A Study in Chinese Patients With Acquired Blepharoptosis

Launched by SANTEN PHARMACEUTICAL CO., LTD. · Nov 8, 2024

Keywords

ClinConnect Summary

This clinical trial is studying a new eye drop solution called STN1013800 to see if it can safely and effectively treat a condition known as acquired blepharoptosis, which causes drooping of the eyelids. Currently, there are no approved medications for this condition in China. The trial is specifically looking for Chinese patients aged 18 to 75 who have been diagnosed with acquired blepharoptosis and meet certain criteria regarding their vision and eyelid position.

Participants in the study will receive either the STN1013800 eye drops or a placebo (a treatment with no active medication) once a day for 42 days. Before joining, potential participants will go through a screening process to ensure they qualify. Throughout the trial, participants will have their vision and eyelid position assessed to see if the treatment is working. This trial is important because it could lead to a new treatment option for people suffering from this condition, improving their quality of life.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• * At least one eye diagnosed with acquired blepharoptosis and presence of all the following criteria at screening:
• • Loss of reliable Leicester Peripheral Field Test (LPFT) of ≥ 8 points in the top 2 rows (LPFT Eligibility Score); subjects had to see at least 9 total points in the top 4 rows (LPFT Total Score).
• • This criterion had to be met in both the Visit 1 Hour 0 (V1H0) and Visit 1 Hour 6 (V1H6) LPFT assessments.
• • There had to be ≤4 points of variance between the V1H0 and the V1H6 LPFT Eligibility Score.
• • The Marginal Reflex Distance-1 (MRD-1), the distance from the pupil center to the margin of upper lid, ≤ 2 mm (no visible pupil center defaults to 0) in the same eye
• • Visual acuity is 0.25 decimals (i.e., Snellen 20/80) or better according to standard logarithmic visual acuity chart in the same eye
• * Presence of all the following criteria at baseline:
• • Loss of reliable LPFT of ≥8 points in the top 2 rows (LPFT Eligibility Score) in the same eye; subjects had to see at least 9 total points in the top 4 rows (LPFT Total Score).
• • This criterion had to be met in the Visit 2 Hour 0 (V2H0) LPFT assessment
• • There had to be ≤4 points of variance between the V1H6 and the V2H0 LPFT Eligibility Score;
• • The MRD-1, the distance from the pupil center to the margin of upper lid, ≤ 2 mm (no visible pupil center defaults to 0) in the same eye
• • Visual acuity is 0.25 decimals (i.e., Snellen 20/80) or better according to standard logarithmic visual acuity chart in the same eye
• • Female subjects are 1-year postmenopausal, surgically sterilized, or females of childbearing potential (females who had started their menstrual cycles) with a negative urine pregnancy test at screening. Females of childbearing potential had to use an acceptable form of contraception throughout the study.
• • Exclusion Criteria: In the study eye
• • Dermatochalasis that extended less than 3 mm above the upper eyelid margin.
• • Pseudoptosis (upper eyelid dermatochalasis that overhung the upper eyelid margin).
• • In either eye: Congenital ptosis; Horner syndrome; Marcus Gunn jaw-winking syndrome; Myasthenia gravis.
• • Mechanical ptosis, including ptosis due to orbital or lid tumour, cicatricial processes affecting the movements of the upper lid, and enophthalmos.
• • Previous ptosis surgery (previous blepharoplasty \[only\] was allowed provided the surgery took place \> 3 months prior to screening).
• • Lid position affected by lid or conjunctival scarring; Visual field loss from any cause other than ptosis; History of herpes keratitis.
• • History of closed/narrow angle glaucoma (unless patent peripheral iridotomy had been performed \> 3 months prior to screening).
• • Periocular neurotoxin (e.g., Botox®, Dysport®) injections within 3 months prior to screening and during the study.
• • Topical application of bimatoprost (i.e., Latisse®) to the eyelashes within 7 days prior to screening and during the study.
• • Use of topical ophthalmic medications including but not limited to anti-allergy \[e.g., antihistamines like Emadine®, Patanol®\], dry eye \[e.g., Diquas®, Beifushu®; except artificial tears like Hyaluronate\], antimicrobial drugs \[e.g., antibiotics and antivirals like Cravit®,Tobrex®, Aciclovir\], and anti-inflammatory drugs
• • Current punctal plugs or placement of punctal plugs during the study.
• • Current use of over-the-counter (OTC) vasoconstrictor/decongestant eye medication or any ophthalmic or non-ophthalmic α-adrenergic agonist including OTC products at any time during the study.