Exploratory Study on the Effect of SAT-001 on Choroidal Thickness in Pediatric Myopia Patients

Not Applicable

Completed

• Conditions: Myopia

• Registration Number: NCT06729723
• Lead Sponsor: S-Alpha Therapeutics, Inc.

Brief Summary

This clinical trial aims to exploratively compare and evaluate the structural changes in the eye (specifically changes in choroidal thickness) pre- and post-treatment of the investigational medical devices ('SAT-001' and 'modified SAT-001') in pediatric myopia patients, and the differences in their effects on the eye.

Detailed Description

Myopia is a rapidly growing global concern, particularly in pediatric populations, with high rates of progression and the potential for serious long-term consequences. The risk of developing high myopia, which can lead to complications such as retinal detachment, cataracts, glaucoma, and optic nerve abnormalities, underscores the importance of effective management strategies for pediatric myopia. While treatments to slow myopia progression have been explored, including pharmacological and non-pharmacological approaches, further investigation is needed into their long-term safety and efficacy.

This multicenter, randomized, open-label, parallel-group, exploratory clinical trial aims to evaluate the impact of SAT-001, a Software as a Medical Device (SaMD), on choroidal thickness in pediatric patients. The study will compare changes in choroidal thickness between two groups: one receiving SAT-001 and the other receiving mSAT-001, a modified version of SAT-001 that excludes the rest period during device use. Participants will be assessed before and after a single application of the device.

Study Timeline

• Study Start: 2024-08-19
• Primary Completion: 2024-10-28
• Study First Submitted: 2024-12-04
• Study First Submitted QC: 2024-12-09
• Study First Posted: 2024-12-11
• Study Completion: 2024-12-31
• Status Verified: 2025-01
• Last Update Submitted: 2025-01-08
• Last Update Posted: 2025-01-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

1. Children aged 4 to 12

2. Meet the following refractive criteria by cycloplegic refraction

   1. Spherical equivalent refractive error (SER): -0.75 to less than -6.00 D in both eyes
   2. Astigmatism of 2.50 D or less in both eyes

3. Best corrected visual acuity of 0.2 logMAR or better in each eye at the Screening Visit

4. Gestational age of 38 weeks or more at birth, or birth weight of 2,500g or more

5. Transparent ocular media

6. Participants and their legal guardians who agree to participate in the clinical trial and are willing to provide signed informed consent after receiving and understanding the explanation of the trial description (participants under 6 years old may mark their agreement after receiving full information and understanding)

Exclusion Criteria

1. History of eye diseases such as manifest strabismus, intermittent strabismus, amblyopia, and nystagmus (excluding strabismus that maintains binocular vision)
2. History of ocular surgery such as eyelid surgery, strabismus surgery, intraocular surgery, or refractive correction surgery (excluding simple double eyelid surgery)
3. Ocular abnormalities in cornea, lens, central retina, iris, ciliary body, etc., or presence of malignant tumors in the orbital area
4. History of multifocal lenses (e.g., progressive lenses), corneal refractive therapy lenses (Ortho-K, e.g., Dream lenses), rigid gas permeable (RGP) hard lenses, defocus incorporated multiple segments (DIMS) spectacle lenses (e.g., MyoSmart) within 30 days prior to Visit 2.
5. History of using myopia control agents (e.g., atropine) within 30 days prior to Visit 2
6. Currently participating in another clinical trial or who have participated in another clinical trial within 3 months prior to screening (Visit 1)
7. Inappropriate at the discretion of the investigator due to potential ethical concerns or the possibility of affecting the clinical trial results

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Comparison of change in choroidal thickness from T0 to T1 (without device use) and from T1 to T2 (with device use) in Group 1	Baseline, 15 minute before device use, 15(mSAT-001 group) or 30(SAT-001 group) minutes after device use	Choroidal thickness will be measured using Optical Coherence Tomography (OCT) at five points: subfoveal, nasal, and temporal regions. The following comparisons will be made within Group 1: Change in Choroidal Thickness from Baseline (T0) to just before SAT-001 application (T1).; Change in Choroidal Thickness from just before SAT-001 application (T1) to after SAT-001 application (T2).; These changes will be evaluated and compared within Group 1.
Comparison of change in choroidal thickness change from T0 to T1 (without device use) and from T1 to T2 (with device use) in Group 2	Baseline, 15 minute before device use, 15(mSAT-001 group) or 30(SAT-001 group) minutes after device use	Choroidal thickness will be measured using Optical Coherence Tomography (OCT) at five points: subfoveal, nasal, and temporal regions. The following comparisons will be made within Group 2: Change in Choroidal Thickness from Baseline (T0) to just before mSAT-001 application (T1).; Change in Choroidal Thickness from just before mSAT-001 application (T1) to after mSAT-001 application (T2)
Comparison of change in choroidal thickness from T1 to T2 between Group 1 and Group 2	15 minute before device use, 15(mSAT-001 group) or 30(SAT-001 group) minutes after device use	Choroidal thickness will be measured using Optical Coherence Tomography (OCT) at five points: subfoveal, nasal, and temporal regions. The following comparison will be made: Comparison of Choroidal Thickness Change from pre- (T1) to post-treatment of application (T2) between Group 1 (SAT-001) and Group 2 (mSAT-001).

Trial Locations

Locations (2)

Hallym University Dongtan Sacred heart Hospital; 🇰🇷 Hwaseong-si, Korea, Republic of

Kangbuk Samsung Medical Center; 🇰🇷 Seoul, Korea, Republic of