- Trials with a EudraCT protocol (80)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
80 result(s) found for: Eye Diseases AND Retinal Diseases AND ranibizumab.
Displaying page 1 of 4.
EudraCT Number: 2014-001047-21 | Sponsor Protocol Number: 690110 | Start Date*: 2014-06-09 |
Sponsor Name:Sankt Eriks Eye Hospital | ||
Full Title: Randomized trial comparing injection frequency between Aflibercept and Ranibizumab in patients with Central Retinal Vein Occlusion with a treat and extent algorithm | ||
Medical condition: Central retinal vein occlusion | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003352-20 | Sponsor Protocol Number: 469055 | Start Date*: 2016-07-18 | |||||||||||
Sponsor Name:University Medical Center of Johannes -Gutenberg University Mainz | |||||||||||||
Full Title: Correlation of functional and structural outcomes with serum antibody profiles in patients with neovascular age-related macular degeneration treated with ranibizumab and healthy subjects: a prospec... | |||||||||||||
Medical condition: Neovascular age-related macular degeneration (AMD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020441-27 | Sponsor Protocol Number: CORaLa | Start Date*: 2011-02-23 | ||||||||||||||||
Sponsor Name:University of Leipzig Ritterstr. 26, 04109 Leipzig | ||||||||||||||||||
Full Title: Ranibizumab combined with selective peripheral laser photocoagulation for treatment of central retinal vein occlusion A randomized, controlled interventional phase 2b (proof of concept) study of ... | ||||||||||||||||||
Medical condition: macular edema secondary to non-ischemic central retinal vein occlusion | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022616-39 | Sponsor Protocol Number: CRFB002DGB14 | Start Date*: 2010-11-30 |
Sponsor Name:Novartis Pharmaceuticals UK Ltd | ||
Full Title: RELIGHT - Ranibizumab treatment of diabetic macular oEdema with bimonthLy monItorinG after a pHase of initial Treatment. A UK, 18-month, prospective, open-label, multicenter, single-arm Phase IIIb ... | ||
Medical condition: Diabetic Macular Oedema | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-002859-34 | Sponsor Protocol Number: CRFB002E2402 | Start Date*: 2012-04-20 | |||||||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||||||||||||
Full Title: A 24-month, phase IIIb, open-label, randomized, activecontrolled, 3-arm, multicenter study assessing the efficacy and safety of an individualized, stabilization-criteria-driven PRN dosing regimen w... | |||||||||||||||||||||||
Medical condition: visual impairment due to macular edema secondary to branch retinal occlusion (BRVO) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IE (Completed) GB (Completed) SE (Completed) HU (Completed) CZ (Completed) ES (Completed) SK (Completed) GR (Completed) NL (Completed) PT (Completed) PL (Completed) FR (Completed) IT (Completed) DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-001970-41 | Sponsor Protocol Number: 0504-19 | Start Date*: 2022-03-18 | |||||||||||
Sponsor Name:Intas Pharmaceuticals Ltd. | |||||||||||||
Full Title: A Double Masked, Parallel Group, Randomized, Multicenter, Clinical Study to Compare Efficacy and Safety of Intas Ranibizumab with Lucentis® in Patients with Neovascular (Wet) Age-Related Macular De... | |||||||||||||
Medical condition: Neovascular (Wet) Age-Related Macular Degeneration (AMD) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) PL (Completed) LV (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001869-41 | Sponsor Protocol Number: OKHN1005 | Start Date*: 2011-08-24 | ||||||||||||||||
Sponsor Name:Moorfields Eye Hospital NHS Foundation Trust | ||||||||||||||||||
Full Title: An exploratory study of ranibizumab (Lucentis) for treatment of uveitic patients with refractory cystoid macular oedema. 'The LIMO study' | ||||||||||||||||||
Medical condition: Uveitic Macular Oedema | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-005439-10 | Sponsor Protocol Number: RabOCT | Start Date*: 2013-08-30 | ||||||||||||||||
Sponsor Name:University of Leipzig Ritterstr. 26, 04109 Leipzig | ||||||||||||||||||
Full Title: Re-treatment with intravitreal application of ranibizumab guided by morphological macular changes documented by optical coherence tomography (OCT) in patients with macular edema due to branch retin... | ||||||||||||||||||
Medical condition: macular edema secondary to branch retinal vein occlusion (BRVO) | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003041-10 | Sponsor Protocol Number: CRFB002H2301 | Start Date*: 2015-04-14 | |||||||||||
Sponsor Name:NOVARTIS FARMA S.p.A. | |||||||||||||
Full Title: RAINBOW study: a randomized, controlled study evaluating the efficacy and safety of RAnibizumab compared with laser therapy for the treatment of INfants BOrn prematurely With retinopathy of prematu... | |||||||||||||
Medical condition: Retinopathy of prematurity (ROP) | |||||||||||||
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Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) EE (Completed) LT (Completed) HU (Completed) BE (Completed) AT (Completed) DE (Completed) GB (Completed) HR (Completed) FR (Completed) SK (Completed) CZ (Completed) GR (Completed) DK (Completed) FI (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005418-20 | Sponsor Protocol Number: CRFB002G2302 | Start Date*: 2013-07-03 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: A 12-month, randomized, double-masked, sham-controlled, multicenter study to evaluate the efficacy and safety of 0.5 mg ranibizumab intravitreal injections in patients with visual impairment due ... | ||||||||||||||||||
Medical condition: Visual impairment due to vascular endothelial growth factor (VEGF) driven macular edema (ME) | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SK (Completed) IT (Completed) GB (Completed) LV (Completed) HU (Completed) CZ (Completed) IE (Completed) ES (Completed) BE (Completed) NL (Completed) DE (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-001020-38 | Sponsor Protocol Number: CRFB002EDE18 | Start Date*: 2011-06-24 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A 6-month multicenter, randomized, double-masked phase IIIb-study comparing the efficacy and safety of Lucentis (Ranibizumab) intravitreal injections versus Ozurdex (Dexamethasone) intravitreal imp... | |||||||||||||
Medical condition: visual impairment due to macular edema following central retinal vein occlusion (CRVO) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) HU (Completed) CZ (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006131-53 | Sponsor Protocol Number: AU-06104G | Start Date*: 2007-08-02 | |||||||||||
Sponsor Name:Society (institute) for clinical research | |||||||||||||
Full Title: Ranibizumab for Branch Retinal Vein Occlusion Associated Macular Edema Study | |||||||||||||
Medical condition: Macular edema secondary to branch retinal vein occlusion | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-000681-42 | Sponsor Protocol Number: CoRaLa_II | Start Date*: 2020-08-24 | ||||||||||||||||
Sponsor Name:Justus-Liebig University Gießen | ||||||||||||||||||
Full Title: Long-term need of ranibizumab injections with or without early targeted peripheral laser photocoagulation for treatment of macular edema due to central retinal vein occlusion | ||||||||||||||||||
Medical condition: Macular edema due to central retinal vein occlusion | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) AT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005417-38 | Sponsor Protocol Number: CRFB002G2301 | Start Date*: 2013-07-03 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: A 12-month, randomized, double-masked, sham-controlled, multicenter study to evaluate the efficacy and safety of 0.5mg ranibizumab intravitreal injections in patients with visual impairment due to ... | ||||||||||||||||||
Medical condition: Visual impairment due to vascular endothelial growth factor (VEGF) driven choroidal neovascularization (CNV) | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SK (Completed) IT (Completed) LV (Completed) PT (Completed) HU (Completed) CZ (Completed) ES (Completed) LT (Completed) BE (Completed) GR (Completed) DK (Completed) DE (Completed) PL (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-004736-24 | Sponsor Protocol Number: OPT-302-1004 | Start Date*: 2021-07-19 | |||||||||||||||||||||
Sponsor Name:Opthea Limited | |||||||||||||||||||||||
Full Title: A Phase 3, Multicentre, Double-masked, Randomised Study to Evaluate the Efficacy and Safety of Intravitreal OPT-302 in Combination with Ranibizumab, Compared with Ranibizumab Alone, in Participants... | |||||||||||||||||||||||
Medical condition: Neovascular age-related macular degeneration (wet AMD) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) CZ (Trial now transitioned) GR (Trial now transitioned) HU (Trial now transitioned) DK (Trial now transitioned) BG (Completed) PL (Trial now transitioned) ES (Ongoing) LV (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001019-30 | Sponsor Protocol Number: CRFB002EDE17 | Start Date*: 2011-06-01 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A 6-month multicenter, randomized, double-masked phase IIIb-study comparing the efficacy and safety of Lucentis (Ranibizumab) intravitreal injections versus Ozurdex (Dexamethasone) intravitreal imp... | |||||||||||||
Medical condition: visual impairment due to macular edema following branch retinal vein occlusion (BRVO) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) HU (Completed) CZ (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002790-11 | Sponsor Protocol Number: V4.0 | Start Date*: 2015-06-08 | ||||||||||||||||
Sponsor Name:Ludwig-Maximilians Universität München | ||||||||||||||||||
Full Title: Evaluation of additional peripheral panretinal LASER-treatment on recurrences of macular edema due to CRVO undergoing anti-VEGF treatment with ranibizumab | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-000487-11 | Sponsor Protocol Number: CRFB002D2201 | Start Date*: 2005-09-30 |
Sponsor Name:Novartis Pharma Service AG | ||
Full Title: A randomized, double-masked, multicenter, phase II study assessing the safety and efficacy of two concentrations of ranibizumab (intravitreal injections) compared with non-treatment control for the... | ||
Medical condition: Male and female patients >18 years of age with either type 1 or type 2 diabetes mellitus with stable HbA1c levels between 6.5 and 10% and diabetic macular edema with center involvement in at least ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) DK (Completed) GB (Completed) AT (Completed) ES (Completed) IT (Completed) PT (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-002350-31 | Sponsor Protocol Number: CRFB002E2401 | Start Date*: 2012-02-24 | |||||||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||||||||||||
Full Title: A 24-month, phase IIIb, open-label, single arm, multicenter study assessing the efficacy and safety of an individualized, stabilization criteria-driven PRN dosing regimen with 0.5-mg ranibizumab in... | |||||||||||||||||||||||
Medical condition: visual impairment due to macular edema secondary to central retinal vein occlusion (CRVO) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) IE (Completed) SE (Completed) HU (Completed) AT (Completed) ES (Completed) CZ (Completed) SK (Completed) GR (Completed) PT (Completed) NL (Completed) PL (Completed) IT (Completed) DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
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 |
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