmacokinetics of tamoxifen in patients with estrogen receptor positive breast cancer ‘the ELDORADO study’ | ||
Medical condition: Estrogen receptor positive breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-005213-22 | Sponsor Protocol Number: SUPREMES-01 | Start Date*: Information not available in EudraCT |
Sponsor Name:Charite Universitätsmedizin Berlin | ||
Full Title: SUPREMES - Sunphenon in progressive forms of multiple sclerosis | ||
Medical condition: primary and secondary progressive forms of multiple sclerosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-009656-20 | Sponsor Protocol Number: SUN-AK | Start Date*: 2009-05-07 |
Sponsor Name:Charite Universitaetsmedizin Berlin | ||
Full Title: Sunphenon EGCg (Epigallocatechin-Gallat) in the early stage of Alzheimer´s Disease | ||
Medical condition: Alzheimer´s disease (early stage) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2019-002954-21 | Sponsor Protocol Number: QBGJ398-201 | Start Date*: 2020-03-31 | |||||||||||
Sponsor Name:QED Therapeutics, Inc. | |||||||||||||
Full Title: Phase 2, Open-Label, Dose-Escalation and Dose-Expansion Study of Infigratinib, an FGFR 1-3-Selective Tyrosine Kinase Inhibitor, in Children with Achondroplasia: PROPEL 2 | |||||||||||||
Medical condition: Achondroplasia in Children | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002550-39 | Sponsor Protocol Number: PDY13949 | Start Date*: 2016-10-20 | ||||||||||||||||
Sponsor Name:Genzyme Corporation | ||||||||||||||||||
Full Title: 4-part, open-label, multicenter, multinational study of the safety, tolerability, pharmacokinetics, pharmacodynamic, and exploratory efficacy of venglustat in combination with Cerezyme in adult pat... | ||||||||||||||||||
Medical condition: Gaucher disease | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001038-34 | Sponsor Protocol Number: NK-104-305 | Start Date*: 2006-02-03 | |||||||||||
Sponsor Name:Kowa Research Europe Ltd. | |||||||||||||
Full Title: STUDY OF PITAVASTATIN 4 MG vs. ATORVASTATIN 20 MG (FOLLOWING UP-TITRATION) IN PATIENTS WITH TYPE II DIABETES MELLITUS AND COMBINED DYSLIPIDEMIA | |||||||||||||
Medical condition: Type II Diabetes Mellitus and Combined Dyslipidemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003169-19 | Sponsor Protocol Number: CYC-201 | Start Date*: 2009-11-09 | |||||||||||
Sponsor Name:Sigmoid Pharma Ltd | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Study of a Controlled Release Minicapusle Formulation of Ciclosporin (CyCol™) in the Treatment of Ulcerative Colitis | |||||||||||||
Medical condition: Ulcerative colitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014908-57 | Sponsor Protocol Number: POA1004 | Start Date*: 2009-09-03 | |||||||||||
Sponsor Name:Purdue Pharma L.P. | |||||||||||||
Full Title: CAPSAICIN CHALLENGE STUDY TO INVESTIGATE THE POTENTIAL ANALGESIC EFFECTS OF V113741 IN HEALTHY MALE SUBJECTS | |||||||||||||
Medical condition: Modeling inflammatory and neuropathic pain | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-010660-42 | Sponsor Protocol Number: ORA2 | Start Date*: 2009-08-13 |
Sponsor Name:BOWS Pharmaceuticals AG | ||
Full Title: A double-blind two part placebo-controlled study consisting of a single ascending and multiple-dose tolerance study of peroral insulin in patients with Type 2 diabetes | ||
Medical condition: Type 2 diabetes | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-020953-14 | Sponsor Protocol Number: PosaBupreversion1.0 | Start Date*: 2010-08-12 |
Sponsor Name:Derartment of Anaesthesiology and Intensive Care, Turku University Hospital | ||
Full Title: Effects of posaconazole and voriconazole on the pharmacokinetics and pharmacodynamics of sublingual buprenorphine: A three-phase double-blind cross-over study in healthy subjects. | ||
Medical condition: - healty volunteer subjects - The study is aimed to examine the possible interactions of low-dose sublingual buprenorphine with posaconazole and voriconazole. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002461-66 | Sponsor Protocol Number: CABL001A2301 | Start Date*: 2017-10-09 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A phase 3, multi-center, open-label, randomized study of oral ABL001 versus bosutinib in patients with Chronic Myelogenous Leukemia in chronic phase (CML-CP), previously treated with 2 or more tyro... | |||||||||||||
Medical condition: Chronic Myelogenous Leukemia in chronic phase (CML-CP), previously treated with 2 or more tyrosine kinase inhibitors | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Ongoing) CZ (Ongoing) ES (Ongoing) BG (Completed) DE (Ongoing) GB (GB - no longer in EU/EEA) FR (Ongoing) NL (Ongoing) BE (Ongoing) IT (Ongoing) RO (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004043-23 | Sponsor Protocol Number: IDX-04B-001 | Start Date*: 2013-11-13 | |||||||||||
Sponsor Name:Idenix Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase I/IIa Study Assessing Single and Multiple Doses of IDX21437 in Healthy and HCV-Infected Subjects | |||||||||||||
Medical condition: Hepatitis C virus | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001431-31 | Sponsor Protocol Number: AT-01B-002 | Start Date*: 2019-05-20 | |||||||||||
Sponsor Name:Atea Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2 Study Assessing the Safety and Efficacy of AT-527 in Combination with Daclatasvir in Subjects with Chronic HCV Infection | |||||||||||||
Medical condition: HCV-Infected subjects | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
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