- Trials with a EudraCT protocol (193)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
193 result(s) found for: AMD AND Age-Related Macular Degeneration.
Displaying page 2 of 10.
| 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: 2013-003333-15 | Sponsor Protocol Number: CRFB002AIT02 | Start Date*: 2013-11-15 | |||||||||||
| Sponsor Name:NOVARTIS FARMA | |||||||||||||
| Full Title: A 12 months, prospective, multicenter, open-label, single arm interventional study assessing the safety and tolerability of 0.5 mg ranibizumab in mono/bilateral wet AMD patients in eyes with BCVA b... | |||||||||||||
| Medical condition: Mono/bilateral Wet Age related Macular Degeneration (wAMD) in eyes with Best Corrected Visual Acuity (BCVA) below 2/10 and/or second affected eye . | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-003204-12 | Sponsor Protocol Number: ICI21/00025 | Start Date*: 2022-03-16 | |||||||||||
| Sponsor Name:Consorcio PSMAR | |||||||||||||
| Full Title: Multicentre, randomised, double-blind, parallel-group, Phase III study to evaluate the genetic polymorphisms influence in the response to Ranibizumab and Bevacizumab treatment in patients with Age-... | |||||||||||||
| Medical condition: age-related macular degeneration | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-004292-35 | Sponsor Protocol Number: 06NB37 | Start Date*: 2007-03-08 | |||||||||||
| Sponsor Name:Kings College Hospital NHS Foundation Trust | |||||||||||||
| Full Title: A pillot study to examine the safety and efficacy of intravitreal ranubizimab/dexamethasone administration and oral minocycline in addition to Visudyne (verteporfin) photdynamic therapy for subfove... | |||||||||||||
| 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: 2007-004721-23 | Sponsor Protocol Number: VIBERA | Start Date*: 2007-11-14 | |||||||||||
| Sponsor Name:Klinikum Bremen-Mitte gGmbH | |||||||||||||
| Full Title: Prevention of vision loss in patients with age-related neovascular macular degeneration by intravitreal injection of bevacizumab and ranibizumab in a typical outpatient setting | |||||||||||||
| Medical condition: age-related neovascular macular degeneration | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004523-16 | Sponsor Protocol Number: GR42691 | Start Date*: 2021-04-12 | |||||||||||
| Sponsor Name:F.Hoffmann La-Roche Ltd | |||||||||||||
| Full Title: A MULTICENTER, OPEN-LABEL EXTENSION STUDY TO EVALUATE THE LONG-TERM SAFETY AND TOLERABILITY OF FARICIMAB IN PATIENTS WITH NEOVASCULAR AGE-RELATED MACULAR DEGENERATION | |||||||||||||
| Medical condition: Neovascular age-related macular degeneration (nAMD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) PT (Completed) DE (Completed) AT (Completed) DK (Completed) HU (Completed) PL (Completed) NL (Completed) IT (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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: 2006-006358-86 | Sponsor Protocol Number: ATG003-201 | Start Date*: 2007-04-27 | |||||||||||
| Sponsor Name:CoMentis, Inc., USA | |||||||||||||
| Full Title: A PHASE II RANDOMIZED, DOUBLE-MASKED, STUDY COMPARING THE SAFETY AND EFFICACY OF ATG003 (MECAMYLAMINE HCL) 1.0% and 0.3% OPHTHALMIC SOLUTIONS TO PLACEBO IN PATIENTS WITH NEOVASCULAR ("WET") AGE-REL... | |||||||||||||
| Medical condition: Neovascular ("wet") Age-related Macular Degeneration (NV- AMD) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-003042-15 | Sponsor Protocol Number: ACU301 | Start Date*: 2007-10-12 | |||||||||||
| Sponsor Name:Opko Health, Incorporated | |||||||||||||
| Full Title: A Phase 3, randomized, double-masked, parallel-assignment study of intravitreal bevasiranib sodium, administered every 8 or 12 weeks as maintenance therapy following three injections of Lucentis® c... | |||||||||||||
| Medical condition: Patients with subfoveal choroidal neovascularization associated with Age-Related Macular Degeneration | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PT (Prematurely Ended) ES (Completed) AT (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| 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: 2006-003261-14 | Sponsor Protocol Number: R01 | Start Date*: 2006-08-28 | |||||||||||
| Sponsor Name:Retinaklinikken Omnia | |||||||||||||
| Full Title: A randomized pilot study comparing the safety and efficacy of intravireal triamcinolone acetonide given 7 days prior to or after Photodynamic therapy with Visudyne in patients with subfoveal choroi... | |||||||||||||
| Medical condition: Patients with age-related macular degeneration | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-004608-78 | Sponsor Protocol Number: LSFG-1.2 | Start Date*: 2017-03-03 | |||||||||||
| Sponsor Name:Kepler University Hospital, Institute of Ophthalmology | |||||||||||||
| Full Title: The Effect of Intravitreal Aflibercept on Ocular Perfusion – a Pilot Study | |||||||||||||
| Medical condition: Exudative AMD | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 2007-005607-18 | Sponsor Protocol Number: OPHT-011007 | Start Date*: 2009-04-02 | ||||||||||||||||
| Sponsor Name:Ursapharm Arzneimittel GmbH & Co KG | ||||||||||||||||||
| Full Title: An open study comparing the effects of moxaverine on ocular blood flow in patients with age- related macular degeneration, primary open angle glaucoma and healthy control subjects | ||||||||||||||||||
| Medical condition: glaucoma age-related macular degeneration | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: AT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2007-004487-53 | Sponsor Protocol Number: 2312/2007 | Start Date*: 2007-12-13 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA PISANA | |||||||||||||
| Full Title: Pilot study of association of VEGF polymorphisms with clinical efficacy and tolerability of therapy in patients affected by exudative (neovascular) age-related macular degeneration. | |||||||||||||
| Medical condition: Exudative and atrophic 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: 2005-006014-18 | Sponsor Protocol Number: 1419 | Start Date*: 2005-12-15 | |||||||||||
| Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
| Full Title: Macular structure and function after intravitreal injection of bevacizumab for wet macular degeneration a interventional study. | |||||||||||||
| Medical condition: Macular degeneration | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-017324-11 | Sponsor Protocol Number: CRFB002ADE09T | Start Date*: 2010-03-08 | |||||||||||
| Sponsor Name:Universitätsmedizin Göttingen | |||||||||||||
| Full Title: Wirksamkeit von Ranibizumab bei Patienten mit CHORIOIDALER NEOVASKULARISATION (CNV), als Folge einer altersbedingten Makuladegeneration (AMD), bei einer Gabe alle zwei Monate gegenüber der Behandlu... | |||||||||||||
| Medical condition: In der vorliegenden Studie wird in beiden Studienarmen Ranibizumab injiziert, es gibt keine Sham Gruppe. Randomisiert wird das Muster der Injektion (fixe Injektion alle 2 Monate versus Injektion be... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| 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: 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: 2011-000536-28 | Sponsor Protocol Number: C-10-083 | Start Date*: 2011-09-12 | |||||||||||
| Sponsor Name:Alcon Research Ltd. | |||||||||||||
| Full Title: Safety and efficacy study with ESBA1008 versus Lucentis for the treatment of exudative age-related macular degeneration | |||||||||||||
| Medical condition: wet 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 | |||||||||||||
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