Pivotal Study of SAT-001 in Treatment of Pediatric Patient With Myopia

Recruiting now · Not applicable

Conditions studied: Myopia

In brief

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.

Key facts

Study ID

NCT06344572

Run by

S-Alpha Therapeutics, Inc.

People needed

110

Starts

2023-09-27

Expected to finish

2025-09-30

Last updated by the study team

2025-08-13

Who can join

Age: 5 and older, up to 8. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Children aged 5 to less than 9
• Meet the following refractive criteria by cycloplegic refraction
• Spherical equivalent refractive error (SER): -0.75 to less than -6.00 D in each eye
• Astigmatism of 1.50 D or less in each eye
• Anisometropia of 2.00 D or less
• Best corrected visual acuity of 0.2 logMAR or better in each eye at the Screening Visit
• Able to successfully accomplish SAT-001, the investigational device (able to follow the written and verbal instruction)
• 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)

You may not qualify if…

• 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)
• 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)
• Ocular abnormalities in cornea, lens, central retina, iris, ciliary body, etc., or presence of malignant tumors in the orbital area
• History of eye diseases such as manifest strabismus, intermittent strabismus, amblyopia, and nystagmus (excluding strabismus that maintains binocular vision)
• History of ocular surgery such as eyelid surgery, strabismus surgery, intraocular surgery, or refractive correction surgery (excluding simple double eyelid surgery)
• Down's syndrome or cerebral palsy
• Within 6 months prior to the Screening visit (Visit 1), has experience of other clinical trial medications or investigational device
• 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
• Systemic diseases that could impact both vision and visual field
• History of growth hormone treatment within 1 month prior to Baseline (Visit 2)
• Other reasons for participation in the trial at the discretion of the investigator

Where it is running

• Gachon University Gil Hospital — Incheon, South Korea (enrolling)

Full record on ClinicalTrials.gov

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