- Trials with a EudraCT protocol (14)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
14 result(s) found for: Protective factor.
Displaying page 1 of 1.
EudraCT Number: 2014-005401-20 | Sponsor Protocol Number: CSLCT-BIO-03-97 | Start Date*: 2015-01-30 | |||||||||||
Sponsor Name:CSL Limited | |||||||||||||
Full Title: An Open-label, Multi-centre Study to Assess the Efficacy and Safety of Biostate® in Patients With von Willebrand's Disease (VWD) | |||||||||||||
Medical condition: Von Willebrand's disease (VWD) | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000441-58 | Sponsor Protocol Number: 08005DM-A | Start Date*: 2009-01-22 |
Sponsor Name:Belfast City Hospital | ||
Full Title: Investigation of the protective effects of keratinocyte growth factor (KGF) in a human lipopolysaccharide induced model of acute lung injury | ||
Medical condition: Acute lung injury | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-018531-17 | Sponsor Protocol Number: TRED012010 | Start Date*: 2010-06-25 |
Sponsor Name:Central Manchester University Hospitals NHS Foundation Trust | ||
Full Title: Effect of Tredaptive on serum lipoproteins, lipoproteins metabolism, oxidative stress and HDL antioxidant function. | ||
Medical condition: Hypercholesterolaemia. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-004042-42 | Sponsor Protocol Number: DEER | Start Date*: 2014-06-19 | ||||||||||||||||
Sponsor Name:King’s College London [...] | ||||||||||||||||||
Full Title: A study to investigate the potential renoprotective role of sodium-glucose transporter-2 (SGLT-2) antagonist Dapagliflozin in Type 2 diabetic patients with diabetic nephropathy | ||||||||||||||||||
Medical condition: Diabetic Nephropathy | ||||||||||||||||||
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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: 2021-000565-32 | Sponsor Protocol Number: PRIDE | Start Date*: 2023-04-27 | |||||||||||
Sponsor Name:Klinikum der Universität München | |||||||||||||
Full Title: PRIDE: A phase II a, open-label, multicenter study of radiochemotherapy with isotoxic dose escalation and protective VEGF inhibition using bevacizumab in the treatment of patients with first diagno... | |||||||||||||
Medical condition: Glioblastoma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001103-31 | Sponsor Protocol Number: AIT02-2001/DMID14-005 | Start Date*: 2015-07-10 | |||||||||||
Sponsor Name:Autoimmune Technologies, LLC | |||||||||||||
Full Title: A Phase 2a, Randomized, Double-blind, Placebo-controlled Assessment of the Safety and Protective Efficacy of FF-3 Dry Powder Administered by Nasal Inhalation for 5 Days to Healthy Adult Subjects wh... | |||||||||||||
Medical condition: Influenza A infection | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016731-34 | Sponsor Protocol Number: CRO1413 | Start Date*: 2010-01-08 | |||||||||||
Sponsor Name:Imperial College | |||||||||||||
Full Title: Amino acid regimen and intravenous lipid composition in preterm parenteral nutrition: a randomised double blind controlled trial of Nutritional Evaluation and Optimisation in Neonates. | |||||||||||||
Medical condition: Preterm birth | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021015-16 | Sponsor Protocol Number: TFM-CL3-002 | Start Date*: 2010-09-30 | |||||||||||
Sponsor Name:Olympus France SAS | |||||||||||||
Full Title: A Phase III, Double-Blind, Placebo Controlled, Parallel Group, International, Multicenter Study of 12 Weeks Treatment with Trafermin 0.01% Spray in Patients with Diabetic Foot Ulcer of Neuropathic ... | |||||||||||||
Medical condition: Wound closure rate of diabetic foot ulcers (DFUs) of neuropathic origin. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) BE (Completed) DK (Completed) SE (Completed) DE (Completed) NL (Completed) HU (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011175-70 | Sponsor Protocol Number: 805 | Start Date*: 2009-05-28 | |||||||||||||||||||||
Sponsor Name:Liverpool Heart and Chest Hospital | |||||||||||||||||||||||
Full Title: A randomised factorial trial of N-acetylcysteine prophylaxis and iso-osmolar versus low-osmolar contrast media on kidney function in patients at risk of contrast induced nephropathy following cardi... | |||||||||||||||||||||||
Medical condition: Contrast-induced nephropathy following cardiac catheterisation | |||||||||||||||||||||||
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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: 2017-000946-24 | Sponsor Protocol Number: 15-EI-0202 | Start Date*: 2018-01-09 |
Sponsor Name:National Eye Institute | ||
Full Title: Evaluation of Oral Minocycline in the Treatment of Geographic Atrophy Associated with Age-Related Macular Degeneration | ||
Medical condition: Geographic Atrophy Associated with Age-Related Macular Degeneration | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021014-33 | Sponsor Protocol Number: TFM-CL3-001 | Start Date*: 2010-09-30 | |||||||||||
Sponsor Name:Olympus France SAS | |||||||||||||
Full Title: A Phase III, Double-Blind, Placebo Controlled, Parallel Group, International, Multicenter Study of 12 Weeks Treatment with Trafermin 0.01% Spray in Patients with Diabetic Foot Ulcer of Neuropathic ... | |||||||||||||
Medical condition: Wound closure rate of diabetic foot ulcers (DFUs) of neuropathic origin. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002690-35 | Sponsor Protocol Number: OEV123 | Start Date*: 2017-05-08 | ||||||||||||||||
Sponsor Name:Scandinavian Biopharma AB | ||||||||||||||||||
Full Title: A randomized, placebo-controlled phase IIb (OEV 123) study to evaluate safety, immunogenicity, diagnostic methodology, and estimate vaccine efficacy of an oral enterotoxigenic Escherichia coli (ET... | ||||||||||||||||||
Medical condition: Healthy voluteers (prevention of diarrheal disease due to infection with enterotoxigenic E. coli [ETEC]) | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-004366-18 | Sponsor Protocol Number: CNTO148UCO1001 | Start Date*: 2013-07-30 | |||||||||||
Sponsor Name:Janssen Biologics B.V. | |||||||||||||
Full Title: A Phase 1b Open-Label Study to Assess the Safety and Pharmacokinetics of Subcutaneously Administered Golimumab, a Human anti-TNFα Antibody, in Pediatric Subjects with Moderately to Severely Active ... | |||||||||||||
Medical condition: Ulcerative Colitis in pediatric subjects | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) BE (Completed) DE (Completed) NL (Ongoing) DK (Completed) FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000962-14 | Sponsor Protocol Number: CCM-RNT-202101 | Start Date*: 2021-07-02 | |||||||||||
Sponsor Name:Charité - Universitätsmedizin Berlin | |||||||||||||
Full Title: A Monocenter, Open Label Study to Evaluate the Safety and Efficacy of Daratumumab in Combination with Standard Background Therapy in Participants with Moderate to Severe Systemic Lupus Erythematosus | |||||||||||||
Medical condition: Systemic Lupus Erythematosus | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
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