- Trials with a EudraCT protocol (2,211)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
2,211 result(s) found for: Drug development.
Displaying page 1 of 111.
EudraCT Number: 2019-001552-18 | Sponsor Protocol Number: A1481307 | Start Date*: 2019-07-26 | |||||||||||
Sponsor Name:Pfizer, Inc. | |||||||||||||
Full Title: A LOCAL, SINGLE-CENTRE, EXTENSION, OPEN LABEL ACCESS STUDY, TO PROVIDE SILDENAFIL THERAPY FOR SUBJECTS WHO COMPLETED A1481156 STUDY AND ARE JUDGED BY THE INVESTIGATOR TO DERIVE CLINICAL BENEFIT FRO... | |||||||||||||
Medical condition: pulmonary atrial hypertension | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002539-27 | Sponsor Protocol Number: IntraRenalTac | Start Date*: 2019-09-23 | |||||||||||
Sponsor Name:Oslo University Hospital – Rikshospitalet | |||||||||||||
Full Title: Association between intrarenal tacrolimus concentration and development of renal interstitial fibrosis in renal transplant recipients | |||||||||||||
Medical condition: Development of renal interstitial fibrosis in renal transplant recipients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002148-15 | Sponsor Protocol Number: 201500214815 | Start Date*: 2017-06-01 |
Sponsor Name:Bethesda Diabetes research Center (BDRC) | ||
Full Title: Pregnancy Outcomes: Effects of Metformin Study (POEM Study) a long term randomized controlled parallel group study in gestational diabetes mellitus | ||
Medical condition: Gestational diabetes mellitus | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-000780-24 | Sponsor Protocol Number: 9463-CL-2303 | Start Date*: 2012-07-24 |
Sponsor Name:Astellas Pharma Global Development, Inc. | ||
Full Title: A Phase 3, Randomized, Double-Blind, Multi-Center Study to Compare the Efficacy and Safety of Micafungin Versus Amphotericin B Deoxycholate for the Treatment of Neonatal Candidiasis | ||
Medical condition: Neonatal Candidiasis | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: GR (Completed) HU (Completed) BG (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001761-11 | Sponsor Protocol Number: 300488 | Start Date*: 2015-08-31 | ||||||||||||||||
Sponsor Name:The Department of Cardiothoracic and Vascular Surgery, Aarhus University Hospital | ||||||||||||||||||
Full Title: Lymphatic dysfunction as a cause of calcium channel blocker oedema in post-menopausal women | ||||||||||||||||||
Medical condition: Calcium channel antagonist induced peripheral edema in post-menopausal women. We hypothesize that this condition is partly due to impaired lymphatic function in these patients. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-005450-30 | Sponsor Protocol Number: ABI-MS-P01 | Start Date*: 2014-01-08 |
Sponsor Name:Medizinische Universität Innsbruck | ||
Full Title: Anti-Biopharmaceutical Immunization: Prediction and analysis of clinical relevance to minimize the risk of immunization in multiple sclerosis patients on interferon-beta treatment | ||
Medical condition: Development of neutralising antibodies against Interferon-beta in the treatment of multiple sclerosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001222-42 | Sponsor Protocol Number: CAPSS-272 | Start Date*: 2015-04-24 |
Sponsor Name:Johnson & Johnson Pharmaceutical Research and Development, L.L.C. | ||
Full Title: A double-blind trial comparing the efficacy, tolerability and safety of monotherapy topiramate versus phenytoin in subjects with seizures indicative of new onset epilepsy | ||
Medical condition: New onset epilepsy | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2011-005456-33 | Sponsor Protocol Number: | Start Date*: 2012-01-26 |
Sponsor Name:Med. Univ. Wien, Universitätsklinik für Kinder- und Jugendheilkunde | ||
Full Title: PREVENTING CHOLESTASIS IN PREMATURE INFANTS USING SMOFLIPID | ||
Medical condition: • To compare a mixed parenteral lipid emulsion containing fish oil (SMOFlipid®) with a soybean oil based lipid emulsion (Intralipid®) for its effect on the occurrence of parenteral nutrition associ... | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-004090-28 | Sponsor Protocol Number: Fx-R-001-S1/B3461049 | Start Date*: 2014-05-13 |
Sponsor Name:Fold RX Pharmaceuticals, a Pfizer Company | ||
Full Title: TRANSTHYRETIN-ASSOCIATED AMYLOIDOSES OUTCOMES SURVEY (THAOS) – OPTIONAL BLOOD SAMPLE COLLECTION SUBSTUDY | ||
Medical condition: Transthyretin (TTR) a 127-amino acid, tetrameric protein, primarily synthesized in the liver, is a secreted protein present in the blood and cerebrospinal fluid and is a carrier of thyroxine and r... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002258-60 | Sponsor Protocol Number: UMCN-ONCO-201302 | Start Date*: 2013-08-30 | |||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | |||||||||||||
Full Title: prediction of everolimus-induced interstitial lung disease in breast cancer patients; maximizing efficacy by reducing toxicity | |||||||||||||
Medical condition: breast cancer | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005772-35 | Sponsor Protocol Number: LINEZOLID01 | Start Date*: 2021-04-21 |
Sponsor Name:UCLouvain | ||
Full Title: Study on linezolid use and adverse drug reactions in clinical practice: Follow-up of patients treated in Belgian Hospitals | ||
Medical condition: All infections treated with the antibiotic linezolid | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
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: 2015-001223-23 | Sponsor Protocol Number: CAPSS-311 | Start Date*: 2015-04-24 |
Sponsor Name:Johnson & Johnson Pharmaceutical Research and Development, L.L.C. | ||
Full Title: TOPAMAX (Topiramate) Initiated as Monotherapy in Epilepsy (TIME): A Multicenter, Outpatient, Open-Label, Study to Evaluate the Dosing, Effectiveness and Safety of TOPAMAX as Monotherapy in the Trea... | ||
Medical condition: New onset epilepsy | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2004-002754-62 | Sponsor Protocol Number: 2004-001 | Start Date*: 2006-06-20 |
Sponsor Name:University of Göttingen; Dep. of Clinical Pharmacology | ||
Full Title: Development of CYP2D6 genotype based dosage guidelines for the beta-blockers metoprolol and carvedilol based on hepatic clearance and resting and exercise heart rate reduction | ||
Medical condition: Healthy male and female volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000788-27 | Sponsor Protocol Number: RD01273 | Start Date*: 2006-04-20 |
Sponsor Name:Royal United Hospital Bath NHS Trust | ||
Full Title: International Collaborative Infantile Spasms Study (ICISS) | ||
Medical condition: Infantile spasms are a rare severe form of epilepsy affecting approx 1 in 2,250 infants, usually under the age of 1 year. Affected infants have a very abnormal EEG and a poor prognosis for subseque... | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) | ||
Trial results: View results |
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: 2013-002084-26 | Sponsor Protocol Number: MK0991-064 | Start Date*: 2017-01-27 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp. | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Comparator-Controlled Study to Evaluate the Safety, Tolerability, and Efficacy of Caspofungin Versus Amphotericin B Deoxycholate in the Treatment of Invasiv... | |||||||||||||
Medical condition: Invasive Candidiasis | |||||||||||||
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Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Prematurely Ended) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001775-37 | Sponsor Protocol Number: MDGH-MOX-2001 | Start Date*: 2019-09-20 | |||||||||||
Sponsor Name:Medicines Development Limited (trading as Medicines Development for Global Health) | |||||||||||||
Full Title: A Phase II, randomized, double-blind, parallel group dose finding study of single oral doses of moxidectin in adults with scabies | |||||||||||||
Medical condition: Scabies (infection with Sarcoptes scabiei) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-002963-31 | Sponsor Protocol Number: D-CN-52014-243 | Start Date*: 2023-01-13 |
Sponsor Name:Ipsen Pharma | ||
Full Title: AN OPEN-LABEL, MULTICENTRE, SINGLE-ARM STUDY TO ASSESS THE EFFICACY AND SAFETY OF TRIPTORELIN 3-MONTH FORMULATION IN CHINESE CHILDREN WITH CENTRAL PRECOCIOUS PUBERTY | ||
Medical condition: Central Precocious Puberty | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2014-000605-12 | Sponsor Protocol Number: notapplicable1 | Start Date*: 2014-06-13 |
Sponsor Name: | ||
Full Title: Thiazide diuretics versus calcium channel blockers for the treatment of calcineurin inhibitor-induced hypertension in patients with psoriasis or eczema: a single-center randomized cross-over trial. | ||
Medical condition: Hypertension, induced by the use of a Calcineurin Inhibitor (CNI) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
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