Phase III Clinical Study of Lifitegrast Ophthalmic Solution for the Treatment of Dry Eye Disease

Inclusion Criteria:

1. Voluntary participation and signing of the informed consent form, willingness tocomply with the treatment regimen prescribed by the trial protocol, and willingnessto attend follow-up visits on time.

2. Age ≥18 years, regardless of gender.

3. Best corrected visual acuity ≥4.3 in both eyes (OU) at the screening visit (V1visit).

4. History of dry eye disease in both eyes prior to the screening visit (V1 visit) (with at least one subjective symptom such as eye dryness, foreign body sensation,burning sensation, fatigue, discomfort, eye redness, or fluctuating vision).

5. Use of artificial tears within 30 days prior to the screening visit (V1 visit) toalleviate dry eye disease (DED) symptoms, with discontinuation of artificial tearsat least 72 hours prior to the screening period, and willingness to refrain fromusing artificial tears during the trial.

6. Total Ocular Surface Disease Index (OSDI) score ≥13 at the screening visit (V1visit).

7. Corneal fluorescein staining score ≥2 in at least one region of at least one eye andthe same eye at both the screening visit (V1 visit) and baseline visit (V2 visit).

8. Conjunctival hyperemia score ≥1 in at least one eye at both V1 and V2 visits.

9. Eye Dryness Score (EDS) ≥40 (VAS score, OU) at both V1 and V2 visits.

10. At least one eye and the same eye meeting the following criteria at both V1 and V2visits:

Inferior Corneal Fluorescein Staining Score (ICSS) ≥0.5; Schirmer's test (without anesthesia) ≥1 mm and ≤10 mm.- If both eyes meet the above criteria, the eye with the higher Inferior Corneal Fluorescein Staining Score (ICSS) at the V2 visit will be selected as the study eye. If both eyes have the same ICSS at the V2 visit, the eye with the lower Schirmer's Tear Test (STT) value at the V2 visit will be designated as the study eye. If both eyes have the same ICSS and STT values at the V2 visit, the right eye will be selected as the study eye.

Exclusion Criteria:

1. Currently suffering from ocular herpes or any other ocular infection orinflammation, or having a history of ocular herpes or any other ocular infectionwithin 30 days prior to screening.

2. Presence of eyelid margin structural abnormalities (ectropion, entropion, eyelidlaxity, etc.), severe conjunctivochalasis, Salzmann's nodular corneal degeneration,conjunctival goblet cell damage (e.g., vitamin A deficiency), progressive pterygium,wet age-related macular degeneration (wAMD), glaucoma, diabetic retinopathy, retinalvein occlusion, or other ocular diseases that, in the investigator's opinion, mayincrease the subject's risk or affect the trial results.

3. Ocular secondary scarring (e.g., radiation scars, chemical burns, Stevens-Johnsonsyndrome, cicatricial pemphigoid, etc.) that, in the investigator's opinion, mayaffect subject compliance or outcome assessment.

4. Subjects with secondary Sjögren's syndrome or other autoimmune diseases (e.g.,rheumatoid arthritis, systemic lupus erythematosus, etc.), unless the subject meetsthe following conditions: a. Not using corticosteroids, immunomodulatory, orimmunosuppressive drugs for the condition; b. The investigator considers that themedical condition will not affect the trial results.

5. History of organ or bone marrow transplantation.

6. Wearing contact lenses within 30 days prior to screening.

7. Undergoing physical treatments for dry eye (including eyelid scrubs, meibomian glandmassage, warm compresses, steam treatments, etc.) within 30 days prior to screening.

8. Use of aspirin or aspirin-containing medications, non-steroidal drugs (includingocular or systemic use), or medications that may cause dry eye (e.g.,anticholinergic drugs, serotonin reuptake inhibitors, etc.) within 30 days prior tothe baseline visit (V2 visit), unless the subject has been on a stable dose for atleast 30 days prior to the baseline visit and no change in dosage is expected duringthe trial.

9. Use of the following medications within the specified timeframes prior to thebaseline visit (V2 visit): a. Ocular or systemic antihistamines, any ocularmedications: within 14 days prior to V2 visit; b. Ocular cyclosporine, tacrolimus:within 6 weeks prior to V2 visit; c. Ocular or systemic corticosteroids, mast cellstabilizers: within 14 days prior to V2 visit.

10. History of punctal plug insertion or punctal cauterization within 12 weeks prior toscreening.

11. Use of anti-glaucoma medications within 3 months prior to screening, history ofnon-laser glaucoma surgery, or laser glaucoma surgery within 6 months prior toscreening.

12. History of YAG laser posterior capsulotomy within 6 months prior to screening, orcorneal refractive surgery (e.g., LASIK) within 12 months prior to screening.

13. Known allergy to fluorescein, multiple allergies, or severe allergic diseases.

14. Presence of other uncontrolled clinical conditions (e.g., severe chronic infections,severe cardiopulmonary diseases, uncontrolled hypertension [defined as systolicblood pressure ≥150 mmHg or diastolic blood pressure ≥100 mmHg despiteantihypertensive treatment], uncontrolled diabetes, malignancies, etc.).

15. Positive pregnancy test or lactating subjects (females only), or subjects ofchildbearing potential or male subjects with partners of childbearing potential whoare unwilling to use contraception during the study and for 1 month after the lastdose of study medication.

16. Participation in any other clinical trial involving investigational drugs/deviceswithin 30 days prior to screening.

17. Poor compliance during the placebo washout period (compliance <80% or >120%).

18. Other conditions deemed unsuitable for enrollment by the investigator (e.g.,depression, ocular mite infection, etc.). -