Study to Evaluate the Efficacy of Alleance® (Atropine Sulfate 0.01%) as a Treatment to Delay Myopia and Axial Ocular Elongation in Children.

Laboratorios Sophia

Status and phase

Enrolling

Phase 3

Conditions

Myopia

Myopia, Progressive

Treatments

Drug: Alleance®

Drug: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT06389110

SOPH201-1023/III

Details and patient eligibility

About

Phase III clinical study to evaluate the efficacy of Alleance® (atropine sulfate 0.01%) ophthalmic solution through the incidence of unexpected adverse events, changes in Best Corrected Visual Acuity (BCVA), changes in intraocular pressure, changes in the amplitude of accommodation, compared to placebo, as a treatment to delay the progression of myopia and axial ocular elongation in children.

Full description

This is a study to demonstrate superiority, double-blind, randomized, controlled, comparative, and multicenter phase III clinical trial.

Primary Objective:

To demonstrate the superiority of Alleance® compared to placebo in delaying myopia progression in children.

Specific objectives:

To demonstrate the reduction in progression in spherical equivalent in children using Alleance® compared to placebo after 12 months of treatment.
To demonstrate the reduction in progression in ocular axial length in children using Alleance® compared to placebo, after 12 months of treatment.

Secondary objectives:

To compare the incidence of adverse events related to the interventions.
Compare the incidence of photophobia between interventions.
To assess pupillary diameter between the interventions.
To assess best-corrected far visual acuity between interventions.
To assess near best-corrected visual acuity between interventions.
To assess the amplitude of accommodation between interventions.
Assess intraocular pressure (IOP) between procedures.

Enrollment

123 estimated patients

Sex

All

Ages

3 to 12 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Children aged between 3 to 12 years
Male or female sex.
The parent(s) or legal guardian(s) must voluntarily give their signed informed consent.
From the age of 7 years and older, the subject's willingness to participate in the research study will be expressed in writing. In the case of subjects under 7 years of age, only the signature of the informed consent by the parent(s) or legal guardian(s) will be required, provided that the subject's verbally expressed will is respected.
Ability and willingness to comply with the scheduled visits, treatment plan and other study procedures.
Female subjects, who have already presented their menarche, must have a negative urine pregnancy test at the time of screening.
Female subjects who have already experienced menarche should secure a method of contraception for the duration of the study. Acceptable contraceptive methods include abstinence (defined as abstinence from heterosexual intercourse from study entry until completion) or use of a highly effective contraceptive method, including hormonal contraception, barrier methods or intrauterine device).
Refractive error of spherical equivalent between -0.50 to -6.00 D in each eye, measured by autorefraction and cycloplegic retinoscopy.
Astigmatism less than -1.50 D in each eye, measured by autorefraction and retinoscopy.
Spherical equivalent anisometropia ≤ 1.50 D measured by autorefraction and cycloplegic retinoscopy.
Best corrected visual acuity (BCVA) normal for age.
Normal binocular function and stereopsis for age.
Normal intraocular pressure (< 21 mmHg).
Gestational age ≥ 32 weeks and birth weight > 1500 g.

Exclusion criteria

Allergy to atropine or any of the components of the investigational products.
Previous or current use of atropine, orthokeratology lens or other optical methods for myopia control (bifocal, progressive, multifocal, or defocusing air or contact lenses). Only prior or current use of frame lenses or monofocal contact lenses for the correction of myopic or myopic/astigmatic refractive error will be allowed.

History or current history of amblyopia or manifest strabismus, including intermittent tropia.

Heart rate > 120 beats per minute persistently (for more than 10 minutes) at the time of screening/baseline visit.
History of any disease or syndrome predisposing the subject to severe myopia (Marfan syndrome, Stickler syndrome, retinopathy of prematurity, etc.).
History of serious systemic disease that, in the investigator's judgment, would make the subject ineligible (e.g., cardiac, endocrine, respiratory, neurologic [infantile cerebral palsy], Down syndrome, etc.).
History or current history of glaucoma or ocular hypertension.
History of any refractive ocular anatomical anomaly (keratoconus, lenticonus, spherophakia, aphakia, etc.).
History of ocular diseases, excluding myopia (corneal alterations/opacities, cataract, retinal alterations, inflammatory diseases, etc.).
History of any type of ocular surgery.
For female subjects who have presented their menarche: being pregnant or breastfeeding.
Having participated in clinical research studies 30 days prior to inclusion in the present study.
Previous participation in this study.
Present unresolved ocular lesions or trauma at the time of study entry.
Present active inflammatory or infectious ocular disease at the time of study entry.
Having undergone surgical procedures, not ophthalmologic, within the last 3 months.
Chronic use of any topical or systemic antimuscarinic/anticholinergic medication (atropine, scopolamine, tropicamide) within 21 days prior to screening, and/or anticipated need for its chronic use during the study period (more than 7 consecutive days in a month or more than 30 days total in a year). The use of cycloplegic drops for ophthalmologic examination is allowed.
Be or have an immediate family member (e.g., parent/legal guardian or sibling) who is part of the research site or sponsor´s staff.

Elimination Criteria:

Withdrawal of their consent to participate in the study (informed consent form).
Occurrence of a serious adverse event, whether related or not to the interventions, that in the opinion of the principal investigator (PI) and/or the sponsor, could affect the patient's fitness to safely continue with the study procedures.
Non-tolerability or hypersensitivity to any of the compounds used during the tests -(fluorescein, tetracaine).
Non-tolerability or hypersensitivity to any of the drugs under investigation.
Adherence < 80% determined by the subject's diary and corroborated by the final weight of the research products (RP) compared to the initial weight.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

123 participants in 2 patient groups, including a placebo group

Alleance®

Active Comparator group

Description:

Alleance®. Atropine sulfate 0.01%. Ophthalmic solution. * Dosage: 1 drop QD \[1\] (once a day), at night, for 12 months. * Route of administration: Ophthalmic

Treatment:

Drug: Alleance®

Placebo

Placebo Comparator group

Description:

* Placebo. Ophthalmic solution. * Dosage: 1 drop QD \[1\] (once a day), at night, for 12 months. * Route of administration: Ophthalmic

Treatment:

Drug: Placebo