Myopia
Conditions
Brief summary
The objective of this clinical investigation is to evaluate the efficacy and safety of SAT-001 designed as Software as Medical Device (SaMD) for slowing myopia progression and treatment in pediatric myopia patients.
Detailed description
Myopia is a common refractive error affecting approximately 30 % of the global population, with even higher prevalence in Asian countries including Korea. This study is a confirmatory clinical trial designed to evaluate the efficacy and safety of SAT-001 for slowing the progression of myopia in children, based on the results of the exploratory clinical trial.
Interventions
DEVICESAT-001
Device: SAT-001(a Software as Medical Device) Using SAT-001 application for 48 weeks and wearing single vision spectacles
Wearing single vision spectacles
Sponsors
S-Alpha Therapeutics, Inc.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
5 Years to 8 Years
Healthy volunteers
No
Inclusion criteria
1. Children aged 5 to less than 9 2. Meet the following refractive criteria by cycloplegic refraction 1. Spherical equivalent refractive error (SER): -0.75 to less than -6.00 D in each eye 2. Astigmatism of 1.50 D or less in each eye 3. Anisometropia of 2.00 D or less 3. Best corrected visual acuity of 0.2 logMAR or better in each eye at the Screening Visit 4. Able to successfully accomplish SAT-001, the investigational device (able to follow the written and verbal instruction) 5. Subjects and their legal guardians who agree to participate in the clinical trial and are willing to provide the signed informed consent after receiving and comprehending the explanation of the description of this clinical trial (subject under 6 can make a mark for agreement after full information and understanding)
Exclusion criteria
1. History of atropine use within 3 days prior to Baseline (Visit 2) (prior treatment of myopia control with low dose atropine within 1 month prior to Baseline) 2. Current or prior use of multifocal lenses (e.g. progressive addition lenses), orthokeratology (Ortho-K, e.g. Dream lens), or Rigid gas permeable (RGP) within 1month prior to Baseline(Visit 2) 3. Ocular abnormalities in cornea, lens, central retina, iris, ciliary body, etc., or presence of malignant tumors in the orbital area 4. History of eye diseases such as manifest strabismus, intermittent strabismus, amblyopia, and nystagmus (excluding strabismus that maintains binocular vision) 5. History of ocular surgery such as eyelid surgery, strabismus surgery, intraocular surgery, or refractive correction surgery (excluding simple double eyelid surgery) 6. Down's syndrome or cerebral palsy 7. Within 6 months prior to the Screening visit (Visit 1), has experience of other clinical trial medications or investigational device 8. Clinically significant systemic diseases such as congenital heart disease, respiratory disease, endocrine disease, and neurological disease that the investigator may consider inappropriate for participation in the clinical trials 9. Systemic diseases that could impact both vision and visual field 10. History of growth hormone treatment within 1 month prior to Baseline (Visit 2) 11. Other reasons for participation in the trial at the discretion of the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in Axial Length | Baseline, 48weeks |
Secondary
| Measure | Time frame |
|---|---|
| Change in Axial Length | Baseline, 12weeks, 24weeks, 36weeks |
| Change in cycloplegic Spherical Equivalent Refractive Error | Baseline, 24weeks, 48weeks |
| Change in cycloplegic Spherical Equivalent Refractive Error relative to baseline depending on the myopia severity(mild myopia, moderate myopia) | Baseline, 24 weeks, 48 weeks |
| Change in axial length relative to baseline depending on the myopia severity(mild myopia, moderate myopia) | Baseline, 12weeks, 24weeks, 36weeks, 48weeks |
Countries
South Korea
Contacts
Primary ContactYS Park
Outcome results
None listed