- Trials with a EudraCT protocol (228)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
228 result(s) found for: Age-Related Macular Degeneration.
Displaying page 9 of 12.
EudraCT Number: 2019-003883-28 | Sponsor Protocol Number: SB15-3001 | Start Date*: 2020-05-28 | |||||||||||
Sponsor Name:Samsung Bioepis Co., Ltd. | |||||||||||||
Full Title: A Phase III Randomised, Double-masked, Parallel Group, Multicentre Study to Compare the Efficacy, Safety, Pharmacokinetics, and Immunogenicity between SB15 (proposed aflibercept biosimilar) and Eyl... | |||||||||||||
Medical condition: Neovascular age-related macular degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) CZ (Completed) HU (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001221-40 | Sponsor Protocol Number: 1336-0007 | Start Date*: 2019-05-06 | |||||||||||||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||||||||||||
Full Title: Safety, tolerability and pharmacodynamics of single rising intravitreal and multiple rising intravitreal doses of BI 836880 in patients with wAMD (open label, non-randomized, uncontrolled). | |||||||||||||||||||||||
Medical condition: wet age-related macular degeneration (wAMD) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-004427-16 | Sponsor Protocol Number: GR40549 | Start Date*: 2021-09-28 | |||||||||||
Sponsor Name:Roche Farma S. A. U. que realiza el ensayo en España y que actúa como representante F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A MULTICENTER, OPEN-LABEL EXTENSION STUDY TO EVALUATE THE LONG TERM SAFETY AND TOLERABILITY OF THE PORT DELIVERY SYSTEM WITH RANIBIZUMAB IN PATIENTS WITH NEOVASCULAR AGE-RELATED MACULAR DEGENERATIO... | |||||||||||||
Medical condition: Neovascular Age-Related Macular Degeneration (nAMD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) DE (Trial now transitioned) BE (Trial now transitioned) FR (Trial now transitioned) AT (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002261-15 | Sponsor Protocol Number: ADVM-022-11 | Start Date*: 2023-03-23 | |||||||||||
Sponsor Name:Adverum Biotechnologies, Inc. | |||||||||||||
Full Title: A Multi-Center, Randomized, Double-Masked Phase 2 Study to Assess Safety and Efficacy of ADVM-022 (AAV.7m8-aflibercept) in Anti-VEGF Treatment- Experienced Patients with Neovascular (Wet) Age-relat... | |||||||||||||
Medical condition: Patients with Neovascular (Wet) Age-related Macular Degeneration (nAMD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
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: 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 |
EudraCT Number: 2019-002503-17 | Sponsor Protocol Number: 20170542 | Start Date*: 2020-08-10 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Randomized, Double-masked, Phase 3 Study of ABP 938 Efficacy and Safety Compared to Aflibercept (Eylea®) in Subjects with Neovascular Age-related Macular Degeneration | |||||||||||||
Medical condition: Neovascular Age-related Macular Degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LV (Completed) EE (Completed) SK (Completed) ES (Ongoing) CZ (Completed) LT (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004767-53 | Sponsor Protocol Number: CRTH258ADE01 | Start Date*: 2020-12-16 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A 52-week, two arm, randomized, open-label, multicenter study assessing the efficacy and safety of two different brolucizumab 6 mg dosing regimens for patients with suboptimal anatomically controll... | |||||||||||||
Medical condition: neovascular age-related macular degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003133-42 | Sponsor Protocol Number: 1672_2019 | Start Date*: 2020-02-14 |
Sponsor Name:Medical University of Vienna, Department of Ophthalmology and Optometry | ||
Full Title: Personalized treatment aided by automated analysis of fluid in active neovascular age-related macular degeneration (nAMD) in a prospective, multicenter, randomized study | ||
Medical condition: Nevoascular age related macular degneration (nAMD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003817-16 | Sponsor Protocol Number: KIN001-202 | Start Date*: 2019-04-04 | |||||||||||
Sponsor Name:Kinarus AG | |||||||||||||
Full Title: A 52 weeks double blind, randomized and placebo controlled trial evaluating the effect of oral KIN001 150 mg plus pioglitazone 10 mg daily on injection frequency of Standard of Care in patients wit... | |||||||||||||
Medical condition: wet age-related macular degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-002977-33 | Sponsor Protocol Number: Luc01AKSI | Start Date*: 2006-06-22 |
Sponsor Name:University Eye Hospital | ||
Full Title: Safety and efficacy of intravitreal injections of ranibizumab/Lucentis in combination with verteporfin photodynamic therapy (PDT) in patients with choroidal neovascularisation (CNV) secondary to ag... | ||
Medical condition: Age related macular degeneration (AMD) is the leading cause of blindness in individuals older than 50 years in the developed world. Eighty to ninety percent of rapid and severe vision loss due to A... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-000590-93 | Sponsor Protocol Number: CR213-20 | Start Date*: 2023-06-09 | |||||||||||
Sponsor Name:CuraTeQ Biologics Private Ltd. | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Parallel Group, Multicenter Study to Compare Efficacy, Safety, Pharmacokinetics, and Immunogenicity of BP05 Versus EU-Approved Lucentis® in Patients with Wet (N... | |||||||||||||
Medical condition: Wet (Neovascular) Age-Related Macular Degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Trial now transitioned) LV (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-004530-11 | Sponsor Protocol Number: ALT-L9-03 | Start Date*: 2022-04-21 | |||||||||||
Sponsor Name:Altos Biologics Inc. | |||||||||||||
Full Title: A Randomized, Phase 3, Double Masked, Parallel Group, Multicenter Study to Compare the Efficacy and Safety of ALT L9 Versus Eylea® in Patients With Neovascular Age Related Macular Degeneration (ALT... | |||||||||||||
Medical condition: Neovascular Age Related Macular Degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) SK (Completed) LV (Completed) AT (Completed) ES (Ongoing) BG (Completed) EE (Completed) LT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000422-36 | Sponsor Protocol Number: SB11-G31-AMD | Start Date*: 2017-11-28 | |||||||||||
Sponsor Name:Samsung Bioepis Co., Ltd. | |||||||||||||
Full Title: A Phase III Randomised, Double-masked, Parallel Group, Multicentre Study to Compare the Efficacy, Safety, Pharmacokinetics and Immunogenicity between SB11 (proposed ranibizumab biosimilar) and Luce... | |||||||||||||
Medical condition: Neovascular Age-related Macular Degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) HU (Completed) GB (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: 2018-004486-13 | Sponsor Protocol Number: QL1205-002 | Start Date*: 2019-04-18 | |||||||||||
Sponsor Name:Qilu Pharmaceutical Co., Ltd. | |||||||||||||
Full Title: A Randomized, Phase 3, Double-masked, Parallel-group, Multicenter Study to Compare Efficacy and Safety of QL1205 Versus Lucentis® in Subjects With Neovascular Age-related Macular Degeneration | |||||||||||||
Medical condition: Subjects With Wet (neovascular) Age-related Macular Degeneration (wAMD), aged ≥50 years | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) SK (Completed) CZ (Completed) LV (Completed) PL (Completed) BG (Completed) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002930-19 | Sponsor Protocol Number: XBR1001 | Start Date*: 2019-02-25 | |||||||||||
Sponsor Name:Xbrane Biopharma | |||||||||||||
Full Title: A Phase III Double-Blind, Parallel Group, Multicenter Study to Compare the Efficacy and Safety of Xlucane versus Lucentis® in Patients with Neovascular Age-Related Macular Degeneration | |||||||||||||
Medical condition: Wet Age-related macular degeneration (AMD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Completed) LT (Completed) HU (Completed) SK (Completed) LV (Completed) CZ (Completed) BG (Completed) PL (Completed) ES (Ongoing) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019079-32 | Sponsor Protocol Number: 190342-033D | Start Date*: 2010-05-19 |
Sponsor Name:Allergan Limited | ||
Full Title: A Multicenter, Patient-Masked, Safety Extension Study to Evaluate the Biodegradation of the Brimonidine Tartrate Posterior Segment Drug Delivery System | ||
Medical condition: Patients who participated in a previous intravitreal Brimo PS DDS study, including 190342-028D (Retinitis pigmentosa) and 190342-032D (Geographic Atrophy from Age-related Macular Degeneration). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PT (Completed) DE (Completed) GB (Completed) CZ (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001063-82 | Sponsor Protocol Number: KS301P105 | Start Date*: 2021-01-14 | ||||||||||||||||||||||||||
Sponsor Name:Kodiak Sciences Inc. | ||||||||||||||||||||||||||||
Full Title: A Prospective, Randomized, Double-masked, Active Comparator-controlled, Multi-center, Two-arm, Phase 3 Study to Evaluate the Efficacy and Safety of Intravitreal KSI-301 Compared with Intravitreal A... | ||||||||||||||||||||||||||||
Medical condition: Diabetic Macular Edema (DME) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: CZ (Prematurely Ended) HU (Prematurely Ended) FR (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-004601-14 | Sponsor Protocol Number: PAN-01-102 | Start Date*: 2018-06-25 | |||||||||||
Sponsor Name:PanOptica, Inc. | |||||||||||||
Full Title: A Randomized, Double Masked, Uncontrolled, Multicenter Phase I/II Study to Evaluate Safety and Tolerability of PAN-90806 Eye Drops, Suspension in Treatment-Naïve Participants with Neovascular Age-R... | |||||||||||||
Medical condition: Neovascular Age-Related Macular Degeneration (AMD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) LV (Completed) CZ (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
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