- Trials with a EudraCT protocol (163)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
163 result(s) found for: Drug interactions.
Displaying page 1 of 9.
| EudraCT Number: 2021-003588-85 | Sponsor Protocol Number: PSYCHIC | Start Date*: 2022-01-11 |
| Sponsor Name:UCLouvain | ||
| Full Title: Individualized care with antipsychotics in patients suffering from schizophrenia spectrum disorders- How to conciliate plasma concentrations, clinical response and genetic factors ? | ||
| Medical condition: Schizophrenia, schizoaffective disorders, psychosis not otherwise specified, and dellusional disorders | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (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: 2012-000363-24 | Sponsor Protocol Number: Met-Dipy001 | Start Date*: 2012-04-18 | ||||||||||||||||
| Sponsor Name:Radboud University Medical Centre Nijmegen | ||||||||||||||||||
| Full Title: The effect of dipyridamole on the pharmacokinetics of metformin. | ||||||||||||||||||
| Medical condition: The antihyperglycemic drug metformin and the thrombocyte aggregation inhibitor dipyridamole are often used concomitantly in patients with diabetes who have suffered a transient ischemic attack or s... | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-000985-31 | Sponsor Protocol Number: RALAM-II | Start Date*: 2017-10-04 | |||||||||||
| Sponsor Name:Fundació Clinic per a la Recerca Biomédica | |||||||||||||
| Full Title: Phase 3b, single arm, single site simplification study with dual therapy including 3TC (300 mg QD) plus Raltegravir (1200 mg QD) in virologically suppressed HIV-1 infected atients experiencing inco... | |||||||||||||
| Medical condition: Virologically suppressed Human Immunodeficiency Virus-1 infected patients experiencing inconvenience, toxicity, negative impact on comorbidities or risk of drug-drug interactions with their current... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-014656-30 | Sponsor Protocol Number: CARDS Study | Start Date*: 2009-07-31 |
| Sponsor Name:AZIENDA OSPEDALIERA "OSPEDALI RIUNITI DI BERGAMO" (A.O. DI RILIEVO NAZIONALE) | ||
| Full Title: Combination of Atazanavir and Raltegravir as Dual Strategy | ||
| Medical condition: Documented HIV infection | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-001146-13 | Sponsor Protocol Number: A 001 | Start Date*: 2006-05-18 |
| Sponsor Name:University Hospital of Heidelberg | ||
| Full Title: "Investigation of Caspofungin Plasma Concentration and Pharmacokinetic for the Improvement of the Antifungal Therapy in Patients of Surgical Intensive Care Unit" | ||
| Medical condition: hospitalised patients | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-000469-62 | Sponsor Protocol Number: 2017-000469-62 | Start Date*: 2017-07-24 | ||||||||||||||||
| Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | ||||||||||||||||||
| Full Title: Pilot single‐arm clinical trial to evaluate the efficacy, PK interactions and safety of dolutegravir plus 2 NRTIs in HIV‐1‐infected solid organ transplant patients | ||||||||||||||||||
| Medical condition: HIV-1 infected solid organ transplant patients | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (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: 2022-000082-41 | Sponsor Protocol Number: 2021-0486 | Start Date*: 2022-03-31 |
| Sponsor Name:Fundación para la Investigación en Urología | ||
| Full Title: Impact of pitavastatin use in prostate cancer patients treated with new generation androgen therapy: multicenter clinical trial | ||
| Medical condition: We propose a multicenter, prospective, randomized, single-blind clinical trial, without conflict of interest, to determine the clinical benefit of statins (Pitavastatin 2 mg) in prostate cancer pa... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-002843-81 | Sponsor Protocol Number: 057 | Start Date*: 2020-01-07 |
| Sponsor Name:IMEA | ||
| Full Title: Switch to Tenofovir Alafenamide (TAF), Emtricitabine (FTC), Bictegravir (BIC)(Biktarvy®) in HIV-1-infected patients over 65 years old at risk of polymedication | ||
| Medical condition: HIV-1-infected patient Age > 65 years old Plasma HIV RNA ≤ 50 copies/mL for ≥ 6 months: one blip between 50 et 200 cp/ml is allowed in the last 6 months before screening. Currently receiving an ant... | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001070-29 | Sponsor Protocol Number: CRF005 | Start Date*: 2023-05-26 | |||||||||||
| Sponsor Name:Chelsea and Westminster NHS Foundation Trust | |||||||||||||
| Full Title: Efficacy, tolerability and acceptability of the single tablet regimen (STR) Biktarvy® by trans people living with HIV (TPLWH) | |||||||||||||
| Medical condition: Human Immunodeficiency Virus (HIV) infection | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004044-28 | Sponsor Protocol Number: AKF-396 | Start Date*: 2020-12-18 | |||||||||||
| Sponsor Name:University of Southern Denmark | |||||||||||||
| Full Title: Flucloxacillin as an inducer of CYP-enzymes | |||||||||||||
| Medical condition: Healthy volunteers. (Flucloxacillin is used against infections caused by beta-lactamase-producing organisms) Testing for drug-drug interactions caused by flucloxacillin | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-005998-27 | Sponsor Protocol Number: AKF-398 | Start Date*: 2021-03-12 | |||||||||||
| Sponsor Name:University of Southern Denmark | |||||||||||||
| Full Title: Interleukin-6 inhibitors and drug-drug interactions in patients with Rheumatoid Arthritis. | |||||||||||||
| Medical condition: Rheumatoid arthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-003696-43 | Sponsor Protocol Number: KUN 2008-4198 | Start Date*: 2008-11-25 |
| Sponsor Name:KWF Kankerbestrijding | ||
| Full Title: Prevention of progression of duodenal adenomas to cancer in patients with familial adenomatous polyposis | ||
| Medical condition: Familial Adenomatous Polyposis Duodenal adenomas and carcinomas | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-004049-29 | Sponsor Protocol Number: ISSBRIL0264 | Start Date*: 2015-03-10 |
| Sponsor Name:University of Leicester | ||
| Full Title: Investigating Aspirin and Ticagrelor for the prevention of tumour cell-induced platelet aggregation | ||
| Medical condition: Solid cancer metastasis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| 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: 2008-001881-10 | Sponsor Protocol Number: RAPHAEL study | Start Date*: 2008-05-27 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA "OSPEDALI RIUNITI DI BERGAMO" (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
| Full Title: Raltegravir/Atazanavir pharmacokinetics and evaluation of lipids | |||||||||||||
| Medical condition: chronic HIV infection | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-004686-34 | Sponsor Protocol Number: Evaluation Statin Therapy | Start Date*: 2007-02-27 | |||||||||||
| Sponsor Name:Karolinska University Hospital | |||||||||||||
| Full Title: Evaluation of Statin Therapy- Safety, Effect and Toxicity Mechanisms. | |||||||||||||
| Medical condition: Frequency of side effects in patients treated with HMG CoA reductase inhibitors. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-005381-19 | Sponsor Protocol Number: KIT-302-03-01 | Start Date*: 2014-05-16 | |||||||||||
| Sponsor Name:Kitov Pharmaceuticals Ltd | |||||||||||||
| Full Title: A Prospective Randomized Placebo Controlled Study to Evaluate the Effect of Celecoxib on the Efficacy and Safety of Amlodipine in Subjects with Hypertension Requiring Antihypertensive Therapy | |||||||||||||
| Medical condition: Hypertension | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-000766-12 | Sponsor Protocol Number: SCO/BIA-2093-301 | Start Date*: 2005-03-21 |
| Sponsor Name:BIAL Portela & Companhia, S.A. | ||
| Full Title: Efficacy and safety of BIA 2-093 as adjunctive therapy for refractory partial seizures in a double-blind, randomised, placebo-controlled, parallel-group, multicentre clinical trial | ||
| Medical condition: About 40% of the patients suffering from epilepsy are not satisfactorily controlled and 25% suffer from significant adverse events. This lack of seizure control means that combination therapy is of... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
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