- Trials with a EudraCT protocol (123)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
123 result(s) found for: Wet macular degeneration.
Displaying page 1 of 7.
EudraCT Number: 2010-021777-37 | Sponsor Protocol Number: Lucentis-LucERG | Start Date*: 2010-09-27 | |||||||||||
Sponsor Name:Universitätsklinikum Schleswig-Holstein (UK-SH) | |||||||||||||
Full Title: "A prospective, non-randomized, mono-center, cohort study to evaluate the short- and long-term effects of 0.5mg intraocular Ranibizumab (Lucentis) injections on retinal function in patients with we... | |||||||||||||
Medical condition: Retinal function in patients with wet age-related macular degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004567-30 | Sponsor Protocol Number: 1313.20 | Start Date*: 2014-04-15 | |||||||||||
Sponsor Name:Boehringer Ingelheim RCV GmbH & Co KG | |||||||||||||
Full Title: A single arm open label study to evaluate the pharmacodynamics and safety of a 4 wk treatment with BI 144807 in patients with newly diagnosed wet age related macular degeneration (wAMD) | |||||||||||||
Medical condition: patients with newly diagnosed, unilateral, wet Are-Related Macular Degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) DE (Prematurely Ended) AT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-018637-21 | Sponsor Protocol Number: 1 | Start Date*: 2013-11-20 | ||||||||||||||||
Sponsor Name:Universitätsklinikum Schleswig-Holstein UKSH | ||||||||||||||||||
Full Title: Intravitreal Injection of Lucentis (Ranibizumab) after Pars Plana Vitrectomy and Subretinal Application of Recombinant Tissue Plasminogen Activator (rtPA) in Patients with Acute Submacular Hemorrha... | ||||||||||||||||||
Medical condition: exsudative age-related macular degeneration with acut submacular hemorrhage | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005500-18 | Sponsor Protocol Number: VITCLEAR | Start Date*: 2013-11-18 | ||||||||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust [...] | ||||||||||||||||||
Full Title: A pharmacokinetic study: ranibizumab, aflibercept and the effect of vitrectomy | ||||||||||||||||||
Medical condition: Age-related macular degeneration | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-012509-20 | Sponsor Protocol Number: MERLOT | Start Date*: 2009-07-28 | |||||||||||
Sponsor Name:King's College Hospital NHS Foundation Trust | |||||||||||||
Full Title: A randomised controlled trial of epimacular brachytherapy versus ranibizumab monotherapy for the treatment of subfoveal choroidal neovascularisation associated with wet age-related macular degenera... | |||||||||||||
Medical condition: Wet age-related macular degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-005091-17 | Sponsor Protocol Number: 26285/13 | Start Date*: 2014-02-05 | |||||||||||
Sponsor Name:POLICLINICO GEMELLI | |||||||||||||
Full Title: Variation of choroidal Thickness 15 days after the first ranibizumab intravitreal injection in naïve patients WIth Neovascular age-related macular degeneration: pilot Study. – | |||||||||||||
Medical condition: Wet age-related macular degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017435-18 | Sponsor Protocol Number: CLIN905 MLT202 | Start Date*: 2010-02-04 | ||||||||||||||||
Sponsor Name:Steba Biotech S.A. | ||||||||||||||||||
Full Title: A Phase IIa, Safety and Preliminary Effects Study of WST11 (Stakel®)-Mediated Vascular-Targeted Photodynamic (VTP) Therapy in Subjects with Choroidal Neovasularization (CNV) Associated with Age-Rel... | ||||||||||||||||||
Medical condition: Age associated Macular Degeneration | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000518-23 | Sponsor Protocol Number: OPH1007 | Start Date*: 2015-10-20 | ||||||||||||||||
Sponsor Name:OPHTHOTECH CORPORATION | ||||||||||||||||||
Full Title: A phase 2b randomized, double-masked, controlled trial to establish the safety and efficacy of intravitreous administration of Fovista® (Anti-PDGFBB pegylated aptamer) administered in combination w... | ||||||||||||||||||
Medical condition: Subfoveal neovascular age-related macular degeneration (AMD) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Prematurely Ended) EE (Prematurely Ended) CZ (Prematurely Ended) HR (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-003763-22 | Sponsor Protocol Number: BAY73-4506/15984 | Start Date*: 2014-07-02 | ||||||||||||||||||||||||||
Sponsor Name:Bayer HealthCare AG | ||||||||||||||||||||||||||||
Full Title: A combined Phase IIa / IIb study of the efficacy, safety, and tolerability of repeated topical doses of regorafenib eye drops, in treatment-naïve subjects with neovascular age related macular degen... | ||||||||||||||||||||||||||||
Medical condition: neovascular age related macular degeneration | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: HU (Prematurely Ended) DE (Prematurely Ended) CZ (Prematurely Ended) SK (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-004078-24 | Sponsor Protocol Number: TAPAS | Start Date*: 2013-01-24 | ||||||||||||||||
Sponsor Name:King's College London [...] | ||||||||||||||||||
Full Title: Intravitreal Tissue Plasminogen Activator (tPA), Perfluoropropane (C3F8), and Ranibizumab for Neovascular Age-Related Macular Degeneration and Submacular Haemorrhage (TAPAS): A Randomized, Double-M... | ||||||||||||||||||
Medical condition: Sub-macular haemorrhage secondary to wet macular degeneration | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015681-55 | Sponsor Protocol Number: C-09-023 | Start Date*: 2010-03-18 | ||||||||||||||||
Sponsor Name:Alcon Research, Ltd. | ||||||||||||||||||
Full Title: A Dose-Escalation Study of AL-39324 Suspension versus Lucentis™ for the Treatment of Exudative Age-Related Macular Degeneration | ||||||||||||||||||
Medical condition: Exudative Age-related macular degeneration | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) AT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002202-70 | Sponsor Protocol Number: | Start Date*: 2011-09-22 | |||||||||||
Sponsor Name:Universitätsklinikum Schleswig-Holstein (UK-SH) | |||||||||||||
Full Title: A prospective, non-randomized, mono-center, cohort study to evaluate the effects of 0.5mg intraocular Ranibizumab (Lucentis) injections on retinal function in patients with diabetic macular edema (... | |||||||||||||
Medical condition: Retinal function in patients with wet age-related macular degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002168-34 | Sponsor Protocol Number: FNB-OK-2013-01 | Start Date*: 2014-12-09 | |||||||||||||||||||||
Sponsor Name:Doc. MUDr. Petr Kolář, PhD, Oční klinika FN Brno | |||||||||||||||||||||||
Full Title: Study To Determine Efficacy of Aflibercept For Treatment Of Retinal Angiomatous Proliferation Secondary To Age Related Macular Degeneration | |||||||||||||||||||||||
Medical condition: Retinal angiomatous proliferation secondary to wet age related macular degeneration. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-024001-12 | Sponsor Protocol Number: LuMi-1 | Start Date*: 2011-01-27 | |||||||||||
Sponsor Name:TYKS | |||||||||||||
Full Title: The effect of bevacizumab treatment on reading ability in age related macular degeneration | |||||||||||||
Medical condition: Age related macular degeneration of the eye, wet form | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003018-42 | Sponsor Protocol Number: OPH1004 | Start Date*: 2014-10-10 | ||||||||||||||||
Sponsor Name:OPHTHOTECH CORPORATION | ||||||||||||||||||
Full Title: A phase 3 randomized, double-masked, controlled trial to establish the safety and efficacy of intravitreous administration of Fovista™ (Anti PDGF-B pegylated aptamer) administered in combination wi... | ||||||||||||||||||
Medical condition: Subfoveal neovascular age-related macular degeneration | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: PT (Prematurely Ended) ES (Prematurely Ended) FI (Completed) NO (Completed) DE (Prematurely Ended) EE (Prematurely Ended) LV (Prematurely Ended) SK (Prematurely Ended) IT (Completed) AT (Prematurely Ended) HU (Completed) HR (Prematurely Ended) CZ (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-006290-90 | Sponsor Protocol Number: AU-06102G | Start Date*: 2008-10-10 | |||||||||||
Sponsor Name:Society (Institute) for clinical research | |||||||||||||
Full Title: Subretinal Macugen for neovascular age-related macular degeneration (SUMANA) | |||||||||||||
Medical condition: Neovascular (exudative) age-related macular degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016158-42 | Sponsor Protocol Number: IT-04-1-8-09 | Start Date*: 2009-12-23 | |||||||||||
Sponsor Name:U.L.S.S. 16 | |||||||||||||
Full Title: Efficacy of intravitreal bevacizumab for exudative age-related macular degeneration. | |||||||||||||
Medical condition: Exudative age-related macular degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000379-41 | Sponsor Protocol Number: RLBUHT3407 | Start Date*: 2007-05-22 | |||||||||||
Sponsor Name:Royal Liverpool & Broadgreen University hospital | |||||||||||||
Full Title: Liverpool Avastin Dose Response and Retreatment Study | |||||||||||||
Medical condition: Exudative senile macular degeneration of the retina | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005290-30 | Sponsor Protocol Number: TCA-05-01 | Start Date*: 2006-10-18 | |||||||||||
Sponsor Name:Department of Ophthalmology, Semmelweis University | |||||||||||||
Full Title: A Non- randomized, Single-Center, Open Label Case Series Study of Intravitreal Triamcinolone Acetate Injections (IVTA) Used as Adjunctive to Verteporfin Photodynamic Therapy (PDT) in the Treatment ... | |||||||||||||
Medical condition: Age- related macular degeneration with predominantly classic subfoveal choroidal neovascularisation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018741-65 | Sponsor Protocol Number: OPH1001A | Start Date*: 2010-04-21 | ||||||||||||||||
Sponsor Name:OPHTHOTECH CORPORATION | ||||||||||||||||||
Full Title: A PHASE 2, RANDOMIZED, DOUBLE-MASKED, CONTROLLED TRIAL TO ESTABLISH THE SAFETY AND EFFICACY OF INTRAVITREOUS INJECTIONS OF E10030 (ANTI-PDGF PEGYLATED APTAMER) GIVEN IN COMBINATION WITH LUCENTIS® I... | ||||||||||||||||||
Medical condition: Subfoveal choroidal neovascularization secondary to age-related macular degeneration (AMD) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: LV (Completed) FR (Completed) BE (Completed) DE (Completed) ES (Completed) HU (Completed) IT (Completed) AT (Completed) | ||||||||||||||||||
Trial results: View results |
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