- Trials with a EudraCT protocol (2,069)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
2,069 result(s) found for: Drug testing.
Displaying page 1 of 104.
EudraCT Number: 2021-003514-39 | Sponsor Protocol Number: GNCbumet | Start Date*: Information not available in EudraCT |
Sponsor Name:Gillberg Neuropsychiatry Centre | ||
Full Title: Testing E/I imbalance in autism with Bumetanide – a parallel group randomized waitlist-control trial in adolescents and adults | ||
Medical condition: Autism Spectrum Disorder | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001918-98 | Sponsor Protocol Number: 31052015 | Start Date*: 2016-01-12 |
Sponsor Name:Vestre Viken HF | ||
Full Title: RATe control in Atrial Fibrillation II | ||
Medical condition: Permanent atrial fibrillation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017828-54 | Sponsor Protocol Number: 1131/09 | Start Date*: 2011-03-28 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Cross-reactivity and tolerability of ertapenem in patients with IgE-mediated allergy to -lactams. | |||||||||||||
Medical condition: allergy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004996-35 | Sponsor Protocol Number: 2010CV30 | Start Date*: 2011-12-23 |
Sponsor Name:University of Dundee | ||
Full Title: Allopurinol as a possible new therapy for acute coronary syndromes: The Next Steps | ||
Medical condition: Acute coronary syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000865-13 | Sponsor Protocol Number: PMLD17102005 | Start Date*: 2006-04-17 |
Sponsor Name:Univ.Clinic of Dermatology | ||
Full Title: Evaluation of the impact from Polypodium leukotomos Extract on the Prophylaxis of Polymorphic Light Eruption (PMLE) An investigator initiated, prospective, open label study with an in Austria reg... | ||
Medical condition: Evaluation of the impact from Polypodium leukotomos Extract on the Prophylaxis of Polymorphic Light Eruption (PMLE) An investigator initiated, prospective, open label study with an in Austria reg... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-001396-16 | Sponsor Protocol Number: OP0595-6 | Start Date*: 2023-03-29 | |||||||||||||||||||||||||||||||
Sponsor Name:Meiji Seika Pharma Co., Ltd. | |||||||||||||||||||||||||||||||||
Full Title: A Phase 3, Multi-Center, Randomized, Single-Blind Study to Assess the Efficacy and Safety of Cefepime/Nacubactam and Aztreonam/Nacubactam Versus Best Available Therapy in Adults With Complicated Ur... | |||||||||||||||||||||||||||||||||
Medical condition: Complicated urinary tract infection (cUTI), acute uncomplicated pyelonephritis (AP), hospital acquired bacterial pneumonia (HABP), ventilator-associated bacterial pneumonia (VABP), and complicated ... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) SK (Trial now transitioned) GR (Trial now transitioned) LV (Trial now transitioned) ES (Ongoing) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000539-27 | Sponsor Protocol Number: CLAF237A2307 | Start Date*: 2004-09-08 |
Sponsor Name:Novartis Sverige AB | ||
Full Title: A Multicenter, Double-Blind, Randomized, Parallel-Group Study to Compare the Effect of 52 Weeks Treatment with LAF237 50 mg qd to Placebo in Drug-Naïve Patients with Type 2 Diabetes and Mild Hyperg... | ||
Medical condition: Type 2 Diabetes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) FI (Completed) ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-003766-41 | Sponsor Protocol Number: COVERAGE | Start Date*: 2020-09-16 |
Sponsor Name:Amsterdam UMC-AMC | ||
Full Title: The effect of Voxelotor on Cerebral Perfusion and Oxygenation (Coverage Study) | ||
Medical condition: Sickle Cell Disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000962-76 | Sponsor Protocol Number: 17992 | Start Date*: 2015-09-22 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: Single-dose study testing a rivaroxaban granules for oral suspension formulation in children from 2 months to 12 years with previous thrombosis | |||||||||||||
Medical condition: Thrombosis | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) BE (Completed) IE (Completed) ES (Completed) FI (Completed) HU (Completed) SE (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002275-28 | Sponsor Protocol Number: 1237.19 | Start Date*: 2014-11-18 | |||||||||||
Sponsor Name:Boehringer Ingelheim Finland Ky | |||||||||||||
Full Title: A randomised, double-blind, active-controlled parallel group study to evaluate the effect of 52 weeks of once daily treatment of orally inhaled tiotropium + olodaterol fixed dose combination compar... | |||||||||||||
Medical condition: chronic obstructive pulmonary disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) IT (Completed) SE (Completed) PT (Completed) DK (Completed) BE (Completed) NL (Completed) HU (Completed) GB (Completed) ES (Completed) AT (Completed) IE (Completed) LT (Completed) CZ (Completed) LV (Completed) SK (Completed) DE (Completed) SI (Completed) GR (Completed) BG (Completed) HR (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002262-37 | Sponsor Protocol Number: ATP1 | Start Date*: 2004-10-27 |
Sponsor Name:Newcastle Hospitals Trust | ||
Full Title: Adenosine testing in the diagnosis of unexplained syncope: A pilot study | ||
Medical condition: Syncope | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-004297-34 | Sponsor Protocol Number: 236252 | Start Date*: 2018-03-31 | |||||||||||
Sponsor Name:Aston University | |||||||||||||
Full Title: A placebo controlled double blind randomised controlled proof of concept study of zolpidem for the treatment of motor and cognitive deficits in late-stage Parkinson’s | |||||||||||||
Medical condition: Parkinson's Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002108-14 | Sponsor Protocol Number: PD-BLS-01-EU | Start Date*: 2005-06-22 |
Sponsor Name:Fresenius Medical Care Deutschland GmbH. | ||
Full Title: Multizentrische Studie mit einer Niedrig-Natrium Peritonealdialyse-Lösung bei hypertensiven od. antihypertensiv behandelten CAPD Patienten auf balance Lösung | ||
Medical condition: | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-001877-34 | Sponsor Protocol Number: HOT-Treated | Start Date*: 2016-11-25 | |||||||||||||||||||||
Sponsor Name:South London and Maudsley NHS Foundation Trust
[...]
1. South London and Maudsley NHS Foundation Trust
2. King's College London |
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Full Title: Improving understanding of Heroin Overdose Testing: diamorphine dose-escalation testing in a treated population | |||||||||||||||||||||||
Medical condition: Opioid Overdose | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004468-23 | Sponsor Protocol Number: version3.0 | Start Date*: 2020-02-10 |
Sponsor Name:St George's, University of London | ||
Full Title: Comparison of abatacept with tumor necrosis factor inhibitors in the treatment of rheumatoid arthritis pain: A phase IV trial | ||
Medical condition: Rheumatoid arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003119-21 | Sponsor Protocol Number: 1 | Start Date*: 2017-12-22 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Effect of Omalizumab in patients with Aspirin-Exazerbated Respiratory Disease (AERD) | ||
Medical condition: Aspirin-exacerbated respiratory disease (AERD), also known as Samter's triad or Widal's triad, comprises the triad of Asthma, chronic rhinosinusitis with nasal polyps (CRwNP) and nonsteroidal anti-... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000821-37 | Sponsor Protocol Number: GS-US-416-2124 | Start Date*: 2017-02-06 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Phase 2, Double-Blind, Randomized Study Evaluating the Safety, Tolerability, and Efficacy of GS-4997 in Combination with Prednisolone versus Prednisolone Alone in Subjects with Severe Alcoholic H... | |||||||||||||
Medical condition: Alcoholic Hepatitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) BE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005246-38 | Sponsor Protocol Number: 143660 | Start Date*: 2013-05-13 | |||||||||||
Sponsor Name:University of Oslo | |||||||||||||
Full Title: The effects of methylphenidate on brain processes for decision making in adult attention deficit hyperactivity disorder | |||||||||||||
Medical condition: Attention deficit hyperactivty disorder | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-005047-32 | Sponsor Protocol Number: H-100-002 | Start Date*: 2018-09-27 | |||||||||||
Sponsor Name:Hookipa Biotech GmbH | |||||||||||||
Full Title: A Randomized, Placebo-Controlled, Phase 2 Study of HB-101, a Bivalent Cytomegalovirus (CMV) Vaccine, in CMV-Seronegative Recipient (R-) Patients Awaiting Kidney Transplantation from Living CMV-Sero... | |||||||||||||
Medical condition: Prevention of clinically significant cytomegalovirus (CMV) infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) BE (Completed) FR (Completed) AT (Completed) NO (Completed) DE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002555-10 | Sponsor Protocol Number: DS1062-A-U304 | Start Date*: 2022-07-21 | |||||||||||
Sponsor Name:Daiichi Sankyo, Inc. | |||||||||||||
Full Title: A Randomized, Open-label, Phase 3 Trial of Dato-DXd Plus Pembrolizumab vs Pembrolizumab Alone in Treatment-naïve Subjects with Advanced or Metastatic PD-L1 High (TPS ≥50%) Non-small Cell Lung Cance... | |||||||||||||
Medical condition: Advanced or Metastatic Non-small Cell Lung Cancer (NSCLC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) DE (Trial now transitioned) NL (Trial now transitioned) GR (Trial now transitioned) PT (Trial now transitioned) HU (Trial now transitioned) PL (Trial now transitioned) BE (Trial now transitioned) AT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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