- Trials with a EudraCT protocol (171)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
171 result(s) found for: Neovascularization.
Displaying page 2 of 9.
EudraCT Number: 2014-003661-18 | Sponsor Protocol Number: 2014-878 | Start Date*: 2015-09-29 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Phase II study evaluating the efficacy of aflibercept for the treatment of choroidal neovascularization complicating angioid streaks in young subjects: the ASTRID study | |||||||||||||
Medical condition: choroidal neovascularization complicating angioid streaks | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002431-15 | Sponsor Protocol Number: CRFB002ADE23 | Start Date*: 2013-10-09 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A 12-month, phase IV, randomized, open label, multicenter study to compare efficacy of 0.5 mg ranibizumab PRN compared to 2 mg aflibercept bimonthly intravitreal injections on retinal thickness sta... | |||||||||||||
Medical condition: Visual impairment due to neovascular AMD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SE (Completed) NO (Completed) AT (Completed) DK (Completed) BE (Completed) NL (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003210-10 | Sponsor Protocol Number: B0451001 | Start Date*: 2009-09-24 | |||||||||||
Sponsor Name:Pfizer Inc., 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: PHASE II OPEN LABEL, MULTICENTER, PROSPECTIVE,RELATED MACULAR DEGENERATION, COMPARATOR STUDY EVALUATING PF-04523655 VERSUS RANIBIZUMAB TREATMENT OF SUBJECTS WITH CHOROIDAL NEOVASCULARIZATION (MONET... | |||||||||||||
Medical condition: Subfoveal Choroidal Neovascularization (CNV) associated with Age-related Macular Degeneration (AMD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) ES (Completed) BE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002626-23 | Sponsor Protocol Number: CRFB002A2411 | Start Date*: 2013-11-26 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: A 12-month, phase IIIb, randomized, visual acuity, assessor-masked, multicenter study assessing the efficacy and safety of ranibizumab 0.5mg in treat and extend regimen compared to monthly regimen,... | |||||||||||||
Medical condition: Visual impairment due to neovascular AMD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) BE (Completed) DE (Completed) SK (Completed) GB (Completed) HU (Completed) PT (Completed) DK (Completed) SI (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003640-23 | Sponsor Protocol Number: ECR-RET-2013-05 | Start Date*: 2014-01-13 | |||||||||||
Sponsor Name:AIBILI - Association for Innovation and Biomedical Research on Light and Image | |||||||||||||
Full Title: Prospective, randomized, multicentre, open label, phase II / III study to assess efficacy and safety of ranibizumab 0.5 mg intravitreal injections plus panretinal photocoagulation (PRP) versus PRP ... | |||||||||||||
Medical condition: Patients with type I or type II diabetes mellitus and high risk diabetic retinopathy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006785-15 | Sponsor Protocol Number: IOBA-02-2007 | Start Date*: 2008-03-10 | ||||||||||||||||
Sponsor Name:IOBA - Instituto Universitario de Oftalmobiología Aplicada | ||||||||||||||||||
Full Title: EFFICACY AND SECURITY OF INTRAVITREAL BEVACIZUMAB IN THE TREATMENT OF CHOROIDAL NEOVASCULAR MEMBRANES ASSOCIATED TO HIGH MYOPIA EVALUACIÓN DE LA EFICACIA Y SEGURIDAD DE LA INYECCIÓN INTRAVÍTREA D... | ||||||||||||||||||
Medical condition: Choroidal neovascular membrane in high myopia | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001182-27 | Sponsor Protocol Number: CRFB002ADE27 | Start Date*: 2014-08-27 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A randomized, single-blinded, multicenter, phase IV study to compare systemic VEGF protein dynamics following monthly intravitreal injections of 0.5 mg ranibizumab versus 2 mg aflibercept until stu... | |||||||||||||
Medical condition: Visual impairment due to neovascular AMD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000743-95 | Sponsor Protocol Number: CRFB002A2402 | Start Date*: 2007-08-08 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A phase IV, long-term, open-label, multicenter extension study to evaluate the safety and tolerability of ranibizumab in subjects with subfoveal choroidal neovascularization (CNV) secondary to age-... | ||
Medical condition: Study population will consist of patients with choroidal neovascularization (CNV) secondary to age-related macular degeneration (AMD) who received treatment in either of the two ongoing ranibizumab... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) BE (Completed) NL (Completed) DE (Completed) PT (Completed) ES (Completed) GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-003695-23 | Sponsor Protocol Number: 69HCL14-0201 | Start Date*: 2015-07-21 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: Phase II study evaluating the efficacy of aflibercept for the treatment of inflammatory choroidal neovascularization in young subjects: the ALINEA study | |||||||||||||
Medical condition: inflammatory choroidal neovascularization | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005601-22 | Sponsor Protocol Number: poc1doxy | Start Date*: 2008-03-27 | |||||||||||
Sponsor Name: | |||||||||||||
Full Title: Proof–of–concept study 1 (POC1): Evaluation of effect of doxycycline versus placebo on retinal function and posterior segment neovascularization in patients with severe non-proliferative or early ... | |||||||||||||
Medical condition: Diabetic retinopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004844-35 | Sponsor Protocol Number: TG-MV-005 | Start Date*: 2009-07-01 | |||||||||||||||||||||
Sponsor Name:ThromboGenics NV | |||||||||||||||||||||||
Full Title: A randomized, sham-injection controlled, double-masked, multicenter trial of microplasmin intravitreal injection for treatment of exudative age-related macular degeneration (AMD). | |||||||||||||||||||||||
Medical condition: Patients with exudative AMD with focal vitreomacular adhesion | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) GB (Completed) DE (Completed) IT (Completed) BE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-004416-31 | Sponsor Protocol Number: 206207-016 | Start Date*: 2008-03-07 |
Sponsor Name:Allergan Limited | ||
Full Title: A 6-Month, Single-Masked, Multicenter, Randomized, Controlled Study to Assess the Safety and Efficacy of 700 μg Dexamethasone Posterior Segment Drug Delivery System Applicator System as Adjunctive ... | ||
Medical condition: Choroidal neovascularization secondary to age-related macular degeneration | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PT (Completed) GB (Completed) IT (Completed) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002384-15 | Sponsor Protocol Number: 3.0 | Start Date*: 2014-10-23 | ||||||||||||||||||||||||||
Sponsor Name:Universitätsklinik für Augenheilkunde und Optometrie | ||||||||||||||||||||||||||||
Full Title: Intravitreal Aflibercept treatment in RAP-Lesions, PED, hemorrhagic CNV and PCV | ||||||||||||||||||||||||||||
Medical condition: Exsudative Maculopathies | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: AT (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-012941-45 | Sponsor Protocol Number: CRVO_LUC_09 | Start Date*: 2009-10-26 | |||||||||||||||||||||
Sponsor Name:Glostrup Hospital | |||||||||||||||||||||||
Full Title: LuRVO: Classification of Central Retinal Vein Occlusion and Management with Lucentis (Ranibizumab) - a randomised clinical trial. | |||||||||||||||||||||||
Medical condition: Central nethindeveneokklusion (e. central retinal vein occlusion, CRVO) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001085-10 | Sponsor Protocol Number: CRFB002AGB17 | Start Date*: 2014-09-08 | |||||||||||
Sponsor Name:Novartis Pharmaceuticals UK Ltd | |||||||||||||
Full Title: A phase IV, prospective, open label, uncontrolled, European study in patients with neovascular age-related macular degeneration (nAMD), evaluating the efficacy and safety of switching from intravit... | |||||||||||||
Medical condition: Visual impairment due to neovascular AMD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001856-36 | Sponsor Protocol Number: MEDICARE | Start Date*: 2013-08-05 | |||||||||||
Sponsor Name:CHU DE POITIERS | |||||||||||||
Full Title: Efficacy and safety of Aflibercept (Eylea®) in proliferative diabetic retinopathy | |||||||||||||
Medical condition: Percentage of patients showing regression of retinal neovascularization between baseline and month 12 in the Aflibercept group versus laser group | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021662-30 | Sponsor Protocol Number: CRFB002F2301 | Start Date*: 2010-11-05 | |||||||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||||||||||||
Full Title: A 12 month, phase III, randomized, double-masked, multi-center, active-controlled study to evaluate the efficacy and safety of two different dosing regimens of 0.5 mg ranibizumab vs. verteporfin PD... | |||||||||||||||||||||||
Medical condition: visual impairment due to choroidal neovascularization secondary to pathologic myopia | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PT (Completed) LV (Completed) HU (Completed) LT (Completed) FR (Completed) ES (Completed) IT (Completed) AT (Completed) SK (Completed) DE (Completed) GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-005388-33 | Sponsor Protocol Number: GS101-P3-CG | Start Date*: 2009-02-03 |
Sponsor Name:Les Laboratoires CTRS | ||
Full Title: A MULTICENTRE DOUBLE-BLIND RANDOMIZED STUDY TO INVESTIGATE THE EFFICACY AND TOLERABILITY OF GS-101 EYE DROPS, AN ANTISENSE OLIGONUCLEOTIDE, VERSUS PLACEBO ON INHIBITION OF CORNEAL NEOVASCULARIZATIO... | ||
Medical condition: Patients with corneal neovascularization, a major risk factor of corneal graft rejection. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) FR (Completed) | ||
Trial results: Removed from public view |
EudraCT Number: 2013-001421-55 | Sponsor Protocol Number: CRFB002GFR02 | Start Date*: 2013-06-13 | |||||||||||
Sponsor Name:Novartis Pharma S.A.S | |||||||||||||
Full Title: An open-label Extended Clinical Protocol of ranibizumab to evaluate Safety and Efficacy in rare VEGF driven ocular diseases. | |||||||||||||
Medical condition: Choroidal neovascularization not related to wet Age-related macular degeneration (wAMD), pathologic myopia (PM)or Pseudoxanthoma elasticum (PXE), as well as in Macular Edema (ME) not related to Ret... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-004867-31 | Sponsor Protocol Number: EOP 1012D | Start Date*: 2005-04-12 |
Sponsor Name:(OSI) Eyetech Pharmaceuticals, Inc | ||
Full Title: A Phase 3B/4, randomized, active controlled, double-masked, single dummy, multi-center comparative trial, in parallel groups, to compare the safety and efficacy of intravitreous injections of Macug... | ||
Medical condition: Exudative Age Related Macular Degeneration (AMD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) SE (Prematurely Ended) AT (Completed) DE (Prematurely Ended) IT (Completed) ES (Completed) | ||
Trial results: View results |
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