Effect of NOV03 on Signs and Symptoms of Dry Eye Disease Associated With Meibomian Gland Dysfunction (Mojave Study)

Completed · Phase 3

Conditions studied: Dry Eye Disease

In brief

The objectives of this trial are to assess the efficacy, safety, and tolerability of NOV03 ophthalmic solution in comparison to a saline control for the treatment of the signs and symptoms of Dry Eye Disease (DED) associated with Meibomian Gland Dysfunction (MGD).

Key facts

Study ID: NCT04567329
Run by: Bausch & Lomb Incorporated
People needed: 620
Starts: 2020-11-18
Expected to finish: 2021-08-30
Last updated by the study team: 2024-08-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Was at least 18 years of age at the time of consent.
Provided written informed consent.
Had a subject-reported history of DED in both eyes for at least 6 months prior to Visit 0.
Had a TFBUT ≤5 seconds at Visit 0 and Visit 1.
Had an OSDI score ≥25 at Visit 0 and Visit 1.
Had an unanesthetized Schirmer's test I score ≥5 mm at Visit 0 and Visit 1.
Had MGD defined as total MGD score ≥3 at Visit 0 and Visit 1 (secretion of 5 central glands on the lower eyelid was evaluated, and each was scored from 0-3: 0 = normal; 1 = thick/yellow, whitish, particulate; 2 = paste; 3 = none/occluded). Total score ranged from 0-15.
Had a tCFS score between 4 and 11 (ie, sum of inferior, superior, central, nasal, and temporal) according to the NEI scale at Visit 0 and Visit 1.
Had at least one eye (the same eye) that satisfied all criteria for 4, 6, 7, and 8 above at Visit 0 and Visit 1.
Was able and willing to follow instructions, including participation in all trial assessments and visits.

You may not qualify if…

A subject was excluded from participating in the study if he or she met any of the following criteria:
Had been randomized in NVU-002 or NVU-003 study or had participated in the NVU-004 open-label extension (OLE) study.
Had any clinically significant ocular surface slit-lamp findings at Visit 0 and Visit 1 and/or in the opinion of the Investigator had any findings that may have interfered with trial parameters, including eye trauma or history of eye trauma or anterior membrane dystrophy.
Had a history of Stevens-Johnson syndrome.
Had active blepharitis or lid margin inflammation that required any topical antibiotics or topical steroids within last 30 days prior to Visit 0 or would have likely required such treatment during the trial. Any other lid margin therapy such as lid scrubs, lid wipes, warm compresses, systemic antibiotics (such as tetracyclines) and oral supplements for treatment of ocular conditions had to be stable within the last 30 days prior to Visit 1 and was to be maintained throughout the trial.
Had had a LipiFlow procedure, intense pulse light procedure or any kind of other procedure affecting meibomian glands within 6 months prior to Visit 1.
Had abnormal lid anatomy that caused incomplete eyelid closure, including entropion and ectropion, or floppy lid syndrome that exposed parts of the conjunctiva or impaired the blinking function of the eye.
Had received or removed a permanent punctum plug within 3 months (6 months for dissolvable punctum plugs) prior to Visit 1 or was expected to receive a punctum plug or removal of a punctum plug, or had a punctum plug expected to be dissolved during the trial.
Had DED secondary to scarring, irradiation, alkali burns, cicatricial pemphigoid, or destruction of conjunctival goblet cells (as with vitamin A deficiency).
Had an ocular or periocular malignancy.
Had a corneal epithelial defect or had significant confluent staining or filaments anywhere on the cornea.
Had a history of herpetic keratitis.
Had active ocular allergies or ocular allergies that were expected to be active during the trial period.
Was diagnosed with an active ocular or systemic infection (bacterial, viral, or fungal), including fever requiring treatment with antibiotics.
Had worn contact lenses within 1 month of Visit 0 or anticipated using contact lenses during the trial.
Had used any eye drops and/or TrueTearTM device (intranasal tear neurostimulator) within 24 hours before Visit 1.
Had undergone intraocular surgery or ocular laser surgery within the previous 6 months or had any planned ocular and/or lid surgeries over the trial period.
Was a family member living in the same household as another subject who was randomized into Study 904 or NVU-003 or participated in NVU-004 OLE.
Was a clinical site employee directly involved in the management, administration, or support of this trial or was an immediate family member of the same.
Was a woman who was pregnant, nursing or planning a pregnancy.
Was unwilling to submit to a urine pregnancy test at Visit 0, Visit 1 and Visit 4 (or early termination visit) if of childbearing potential. Non-childbearing potential was defined as a woman who was permanently sterilized (eg, had a hysterectomy or bilateral tubal ligation or bilateral oophorectomy) or was post-menopausal (without menses for 12 consecutive months).
Was a woman of childbearing potential who was not using an acceptable means of birth control; acceptable methods of contraception included: hormonal (oral, implantable, injectable, or transdermal contraceptives); mechanical (spermicide in conjunction with a barrier such as a diaphragm or condom); intrauterine device; or surgical sterilization of partner. For non-sexually active females, abstinence could have been regarded as an adequate method of birth control; however, if the subject became sexually active during the trial, she had to agree to use adequate birth control as defined above for the remainder of the trial.
Had an uncontrolled systemic disease in the opinion of the Investigator.
Had a known allergy and/or sensitivity to the investigational drug or saline components.
Had active ocular or periocular rosacea that in the judgement of the Investigator interfered with the trial (eg, clinically relevant lid induration).

Where it is running

Bausch Site 206 — Phoenix, Arizona, United States
Bausch Site 202 — Garden Grove, California, United States
Bausch Site 221 — Hemet, California, United States
Bausch Site 214 — Inglewood, California, United States
Bausch Site 226 — Murrieta, California, United States
Bausch Site 213 — Santa Ana, California, United States
Bausch site 236 — Westminster, California, United States
Bausch site 225 — Grand Junction, Colorado, United States
Bausch Site 211 — Delray Beach, Florida, United States
Bausch Site 204 — Morrow, Georgia, United States
Bausch Site 209 — Chicago, Illinois, United States
Bausch site 218 — Hoffman Estates, Illinois, United States
Bausch Site 230 — Overland Park, Kansas, United States
Bausch Site 207 — Louisville, Kentucky, United States
Bausch Site 228 — Havre de Grace, Maryland, United States
Bausch Site 231 — Bloomington, Minnesota, United States
Bausch Site 229 — St Louis, Missouri, United States
Bausch Site 224 — St Louis, Missouri, United States
Bausch Site 217 — Washington, Missouri, United States
Bausch Site 208 — Rochester, New York, United States
Bausch Site 210 — Asheville, North Carolina, United States
Bausch site 233 — High Point, North Carolina, United States
Bausch site 232 — Southern Pines, North Carolina, United States
Bausch Site 201 — Cincinnati, Ohio, United States
Bausch Site 216 — Cleveland, Ohio, United States

Full record on ClinicalTrials.gov

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