- Trials with a EudraCT protocol (44,380)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,380 result(s) found.
Displaying page 1,549 of 2,219.
| EudraCT Number: 2004-004512-23 | Sponsor Protocol Number: PKU-003 | Start Date*: 2005-05-22 | |||||||||||
| Sponsor Name:BioMarin Pharmaceutical Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of Phenoptin in Subjects with Phenylketonuria Who Have Elevated Phenylalanine Levels | |||||||||||||
| Medical condition: Phenylketonuria (PKU) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) GB (Completed) DE (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-003778-13 | Sponsor Protocol Number: PKU-007 | Start Date*: 2006-07-13 | |||||||||||
| Sponsor Name:BioMarin Pharmaceutical Inc | |||||||||||||
| Full Title: A Phase 2, Multicenter, Open-label Study to Evaluate the Safety and Efficacy of Phenoptin in Subjects with Hyperphenylalaninemia Due to Primary BH4 Deficiency | |||||||||||||
| Medical condition: Phenylketonuria (PKU) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-001439-37 | Sponsor Protocol Number: MACSevoPregabalin | Start Date*: 2019-09-16 |
| Sponsor Name:Medical University of Vienna, Department of Anaesthesia, General Critical Care and Pain Management | ||
| Full Title: The effect of pregabalin on the minimal alveolar concentration of sevoflurane | ||
| Medical condition: This study aims to investigate the effect of clinically used doses of Pregabalin on the minimum alveolar concentration of sevoflurane to provide more information to clinicians using this adjunctive... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-004513-41 | Sponsor Protocol Number: PKU-004 | Start Date*: 2005-10-25 | |||||||||||
| Sponsor Name:BioMarin Pharmaceutical Inc. | |||||||||||||
| Full Title: A Phase 3, Multicenter, Open-Label Extension Study of Phenoptin in Subjects with Phenylketonuria Who Have Elevated Phenylalanine Levels | |||||||||||||
| Medical condition: Phenylketonuria (PKU) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) IE (Completed) IT (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-002071-16 | Sponsor Protocol Number: PKU-001 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:BioMarin Pharmaceutical Inc. | |||||||||||||
| Full Title: A Phase 2, Multicenter, Open-Label Study to Evaluate the Response to and Safety of an 8-Day Course of Phenoptin Treatment in Subjects with Phenylketonuria Who Have Elevated Phenylalanine Levels | |||||||||||||
| Medical condition: Phenylketonuria (PKU) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Completed) DE (Completed) GB (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002165-19 | Sponsor Protocol Number: 20177308 | Start Date*: 2019-05-10 |
| Sponsor Name:Medical University Vienna | ||
| Full Title: Neo-BCC trial: Neoadjuvant treatment of difficult to resect, locally advanced basal cell carcinoma (BCC) with Talimogene laherparepvec (T-VEC) | ||
| Medical condition: Basal cell carcinoma (BCC) is the most common malignant neoplasm in fair skinned humans (Rubin et al., 2005). Over the last decades its incidence has increased (Chinem and Miot, 2011). Especially w... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-003195-39 | Sponsor Protocol Number: IM101-301 | Start Date*: 2013-08-26 | |||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
| Full Title: A Phase 3 Multi-center, Open-Label Study to Evaluate Pharmacokinetics, Efficacy and Safety of Abatacept Administered Subcutaneously (SC) in Children and Adolescents with Active Polyarticular Juveni... | |||||||||||||
| Medical condition: Active Polyarticular Juvenile Idiopathic Arthritis (pJIA) | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) ES (Completed) IT (Completed) Outside EU/EEA FR (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-001398-30 | Sponsor Protocol Number: MEDOPP437 | Start Date*: 2023-05-08 |
| Sponsor Name:Medica Scientia Innovation Research, S.L. | ||
| Full Title: PHASE II STUDY FOR PIK3CA/PTEN-ALTERED ADVANCED METAPLASTIC BREAST CANCER TREATED WITH MEN1611 MONOTHERAPY OR IN COMBINATION WITH ERIBULIN -THE SABINA STUDY- English PHASE II STUDY WITH MEN1611 M... | ||
| Medical condition: Hormone Receptor (HR)-known/ Human Epidermial Growth Factor Receptor 2 (HER2)-negative, phosphatidylinositol-4,5-bisphosphate 3kinase catalytic subunit alpha (PIK3CA)/ Phosphatase and Tensin Homolo... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-000079-38 | Sponsor Protocol Number: DB-OTO-001 | Start Date*: 2023-05-09 | |||||||||||
| Sponsor Name:Decibel Therapeutics | |||||||||||||
| Full Title: A Phase 1/2, Open-Label, Multicenter Trial With a Single Ascending Dose Cohort With Unilateral Intracochlear Injection Followed by a Bilateral Injection Expansion Cohort to Evaluate the Safety, Tol... | |||||||||||||
| Medical condition: Congenital auditory neuropathy secondary to biallelic mutations of the otoferlin gene (hOTOF) | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-001639-38 | Sponsor Protocol Number: GEMCAD-16-03 | Start Date*: 2017-07-19 | |||||||||||
| Sponsor Name:Grupo Español Multidisciplinar en Cáncer Digestivo (GEMCAD) | |||||||||||||
| Full Title: A phase II trial to evaluate the efficacy and safety of FOLFIRI + panitumumab as first-line treatment in elderly patients with RAS/BRAF wild-type unresectable metastatic colorectal cancer and good ... | |||||||||||||
| Medical condition: First-line treatment in elderly patients with RAS/BRAF wild-type unresectable metastatic colorectal cancer and good performance status | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005343-16 | Sponsor Protocol Number: 111344 | Start Date*: 2008-02-07 |
| Sponsor Name:GlaxoSmithKline Biologicals | ||
| Full Title: A phase II, open, study to assess the immunogenicity and reactogenicity of GlaxoSmithKline (GSK) Biologicals’ combined DTPa-HBV-IPV/Hib vaccine when administered as a booster dose to children aged ... | ||
| Medical condition: Booster immunisation of healthy toddlers in the second year of life against diphtheria, tetanus, pertussis, hepatitis B, polio and Haemophilus influenzae type b. | ||
| Disease: | ||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2020-003476-41 | Sponsor Protocol Number: ANB019-206 | Start Date*: 2021-07-17 | |||||||||||
| Sponsor Name:AnaptysBio Inc. | |||||||||||||
| Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of ANB019 in the Treatment of Subjects with Ichthyosis | |||||||||||||
| Medical condition: Ichthyosis | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002833-12 | Sponsor Protocol Number: GRAY-ZONE | Start Date*: 2020-01-27 | |||||||||||
| Sponsor Name:University Medical Centre Hamburg-Eppendorf | |||||||||||||
| Full Title: Investigator-initiated, placebo-controlled, randomized trial to assess the efficacy and safety of platelet inhibition and/ or lipid lowering in non-ACS-patients with elevated high-sensitivity tropo... | |||||||||||||
| Medical condition: Myocardial Ischemia | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-002352-36 | Sponsor Protocol Number: BO41929 | Start Date*: 2022-05-02 | |||||||||||
| Sponsor Name:F. Hoffmann La Roche Ltd. | |||||||||||||
| Full Title: A PHASE II, OPEN-LABEL, SINGLE-ARM DECENTRALIZED HOME-BASED APPROACH STUDY TO EVALUATE THE EFFICACY AND SAFETY OF ALECTINIB IN LOCALLY ADVANCED OR METASTATIC ALK-POSITIVE SOLID TUMORS | |||||||||||||
| Medical condition: Anaplastic lymphoma kinase (ALK)-positive solid tumors | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004065-25 | Sponsor Protocol Number: CCR4251 | Start Date*: 2015-07-28 |
| Sponsor Name:Royal Marsden | ||
| Full Title: Randomised Phase II Trial of Pembrolizumab and Radiotherapy in Melanoma | ||
| Medical condition: Advanced or unresectable melanoma. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-001196-10 | Sponsor Protocol Number: RC27022007 | Start Date*: 2007-09-18 | ||||||||||||||||
| Sponsor Name:Laboratoire BOIRON | ||||||||||||||||||
| Full Title: Etude d’évaluation de l’effet de Cuprum Metallicum 15 CH sur les crampes musculaires survenant en cours de dialyse chez des patients hémodialysés chroniques. Effect of Cuprum Metallicum 15 CH on m... | ||||||||||||||||||
| Medical condition: Crampes musculaires chez le patients hémodialysés chroniques. Muscle cramps happening at dialysis in chronic hemodialysed patients. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Ongoing) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2019-003182-17 | Sponsor Protocol Number: 1407-0004 | Start Date*: 2020-09-30 | |||||||||||
| Sponsor Name:Boehringer Ingelheim RCV GmbH & Co KG | |||||||||||||
| Full Title: A Phase II, randomised, double-blind, placebo-controlled, parallel-group, dose-ranging, proof-of-concept trial of BI 730357 given for 12 weeks in patients with active psoriatic arthritis | |||||||||||||
| Medical condition: psoriatic arthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Prematurely Ended) PL (Completed) BG (Completed) GB (GB - no longer in EU/EEA) CZ (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-000661-16 | Sponsor Protocol Number: CGRP2020 | Start Date*: 2020-06-18 | |||||||||||||||||||||
| Sponsor Name:Rigshospitalet Glostrup | |||||||||||||||||||||||
| Full Title: The effect of anti-calcitonin gene-related peptide (CGRP) receptor antibodies on the headache inducing properties of CGRP and cilostazol in migraine patients | |||||||||||||||||||||||
| Medical condition: Migraine | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2019-004628-39 | Sponsor Protocol Number: ABACUS-2 | Start Date*: 2020-12-16 | ||||||||||||||||
| Sponsor Name:Queen Mary University of London | ||||||||||||||||||
| Full Title: A phase II study of neoadjuvant immune checkpoint inhibitors in urothelial cancer | ||||||||||||||||||
| Medical condition: Tumours of the urothelial tract requiring surgery (T1 high grade-T4a of the bladder, rare histological subtypes) and upper urinary tract (high grade or high risk) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-003394-18 | Sponsor Protocol Number: PIPAC2trial | Start Date*: 2016-10-14 | |||||||||||
| Sponsor Name:Michael Bau Mortensen | |||||||||||||
| Full Title: Treatment of peritoneal carcinomatosis with Pressurized IntraPeritoneal Aerosol Chemotherapy - PIPAC-2 trial - | |||||||||||||
| Medical condition: Peritoneal carcinomatosis (PC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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