- Trials with a EudraCT protocol (565)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
565 result(s) found for: Eye Diseases AND Eye Disease.
Displaying page 3 of 29.
EudraCT Number: 2020-001061-37 | Sponsor Protocol Number: KS301P103 | Start Date*: 2020-12-11 | |||||||||||||||||||||||||||||||
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: Macular edema secondary to retinal vein occlusion | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: LV (Prematurely Ended) DE (Completed) SK (Prematurely Ended) CZ (Prematurely Ended) FR (Prematurely Ended) HU (Completed) IT (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-006794-37 | Sponsor Protocol Number: VRDN-001-101 | Start Date*: 2022-05-20 | |||||||||||
Sponsor Name:Viridian Therapeutics, Inc. | |||||||||||||
Full Title: A multiple ascending dose (MAD) safety, tolerability and efficacy study of VRDN-001, a humanized monoclonal antibody directed against the IGF-1 receptor, in normal healthy volunteers (NHVs) and sub... | |||||||||||||
Medical condition: Thyroid eye disease (TED) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) DE (Trial now transitioned) NL (Trial now transitioned) IT (Completed) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003428-35 | Sponsor Protocol Number: KSI-CL-102 | Start Date*: 2020-01-03 | |||||||||||||||||||||
Sponsor Name:Kodiak Sciences Inc. | |||||||||||||||||||||||
Full Title: A Phase 2b/3, Prospective, Randomised, Double-masked, Active Comparator-controlled, Multi-center Study to Investigate the Efficacy and Safety of Repeated Intravitreal Administration of KSI-301 in S... | |||||||||||||||||||||||
Medical condition: Neovascular (Wet) Age-related Macular Degeneration | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: LV (Prematurely Ended) GB (GB - no longer in EU/EEA) DE (Prematurely Ended) CZ (Prematurely Ended) SK (Prematurely Ended) PL (Prematurely Ended) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-002780-13 | Sponsor Protocol Number: C-07-63 | Start Date*: 2008-09-04 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Alcon Research, Ltd. | ||||||||||||||||||||||||||||||||||||||
Full Title: A Three-Month, Multicenter, Double-Masked Study Comparing the Safety and Efficacy of the Fixed Combination Travoprost + Brinzolamide Eye Drops, Suspension vs Travatan vs Azopt in Patients with Open... | ||||||||||||||||||||||||||||||||||||||
Medical condition: open-angle glaucoma or ocular hypertension | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) DE (Prematurely Ended) ES (Completed) BE (Completed) HU (Prematurely Ended) GB (Prematurely Ended) IT (Prematurely Ended) PT (Prematurely Ended) AT (Prematurely Ended) LV (Completed) SE (Prematurely Ended) EE (Prematurely Ended) LT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-002787-68 | Sponsor Protocol Number: IMVT-1401-3201 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Immunovant Sciences, GmbH | |||||||||||||
Full Title: A Phase 3, Multi-center, Randomized, Quadruple-masked, Placebo-controlled Study of Batoclimab for the Treatment of Participants with Active Thyroid Eye Disease (TED) | |||||||||||||
Medical condition: Thyroid Eye Disease (TED) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) IT (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003285-27 | Sponsor Protocol Number: T1565-PIV-0117 | Start Date*: 2017-09-26 | |||||||||||
Sponsor Name:Laboratoires Thea | |||||||||||||
Full Title: Clinical efficacy of topical hydrocortisone 0.335% (Softacort®) in patients with chronic dry eye disease and associated ocular surface inflammation | |||||||||||||
Medical condition: Dry Eye Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002698-20 | Sponsor Protocol Number: OPT-302-1002 | Start Date*: 2018-02-07 | |||||||||||||||||||||
Sponsor Name:Opthea Ltd | |||||||||||||||||||||||
Full Title: A dose-ranging study of intravitreal OPT-302 in combination with ranibizumab, compared with ranibizumab alone, in participants with neovascular age-related macular degeneration (wet AMD) | |||||||||||||||||||||||
Medical condition: Neovascular age-related macular degeneration (wet AMD) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) LV (Completed) GB (Completed) ES (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-002547-27 | Sponsor Protocol Number: OP/CD001 | Start Date*: 2005-09-03 |
Sponsor Name:University of Bristol | ||
Full Title: Combined Immunosuppression and Radiotherapy in Thyroid Eye Disease | ||
Medical condition: Thyroid Eye Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-002788-30 | Sponsor Protocol Number: IMVT-1401-3202 | Start Date*: 2023-07-13 | |||||||||||
Sponsor Name:Immunovant Sciences, GmbH | |||||||||||||
Full Title: A Phase 3, Multi-center, Randomized, Quadruple-masked, Placebo-controlled Study of Batoclimab for the Treatment of Participants with Active Thyroid Eye Disease (TED) | |||||||||||||
Medical condition: Thyroid Eye Disease (TED) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) BE (Trial now transitioned) LV (Trial now transitioned) HU (Trial now transitioned) SK (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-002931-32 | Sponsor Protocol Number: APL2-GA-305 | Start Date*: 2021-09-17 | |||||||||||
Sponsor Name:Apellis Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase 3 open-label, multicenter, extension study to evaluate the long-term safety and efficacy of pegcetacoplan in subjects with geographic atrophy secondary to age-related macular degeneration | |||||||||||||
Medical condition: Geographic Atrophy Secondary to Age-Related Macular Degeneration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) DE (Trial now transitioned) FR (Trial now transitioned) CZ (Trial now transitioned) PL (Trial now transitioned) ES (Ongoing) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001064-29 | Sponsor Protocol Number: KS301P106 | Start Date*: 2021-09-26 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Kodiak Sciences Inc. | ||||||||||||||||||||||||||||||||||||||
Full Title: A Prospective, Randomized, Double-masked, Sham-controlled, Multi-center, Two-arm, Phase 3 Study to Evaluate the Efficacy and Safety of Intravitreal KSI-301 in Participants with Moderately Severe to... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Non-proliferative Diabetic Retinopathy (NPDR) | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: SK (Prematurely Ended) ES (Prematurely Ended) LV (Prematurely Ended) CZ (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-001062-11 | Sponsor Protocol Number: KS301P104 | Start Date*: 2021-01-20 | ||||||||||||||||||||||||||
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: DE (Prematurely Ended) LV (Prematurely Ended) SK (Prematurely Ended) HU (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-002781-66 | Sponsor Protocol Number: C-08-16 | Start Date*: 2008-12-04 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Alcon Research, Ltd. | ||||||||||||||||||||||||||||||||||||||
Full Title: A twelve-month, multicenter, double-masked study of Travoprost / Brinzolamide fixed combination QD AM and Travoprost / Brinzolamide fixed combination QD PM versus COSOPT BID in patients with open-a... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Open-angle glaucoma or Ocular hypertension | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) FR (Completed) ES (Completed) BE (Completed) SE (Prematurely Ended) DK (Prematurely Ended) PL (Completed) IT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-001662-35 | Sponsor Protocol Number: BTIIMD-02-EC/22/GLAUCOMA | Start Date*: 2022-08-18 |
Sponsor Name:BTI I MAS D S.L. | ||
Full Title: Randomized, double-blind, parallel group clinical trial to evaluate the efficacy and safety of PRGF eye drops as a treatment for dry eye disease in patients with glaucoma | ||
Medical condition: Dry eye disease in patients with glaucoma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001720-33 | Sponsor Protocol Number: CSA_2020 | Start Date*: 2020-09-08 | |||||||||||
Sponsor Name:UNIVERSITĂ€ CAMPUS BIO-MEDICO DI ROMA | |||||||||||||
Full Title: Cyclosporine 0.1% Eye Drops as Prophylactic Treatment in Post Surgical Ocular Surface System Failure Within The Age | |||||||||||||
Medical condition: High-risk patients, i.e. elder patients, who show dry eye syndrome after insult. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020855-29 | Sponsor Protocol Number: E1496/09 | Start Date*: 2009-10-16 | ||||||||||||||||
Sponsor Name:UNIVERSITA' DEGLI STUDI DI MESSINA | ||||||||||||||||||
Full Title: Radioiodine ablation of post-surgical thyroid remnants by recombinant human TSH (rhTSH) in patients with moderately severe and severe Graves' orbithopathy (GO) | ||||||||||||||||||
Medical condition: Patients affected with moderately severe and severe GO | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002750-38 | Sponsor Protocol Number: C-08-09 | Start Date*: 2008-10-22 | |||||||||||||||||||||
Sponsor Name:Alcon Research Ltd | |||||||||||||||||||||||
Full Title: 24-hour IOP control with Travoprost / Brinzolamide fixed combination once-daily (QD)in the evening vs TRAVATAN | |||||||||||||||||||||||
Medical condition: Open-angle glaucoma or ocular hypertension | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-000429-17 | Sponsor Protocol Number: 00 | Start Date*: 2021-05-20 |
Sponsor Name:University of Oslo, Faculty of Medicine, Institute of Health and Society | ||
Full Title: BASIC - Better treatment for acute sinusitis in primary care: a randomized controlled trial testing topical treatment with chloramphenicol eye drops | ||
Medical condition: Acute rhinosinusitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001172-36 | Sponsor Protocol Number: DX211 | Start Date*: 2017-08-09 | |||||||||||
Sponsor Name:Oculis ehf. | |||||||||||||
Full Title: Efficacy and safety of dexamethasone nanoparticles eye drops in diabetic macular edema. | |||||||||||||
Medical condition: Diabaetic macular edema | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) FI (Completed) HU (Completed) LV (Completed) EE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-001178-70 | Sponsor Protocol Number: BECRO/ACT/ORASIS-LT | Start Date*: 2023-01-26 | |||||||||||||||||||||
Sponsor Name:actrevo GmbH | |||||||||||||||||||||||
Full Title: Non-inferiority, Randomized, Observer-blind, two Parallel Group, Clinical Trial for Comparing the Efficacy and Tolerability of a new Generic BAC-free Formulation of Latanoprost/Timolol 0.05 mg/mL +... | |||||||||||||||||||||||
Medical condition: Open angle glaucoma or ocular hypertension | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GR (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
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