| Eligibility |
---Inclusion Criteria ---
1. 18 to 75 years of age (inclusive) at the time of signing the ICF, either sex or ethnic
group.
2. With history of dry eye for at least 6 months prior to screening, and history of use
or willingness to use eye drops for the treatment of dry eye within 6 months prior to
screening
.
3. Binocular BCVA = 0.25 decimals (standard logarithmic visual acuity chart) at Screening
and Baseline.
4. At least one eye (the same eye) meets all the following criteria at screening and
baseline:
- TCSS = 2 points
- Eye dryness score (EDS) = 40 points in VAS
- Conjunctival hyperemia score = 1 point
- TFBUT = 5 seconds
- 1 mm/5 min = Schirmer I test (without surface anesthesia) = 10 mm/5 min
5. Must be able to understand and sign the ICF approved by Independent Ethics Committee
(EC).
6. Willing and able to conduct protocol-required study visits, follow study guidelines,
and take study drug as instructed.
---Exclusion Criteria ---
1. With contraindication or hypersensitivity to the study drug (OT202 and excipients) or
diagnostic reagents (fluorescein sodium, lissamine green, etc.).
2. During the screening period and baseline period, any eye with ocular active
inflammation or structural abnormalities that may affect the trial assessment,
including but not limited to trichiasis, blepharospasm, blepharitis, meibomitis,
severe meibomian gland dysfunction, bulbar conjunctival laxity, keratitis, recurrent
corneal erosion, allergic conjunctivitis, iritis, anterior chamber inflammation, known
retinal detachment, diabetic retinopathy, or history of any progressive retinal
disease.
3. With history of possible or confirmed ocular infection (bacterial, viral, or fungal)
or ocular herpes (simple or zoster) in either eye, as determined by the patient's
medical history and/or at the screening and baseline examinations.
4. Those with intraocular pressure (non-contact tonometry) greater than 21 mmHg or less
than 8 mmHg or diagnosed with glaucoma at screening and baseline, or those with ocular
hypertension who underwent intraocular pressure reduction therapy, and those with a
history or suspicion of glaucoma.
5. Those with any systemic disease expected to potentially affect the study results. It
include but is not limited to Sjögren syndrome, Stevens-Johnson syndrome, rheumatoid
arthritis, graft versus host disease, systemic lupus erythematosus, scleroderma,
sarcoidosis, herpes, acne, rosacea, etc.
6. Those who cannot stop using any ocular medication or treatment during the clinical
trial.
7. Those with recent clinically relevant history (e.g., hepatic, renal impairment) within
6 months prior to screening or current severe, unstable, or uncontrolled
cardiovascular, pulmonary, hepatic, renal, autoimmune, and other relevant systemic
diseases (e.g., severe chronic obstructive pulmonary disease, arrhythmia, significant
heart failure, uncontrolled hypertension, type 2 diabetes mellitus), as assessed by
the investigator.
8. Those on a chronic, systemic medication regimen used for less than 1 month at
screening and baseline or with dose changed within 1 month (including initiation of
new medication and discontinuation).
9. Those who have used any prohibited medications (topical ocular, systemic, and/or
injectable medications) during the specified period prior to screening. These
medications are also prohibited during the study. However, if a subject has a
prohibited medication at screening, it needs to be stopped and washed out according to
the washout period specified below, which can be included in the wash-out period. The
minimum reasonable washout period for prohibited medications is as follows:
- Systemic and local immunosuppressant and immunotherapy (such as cyclosporine eye
drops, tacrolimus eye drops, etc.): 60 days;
- Corticosteroids (any route): 14 days;
- Systemic or ocular topical mast cell stabilizers, antihistamines,
antihistamines/mast cell stabilizer combination, vasoconstrictors, monoamine
oxidase inhibitors: 7 days;
- Other topical ophthalmic preparations (including artificial tears): 3 days;
- Medications known to cause ocular dryness (e.g., anticholinergics, serotonin
reuptake inhibitors, beta-blockers, diuretics, etc.): 14 days.
Note:Non-periocular, low-potency, over-the-counter corticosteroid topical skin creams
are allowed for use in the study (e.g., hydrocortisone butyrate cream/ointment).
10. Previous use of spleen tyrosine kinase (Syk) inhibitors or eye drop products targeting
the same as anti-vascular endothelial growth factor (VEGF).
11. Those who wore corneal contact lenses within 7 days prior to screening or required
them during the study.
12. Those who underwent meibomian gland massage or moist chamber therapy within 7 days
prior to screening, or non-drug therapies for dry eye such as intense pulsed light
therapy, thermal pulsation therapy, etc., within the previous 6 months before
screening.
13. Those who previously underwent dry eye surgery such as tear duct embolization (current
tear duct embolization status or punctal plug use in the past 6 months) or amniotic
membrane transplantation.
14. Those who underwent ocular surface surgery (e.g., LASIK excimer laser in situ
keratomileusis) within 12 months prior to screening or intraocular surgery within 6
months prior to screening in either eye, as determined by the subject's medical
history and/or examination, or anticipated ocular surgery during the study.
15. Those who use other investigational products or devices within 3 months prior to
screening or concurrently during the study.
16. Non-compliance with drug administration (< 80% or > 120%) during the introduction
period.
17. Females of childbearing potential who are currently pregnant, or have a positive
pregnancy test result, or plan to get pregnant during the study, or are currently
breastfeeding, or do not agree to use appropriate contraception methods to avoid
pregnancy during the study period up to 1 month after the last dose of study drug.
18. Males who do not agree to use one or more acceptable effective contraception methods
during the study period up to 1 month after the last dose of study drug.
19. Any condition or situation that, in the opinion of the investigator, may pose a safety
risk to the subject in the trial or may interfere with the conduct of the study, or
the investigator believes that the subject may not be able to complete or comply with
the requirements of the study (due to administrative reasons or otherwise).
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