- Trials with a EudraCT protocol (3,808)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3,808 result(s) found for: Clinical pharmacy.
Displaying page 1 of 191.
EudraCT Number: 2021-003823-14 | Sponsor Protocol Number: CDCA-PK | Start Date*: 2021-11-16 |
Sponsor Name:Amsterdam UMC | ||
Full Title: Pharmacokinetic cross-over study of compounded chenodeoxycholic acid. | ||
Medical condition: CTXCT | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000899-16 | Sponsor Protocol Number: UMM022013TG | Start Date*: 2013-10-16 |
Sponsor Name:Department of Pharmacy Unversitätsmedizin Mainz | ||
Full Title: Investigation of pharmacokinetics of Linezolid and Meropenem in patients receiving continuous renal replacement therapy | ||
Medical condition: Sepsis and acute renal failure (ARF) are pathological entities that commonly co-exist in patients admitted to intensive care. Antibiotic dosing in septic patients with ARF can be complicated and ma... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002948-14 | Sponsor Protocol Number: SC-FET15 | Start Date*: 2015-09-22 |
Sponsor Name:PET Diagnosztikai Kft. | ||
Full Title: Application of a new radioligand F-18 FET, and its clinical benefit in the diagnosis of primary and secondary brain tumors | ||
Medical condition: Primary and secondary brain tumors | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-000654-67 | Sponsor Protocol Number: FM1 | Start Date*: 2005-04-12 |
Sponsor Name:Uppsala University/Uppsala County Council | ||
Full Title: Can patients with fibromyalgia be improved by subcutaneous injections of sterile water in tenderpoints? A randomised, controlled, tripple masked clinical trial | ||
Medical condition: Fibromyalgia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-001600-12 | Sponsor Protocol Number: F/2004/2. | Start Date*: 2004-09-20 |
Sponsor Name:OMNINVEST Kft. | ||
Full Title: Fluval AB Vaccine Serologic Clinical Trial | ||
Medical condition: Immunization of healthy people against influenza virus infections. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-002789-20 | Sponsor Protocol Number: F/2006/1. | Start Date*: 2006-09-12 |
Sponsor Name:Omninvest Ltd. | ||
Full Title: FluvalAB Influenza Vaccine Serologic Clinical Trial for 2006-2007 Influenza Season | ||
Medical condition: Immunization of healthy people against influenza virus infections. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-002705-23 | Sponsor Protocol Number: F/2005/1. | Start Date*: 2005-09-23 |
Sponsor Name:OMNINVEST Kft. | ||
Full Title: FluvalAB Influenza Vaccine Serologic Clinical Trial for 2005-2006 Influenza Season | ||
Medical condition: Immunization of healthy people against influenza virus infections. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-006602-24 | Sponsor Protocol Number: PNC-2007 | Start Date*: 2008-03-31 |
Sponsor Name:Department of Pediatrics, Medical and Health Science Center, University of Debrecen | ||
Full Title: Relative adrenal insufficiency in children with pneumonia and sepsis. Efficacy of i.v. prednisolon for prevention of complication of pneumonia. A prospective, parallel-group, randomised trial. | ||
Medical condition: Severe complications of bacterial pneumonia i.e. abscess formation, empyema and sepsis in children. Supposed concomittant andrenal insuficiency is also planned to investigate. | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-002192-40 | Sponsor Protocol Number: periodld001 | Start Date*: 2006-07-13 |
Sponsor Name:Zsolt Lohinai DMD PhD | ||
Full Title: New treatment of periodontitis by inhibition of lysine decarboxilase enzyme | ||
Medical condition: healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001694-23 | Sponsor Protocol Number: OOI/KEMB/2006-1 | Start Date*: 2006-08-21 |
Sponsor Name:National Institute of Oncology | ||
Full Title: Efficacy of cetuximab in locally advanced or metastatic adenoid cystic carcinoma. Phase II. | ||
Medical condition: Investigating the efficacy of cetuximab (Erbitux) in locally advanced or metastatic adenoid cystic carcinoma expressing EGFR. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-006099-39 | Sponsor Protocol Number: DE 0206 | Start Date*: 2006-12-14 |
Sponsor Name:Department of Endocrinology University of Debrecen Medical and Health Science Center | ||
Full Title: Anti-CD20 antitest alkalmazása súlyos, hagyományos kezelésekre nem reagáló endokrin orbitopátiában | ||
Medical condition: Endocrin ophthalmopathy (conventional therapy resistent). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001222-15 | Sponsor Protocol Number: 47955 | Start Date*: 2014-07-30 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Bioavailability of voriconazole in critically ill patients | ||
Medical condition: Suspected or prophylaxis of invasive aspergillosis. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000838-36 | Sponsor Protocol Number: PX104.1.7-201 | Start Date*: 2004-09-20 |
Sponsor Name:Pharmexa A/S | ||
Full Title: A Phase II trial evaluating the immunological and clinical efficay and safety of HER-2 Protein Autovac(TM) monotherapy in patients with metastatic breast cancer | ||
Medical condition: Female patients with histologically proven metastatic or locally advanced breast cancer who have HER-2 overexpression in the primary tumour and/or a metastatic lesion. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-001412-30 | Sponsor Protocol Number: HMR3647A/4020 | Start Date*: 2005-12-02 |
Sponsor Name:Laboratoire Aventis | ||
Full Title: An open-label, randomized, multicenter, clinical study to compare the effects of telithromycin, azithromycin and cefuroxime axetil on the penicillin or macrolide resistance of Streptococcus pneumon... | ||
Medical condition: Patients with acute exacerbation of chronic bronchitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-004535-72 | Sponsor Protocol Number: TEIC_HM_1 | Start Date*: 2014-01-17 |
Sponsor Name:Tallaght Hospital, Dublin 24, Ireland | ||
Full Title: A prospective, single-centre, cohort study to determine the pharmacokinetic and pharmacodynamic parameters of teicoplanin in adult patients with haematological malignancy. | ||
Medical condition: Suspected or confirmed Gram-positive infection in patients with haematological malignancy. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002112-26 | Sponsor Protocol Number: 139B7 | Start Date*: 2007-05-21 |
Sponsor Name:YORK Pharma GmbH | ||
Full Title: Open, single-arm phase-III study to investigate the percutaneous absorption of abafungin after topical dermal application of Abafungin cream 1.0 % (YORK Pharma GmbH) in 20 patients with tinea pedis... | ||
Medical condition: Tinea pedis interdigital | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
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 | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (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. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000558-60 | Sponsor Protocol Number: PX104.1.7-202 | Start Date*: 2005-06-02 |
Sponsor Name:Pharmexa A/S | ||
Full Title: A Phase II trial evaluating the immunological and clinical efficacy and safety of HER-2 Protein AutoVac(TM) and Stimulon® Adjuvant QS-21 monotherapy in patients with metastatic breast cancer | ||
Medical condition: Female patients with histologically proven metastatic or locally advanced breast cancer who have HER-2 overexpression in the primary tumour and/or a metastatic lesion. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-004934-26 | Sponsor Protocol Number: N/A | Start Date*: 2008-11-26 | ||||||||||||||||
Sponsor Name:UMCG | ||||||||||||||||||
Full Title: Pharmacokinetics and –dynamics of intrathecal baclofen therapy in patients with spasticity | ||||||||||||||||||
Medical condition: Spasticity of varying origin (i.e. MS, spinal cord injury), which doesn't respond on treatment with oral medication | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
