- Trials with a EudraCT protocol (1,488)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (37)
1,488 result(s) found for: Pharmacodynamics.
Displaying page 1 of 75.
EudraCT Number: 2012-005443-24 | Sponsor Protocol Number: Dex-PKPD/01 | Start Date*: 2013-03-05 |
Sponsor Name:UMCG | ||
Full Title: Development of a pharmacokinetic/pharmacodynamic model of dexmedetomidine, and the effect of repeated auditory stimulation on pharmacodynamics of dexmedetomidine | ||
Medical condition: To develop a PKPD dexmedetomidine model, and to assess the effect of continuous auditory stimulation on dexmedetomidine pharmacodynamics. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004207-22 | Sponsor Protocol Number: CLCZ696B2319 | Start Date*: 2017-04-06 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: Multicenter, open-label, study to evaluate safety, tolerability, pharmacokinetics and, pharmacodynamics of LCZ696 followed by a 52-week randomized, double-blind, parallel group, active-controlled s... | |||||||||||||
Medical condition: Pediatric heart failure 1 month to <18 years old | |||||||||||||
|
|||||||||||||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) NL (Ongoing) SE (Completed) NO (Completed) ES (Completed) GB (GB - no longer in EU/EEA) CZ (Completed) IT (Completed) FR (Completed) BG (Completed) PL (Completed) HU (Completed) HR (Completed) AT (Completed) PT (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007647-14 | Sponsor Protocol Number: Nabu1A2 | Start Date*: 2009-01-07 |
Sponsor Name:Turku University Hospital | ||
Full Title: The effect of fluvoxamine and ciprofloxacin on the pharmacokinetics and pharmacodynamics of nabumetone: A three-phase double-blind placebo-controlled cross-over study. | ||
Medical condition: Pharmacokinetics and pharmacodynamics, healthy volunteer trial | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2023-000150-20 | Sponsor Protocol Number: 1 | Start Date*: 2023-03-22 |
Sponsor Name:Bispebjerg-Frederiksberg Hospital | ||
Full Title: The effect of exercise on pharmacodynamics and pharmacokinetics of a single dose of unfractionated heparin: A randomized, controlled, cross-over study | ||
Medical condition: Unfractionated heparin is used for the prevention and treatment of deep vein thrombosis and complications hereof | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-005200-13 | Sponsor Protocol Number: SafePed002 | Start Date*: 2015-07-09 |
Sponsor Name:Ghent University | ||
Full Title: study of the pharmacokinetics and pharmacodynamics of desmopressin oral lyophilisate - route of administration in the pediatric patient population - SAFEPEDRUG | ||
Medical condition: therapeutic population: monosympthomatic enuresis nocturna diagnostic population: children with a history of a urinary tract infection or suspicion of renal damage who need a renal concentration... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-000841-42 | Sponsor Protocol Number: RBHP2021GODET2 | Start Date*: 2021-04-28 |
Sponsor Name:CHU de CLERMONT-FERRAND | ||
Full Title: Cardiac Output Response to Vasopressine in major abdominal surgery patients under mechanical ventilation. A clinical pharmacodynamics study | ||
Medical condition: - | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-002803-15 | Sponsor Protocol Number: 12096 | Start Date*: 2006-08-18 | |||||||||||
Sponsor Name:Aarhus Sygehus | |||||||||||||
Full Title: Bioavailability, Pharmacokinetics and Pharmacodynamics of Insulin Aspart administered in the Duodenum in healthy volunteers – an open single blinded and uncontrolled exploratory trial | |||||||||||||
Medical condition: Diabetes Mellitus | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002353-29 | Sponsor Protocol Number: HUB-NEF-HEMOCIONA.EC | Start Date*: 2019-11-12 | ||||||||||||||||
Sponsor Name:HOSPITAL UNIVERSITARI DE BELLVITGE- IDIBELL | ||||||||||||||||||
Full Title: PHARMACOKINETICS, PHARMACODYNAMICS AND SAFETY OF APIXABAN IN PATIENTS IN HEMODAFILTRATION | ||||||||||||||||||
Medical condition: Chronic kidney disease, non-valvular atrial fibrillation | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000537-69 | Sponsor Protocol Number: PROP2% | Start Date*: 2015-09-21 |
Sponsor Name:Universitair Ziekenhuis Brussel | ||
Full Title: Real time monitoring of blood propofol concentration | ||
Medical condition: - General anaesthesia - Pharmacokinetics and Pharmacodynamics of Propofol - Inflammatory parameters - Elective thyroid, oncologic breast,ENT or cervical arthrodesis surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000808-40 | Sponsor Protocol Number: 2004-27-IMP-2 | Start Date*: 2005-01-13 |
Sponsor Name:Hexal AG | ||
Full Title: Randomized, open label, multi-center, phase III study on pharmacokinetics, pharmacodynamics, efficacy and safety of Goserelin 1M Implant HEXAL in patients with advanced prostatic cancer in comparis... | ||
Medical condition: Palliative treatment of advanced prostatic cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: LT (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-002873-62 | Sponsor Protocol Number: 2005-34-IMP-2 | Start Date*: 2006-02-15 |
Sponsor Name:HEXAL AG | ||
Full Title: RANDOMIZED, OPEN LABEL, MULTICENTER, PHASE II STUDY ON PHARMACOKINETICS, PHARMACODYNAMICS, EFFICACY AND SAFETY OF BUSERELIN 3M IMPLANT HEXAL IN PATIENTS WITH ADVANCED PROSTATIC CANCER IN COMPARISON... | ||
Medical condition: Palliative treatment of advanced prostatic cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-001279-36 | Sponsor Protocol Number: 2005-01-IMP-2 | Start Date*: 2005-08-24 |
Sponsor Name:Hexal AG | ||
Full Title: RANDOMIZED, OPEN LABEL, MULTICENTER, PHASE II STUDY ON PHARMACOKINETICS, PHARMACODYNAMICS, EFFICACY AND SAFETY OF GOSERELIN 3M IMPLANT HEXAL IN PATIENTS WITH ADVANCED PROSTATIC CANCER IN COMPARISON... | ||
Medical condition: Palliative treatment of advanced prostatic cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: LT (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-020204-30 | Sponsor Protocol Number: E5564-G000-103 | Start Date*: Information not available in EudraCT |
Sponsor Name:Eisai Limited [...] | ||
Full Title: A Multicenter, Open-label, Sequential, Multiple-dose Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety, Tolerability, and Efficacy or Eritoran in Descending Age Groups of Pediatric S... | ||
Medical condition: Severe Sepsis | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003004-31 | Sponsor Protocol Number: NP25139 | Start Date*: 2016-08-09 |
Sponsor Name:F. Hoffmann-La Roche AG | ||
Full Title: An Open Label, Prospective, Pharmacokinetic/Pharmacodynamic and Safety Evaluation of Intravenous Oseltamivir (Tamiflu) in the Treatment of Children 1 to 12 Years of Age With Influenza Infection | ||
Medical condition: Influenza | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2004-002701-68 | Sponsor Protocol Number: PSN9301CS01 | Start Date*: 2004-12-13 |
Sponsor Name:Prosidion Ltd. | ||
Full Title: A randomised, double-blind, placebo-controlled, multiple dose, time-lagged parallel groups trial, investigating the pharmacodynamics, the safety and tolerability and the pharmacokinetics of PSN9301... | ||
Medical condition: Diabetes mellitus type 2 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-002100-42 | Sponsor Protocol Number: ARD-0301-003 | Start Date*: 2005-08-24 |
Sponsor Name:Ardana Bioscience Ltd | ||
Full Title: A Phase II single centre, open-label study investigating the pharmacokinetics, pharmacodynamics, efficacy and safety of a loading dose regimen of a new GnRH antagonist, Teverelix, long-acting formu... | ||
Medical condition: advanced prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: LT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-001658-25 | Sponsor Protocol Number: A6391002 | Start Date*: 2005-06-16 |
Sponsor Name:Pfizer Global Research and Development | ||
Full Title: An open label, two period crossover study to explore the safety, pharmacokinetics and pharmacodynamics of PHA-794428 after single subcutaneous injections in adult male patients with growth hormone ... | ||
Medical condition: AGHD Adult Growth Hormone Deficiency | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-001988-23 | Sponsor Protocol Number: AEZS-130-P01 | Start Date*: 2018-11-07 | |||||||||||
Sponsor Name:Aeterna Zentaris GmbH | |||||||||||||
Full Title: Open label, group comparison, dose escalation trial to investigate safety, tolerability, pharmacokinetics and pharmacodynamics of macimorelin acetate after single oral dosing of 0.25 mg/kg, 0.5 mg/... | |||||||||||||
Medical condition: Diagnosis of Growth Hormone Deficiency | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-000427-20 | Sponsor Protocol Number: NL76691.100.22 | Start Date*: 2022-05-11 |
Sponsor Name:Inreda Diabetic | ||
Full Title: A stable glucagon analog administered by a bihormonal closed loop system; a feasibility study | ||
Medical condition: Type 1 Diabetes mellitus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2022-001373-31 | Sponsor Protocol Number: NL79588.091.22 | Start Date*: 2022-07-21 |
Sponsor Name:Inreda Diabetic B.V. | ||
Full Title: Fully Automated glycemic control with ultrarapid insulin in a bihormonal closed loop System in patients with Type 1 diabetes | ||
Medical condition: Type 1 diabetes mellitus | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
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. |
