- Trials with a EudraCT protocol (19)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (29)
19 result(s) found for: Keratoconjunctivitis.
Displaying page 1 of 1.
EudraCT Number: 2007-002455-16 | Sponsor Protocol Number: LTGV550-PII-11/06 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Laboratoires Théa | |||||||||||||
Full Title: Efficacy and safety of GV 550 in acute adenoviral keratoconjunctivitis | |||||||||||||
Medical condition: acute adenoviral keratoconjunctivitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005882-37 | Sponsor Protocol Number: 524 | Start Date*: 2008-01-17 | |||||||||||
Sponsor Name:BAUSCH&LOMB | |||||||||||||
Full Title: RANDOMIZED CONTROLLED CLINICAL STUDY ON THE EFFICACY AND TOLERABILITY OF 0.4% HYALURONIC ACID HYPOTONIC EYE DROPS (IALUREX) VS. HYDROXYPROPYL-GUAR EYE DROPS (SYSTANE) IN THE TREATMENT OF DRY EYE SY... | |||||||||||||
Medical condition: Dry eye syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002101-50 | Sponsor Protocol Number: ACU01-100 | Start Date*: 2007-06-11 | |||||||||||||||||||||
Sponsor Name:Acuity Pharmaceuticals, LLC | |||||||||||||||||||||||
Full Title: A Phase 2, randomized, double-masked, placebo-controlled, parallel-assignment study of topical N-Chlorotaurine (NCT) formulated with ammonium chloride administered for 10 days in patients with epid... | |||||||||||||||||||||||
Medical condition: Epidemic adenoviral keratoconjunctivitis (EKC) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: AT (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003391-35 | Sponsor Protocol Number: LT1910-PIV-01/06 (NL) | Start Date*: 2006-09-13 | |||||||||||
Sponsor Name:Laboratoires THEA | |||||||||||||
Full Title: Evaluation of the efficacy and safety of unpreserved dexamethasone phosphate 0.1% eye drops (T1910) versus placebo in patients with bilateral treated severe keratoconjunctivitis sicca due to Sjögre... | |||||||||||||
Medical condition: keratoconjunctivitis sicca | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004614-25 | Sponsor Protocol Number: 20171117 | Start Date*: 2018-02-09 | |||||||||||
Sponsor Name:Helsinki Eye Hospital | |||||||||||||
Full Title: Adenoviruksen aiheuttaman silmätulehduksen hoito | |||||||||||||
Medical condition: silmän adenoinfektion hoito | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005694-31 | Sponsor Protocol Number: 2012/ADE002 | Start Date*: 2013-07-05 | |||||||||||
Sponsor Name:Adenovir Pharma AB | |||||||||||||
Full Title: Evaluation of the Therapeutic Efficacy of APD-209 Eye Drops in Treatment of Acute Phase Adenoviral-Induced Epidemic Keratoconjunctivitis (EKC). A Randomised, Double-Masked, Placebo-Controlled, Mult... | |||||||||||||
Medical condition: Acute phase Adenoviral-induced Epidemic Keratoconjunctivitis, EKC | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012446-23 | Sponsor Protocol Number: 192371-016 | Start Date*: 2009-10-30 | |||||||||||
Sponsor Name:Allergan Ltd | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Masked, Parallel-Group Study Evaluating the Efficacy and Safety of Cyclosporine Ophthalmic Solution 0.010% Compared with its Vehicle Administered QID for 3 months ... | |||||||||||||
Medical condition: Atopic Keratoconjunctivitis is a bilateral, inflammatory external ocular disease. A serious disease driven by chronic inflammation of the cornea, conjunctiva and lower lid. AKC is commonly presen... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) ES (Completed) FR (Completed) CZ (Completed) IT (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000029-23 | Sponsor Protocol Number: NVG06C103 | Start Date*: 2008-10-16 | |||||||||||
Sponsor Name:Novagali Pharma S.A. | |||||||||||||
Full Title: A Phase III, Multicenter, Randomized, Controlled, Double-Masked Trial of NOVA22007 (Ciclosporin 0.1%) Ophthalmic Cationic Emulsion versus Vehicle in Patients with Moderate to Severe Dry Eye Syndrome | |||||||||||||
Medical condition: Keratoconjunctivitis sicca (KCS), or dry eye syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) FR (Completed) ES (Completed) IT (Completed) DE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002835-40 | Sponsor Protocol Number: AK701 | Start Date*: 2020-01-28 | ||||||||||||||||||||||||||
Sponsor Name:Akari Therapeutics Plc | ||||||||||||||||||||||||||||
Full Title: Topical rVA576 for treatment of atopic keratoconjunctivitis: a randomised placebo double masked parallel trial (TRACKER) | ||||||||||||||||||||||||||||
Medical condition: Moderate to severe atopic keratoconjunctivitis (AKC), Vernal keratoconjunctivitis (VKC), Severe allergic conjunctivitis (seasonal (SAC) or perennial (PAC)) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-002804-38 | Sponsor Protocol Number: AMASS | Start Date*: 2020-08-12 | |||||||||||
Sponsor Name:Rigshospitalet-Glostrup | |||||||||||||
Full Title: A randomized clinical trial evaluating allogeneic adipose-derived mesenchymal stem cells as a treatment of dry eye disease in Sjögren's Syndrome | |||||||||||||
Medical condition: The trial will include participants with Aqueous Deficient Dry Eye Disease due to Sjögrens syndrom (International Classification of Diseases-10: DM 350A) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000160-97 | Sponsor Protocol Number: NVG10E117 | Start Date*: 2011-04-08 | ||||||||||||||||||||||||||
Sponsor Name:NOVAGALI Pharma S.A. | ||||||||||||||||||||||||||||
Full Title: A MULTICENTER, RANDOMIZED, DOUBLE-MASKED, 2 PARALLEL ARM, VEHICLE CONTROLLED, 6-MONTH PHASE III TRIAL WITH A 6 MONTH OPEN LABEL TREATMENT SAFETY FOLLOW-UP PERIOD TO EVALUATE THE EFFICACY AND SAFETY... | ||||||||||||||||||||||||||||
Medical condition: Severe Dry Eye Disease | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: SE (Completed) BE (Completed) DE (Completed) IT (Ongoing) AT (Completed) GB (Completed) CZ (Completed) ES (Ongoing) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-000991-34 | Sponsor Protocol Number: DMP 81.1.05 | Start Date*: 2006-04-21 |
Sponsor Name:Dr. Gerhard Mann, Chem-pharm. Fabrik GmbH | ||
Full Title: A randomized, double-blind, monocentric phase IV clinical study on the ocular tolerability of a topical ophthalmic product containing Retinolpalmitat 1000 I.U. in comparison to a reference product ... | ||
Medical condition: Patients suffering from keratoconjunctivitis sicca (dry eye) and break-up-time (BUT) values < 10 sec | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-002066-12 | Sponsor Protocol Number: NVG12D122 | Start Date*: 2012-12-13 | ||||||||||||||||||||||||||
Sponsor Name:NOVAGALI Pharma S.A.S | ||||||||||||||||||||||||||||
Full Title: A Multicenter, Open Label, Interventional, Prospective, Non Randomized, One Cohort Extension Study To Assess the Sustainability of the Effect of NOVA22007 Following Treatment Discontinuation in Imp... | ||||||||||||||||||||||||||||
Medical condition: Severe Dry Eye Disease | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: CZ (Completed) BE (Completed) AT (Completed) DE (Completed) GB (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005060-10 | Sponsor Protocol Number: NVG09B113 | Start Date*: 2013-04-08 | |||||||||||
Sponsor Name:Novagali Pharma S.A.S. | |||||||||||||
Full Title: A MULTICENTER, RANDOMIZED, DOUBLE-MASKED, 3 PARALLEL ARMS, PLACEBO CONTROLLED STUDY TO ASSESS THE EFFICACY AND SAFETY OF NOVA22007 1MG/ML (CICLOSPORIN/CYCLOSPORINE) EYE DROPS, EMULSION ADMINISTERED... | |||||||||||||
Medical condition: Vernal Keratoconjunctivitis (VKC) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) IT (Completed) DE (Completed) PT (Completed) ES (Completed) GR (Completed) HR (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003689-32 | Sponsor Protocol Number: FARM5YZTZW | Start Date*: 2006-12-19 | |||||||||||
Sponsor Name:UNIVERSITA CAMPUS BIOMEDICO | |||||||||||||
Full Title: Multicenter, randomised, double masked, controlled studies on the efficacy of Cyclosporine eye drop treatment in preventing Vernal Keratoconjunctivitis VKC relapses and in treating the acute phase. | |||||||||||||
Medical condition: VERNAL KERATOCONJUNTIVITIS | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001502-17 | Sponsor Protocol Number: FARM6FYZB3 | Start Date*: 2007-11-15 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA MEYER | |||||||||||||
Full Title: MULTICENTRIC COMPARATIVE RANDOMIZED DOUBLE BLIND CROSS OVER STUDY WITH TACROLIMUS (FK506)0.1% EYEDROPS AND CYCLOSPORINE 1% EYEDROPS IN CHILDREN WITH SEVERE ACTIVE VERNAL KERATOCONJUNCTIVITIS, LASTI... | |||||||||||||
Medical condition: Vernal Keratoconjunctivitis | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004929-33 | Sponsor Protocol Number: SiccaIkervis | Start Date*: 2018-12-05 |
Sponsor Name:KH Hietzing, Department of Ophthalmology | ||
Full Title: Effect of Ciclosporin eyedrops on ocular symptoms and optical image quality in patients with primary or secondary Sjögren syndrome | ||
Medical condition: primary or secondary Sjögren Syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-007984-17 | Sponsor Protocol Number: PETC1002 | Start Date*: 2009-03-02 | |||||||||||
Sponsor Name:Moorfields Eye Hospital NHS Foundation Trust | |||||||||||||
Full Title: Pilot randomised placebo-controlled double-masked clinical trial of subconjunctival Bevacizumab on eyes with recent onset of corneal neovascularisation | |||||||||||||
Medical condition: Corneal neovascularisation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024254-11 | Sponsor Protocol Number: CF101-301KCS | Start Date*: 2011-03-30 | |||||||||||
Sponsor Name:Can-Fite BioPharma, Ltd | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Masked, Placebo-Controlled, Dose-Finding, Parallel-Group Study of the Safety and Efficacy of Daily CF101 Administered Orally in Patients with Moderate-to-Severe Dry Ey... | |||||||||||||
Medical condition: Moderate-to-severe Dry Eye disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
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