0.1% Tβ4 Ophthalmic Solution for Dry Eye Symptoms and Signs
Thymosin beta 4
+ Placebo
Maladies oculaires
+ Maladies de l'appareil lacrymal
+ Syndromes de l'œil sec
Étude thérapeutique
Résumé
Date de début de l'étude : 1 août 2011
Date à laquelle le premier participant a commencé l'étude.This study is about evaluating the safety and effectiveness of a treatment called Tβ4 Ophthalmic Solution for dry eye syndrome. Dry eye syndrome is a condition where the eyes do not produce enough tears or the tears evaporate too quickly, leading to discomfort and vision problems. Tβ4 is a substance that promotes wound repair and regeneration in various tissues, including the eye. It has shown promising results in repairing corneal wounds and reducing corneal staining in nonclinical studies and compassionate-use cases. This study aims to further explore its potential in treating dry eye syndrome, targeting individuals suffering from this condition. The study's outcomes could potentially lead to a new safe and effective therapeutic option for dry eye syndrome. During the study, participants will receive either the Tβ4 Ophthalmic Solution or a placebo (a solution with no active ingredients). The treatment will be administered as eye drops. The study will take place in a controlled adverse environment, a regulated setting designed to exacerbate dry eye signs and symptoms. Two primary outcomes will be measured: corneal staining in the worst eye and ocular discomfort in the worst eye. Corneal staining will be tested using a special dye and light, while ocular discomfort will be measured using a validated 4-point scale. Both tests will be conducted throughout the study until the end of treatment on Day 29. The 'worst eye' is determined as the eye with the greater increase of inferior corneal staining or ocular discomfort. If both eyes are equal, the right eye is chosen as the worst eye.
Protocole
Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.72 participants à inclure
Nombre total de participants que l'essai clinique vise à recruter.Traitement
Éligibilité
Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.Tout sexe
Le sexe biologique des participants éligibles à s'inscrire.De 18 à 85 ans
Tranche d'âge des participants éligibles à participer.Volontaires sains non autorisés
Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.Conditions
Pathologie
Critères
Inclusion Criteria: 1. Have given a written, informed consent. 2. Be able and willing to follow instructions, including participation in study assessments, and be present for the required study visits for the duration of the study. 3. Have a best corrected visual acuity. 4. Have a patient-reported history of dry eye in both eyes. 5. Use and/or desire to use an artificial tear substitute for dry eye symptoms within the past 6 months. 6. A negative urine pregnancy test if female of childbearing potential. 7. Have a corneal fluorescein staining score of ≥ 2 in any corneal surface segment in at least one eye at Visit 1. \- Exclusion Criteria: 1. Have contraindications to the use of the study drug. 2. Have known allergy or sensitivity to the study drug or components thereof. 3. Have anterior blepharitis. 4. Be diagnosed with an on-going ocular infection or active ocular inflammation. 5. Use contact lenses within 1 week before Visit 1 or during the course of the study. 6. Have previously had Laser-Assisted in Situ Keratomileusis (LASIK) surgery within 12 months prior to Visit 1. 7. Be currently taking any topical ophthalmic prescription or over-the-counter (OTC) solutions, artificial tears, gels, or scrubs and cannot discontinue these medications for the duration of the trial. 8. Have used topical ocular cyclosporine within 30 days prior to Visit 1. 9. Have had a past or present evidence of malignancy.
Plan de l'étude
Découvrez tous les traitements administrés dans cette étude, leur description détaillée et ce qu'ils impliquent.2 groupes d'intervention sont désignés dans cette étude
50% de chances d'être dans le groupe placebo en aveugle
Groupes de traitement
Groupe I
Comparateur actifGroupe II
PlaceboObjectifs de l'étude
Objectifs principaux
Objectifs secondaires