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Motugivatrep may be well tolerated at 1 year
Patients receiving the treatment alone or alongside existing therapies showed sustained improvements in dry eye symptoms and ocular surface findings in a 52-week phase 3 study.
Assess the 52-week safety and clinical outcomes of motugivatrep 0.3% ophthalmic suspension, used alone or with existing dry eye therapies, in adults with dry eye disease.
Approach:
Design and participants: Multicenter, open-label, single-arm phase 3 study at 22 clinics in Japan; 162 adults enrolled and 149 completed treatment.
Treatment: Participants used one drop in each eye four times daily for 52 weeks. Of these, 105 received motugivatrep alone and 57 received it with diquafosol sodium, rebamipide, or sodium hyaluronate.
Assessments: Primary outcomes were the incidence and severity of treatment-emergent and treatment-related adverse events. Assessments also included patient-reported symptoms and ocular surface measures.
Key Findings:
Treatment-emergent adverse events occurred in 73 patients (45%); treatment-related adverse events occurred in 24 (15%). Most treatment-related events were mild, and none were severe or serious.
Three patients had serious adverse events, all judged unrelated to treatment; no deaths occurred. Three patients discontinued because of adverse events, including one with treatment-related events.
Patient-reported symptoms improved early and remained below baseline through week 52. Mean DEQS total score decreased by 22.18 points from a baseline of 37.61.
Corneal fluorescein staining and conjunctival staining improved, and tear break-up time increased. Tear secretion decreased from baseline.
The authors reported no clinically meaningful changes in ophthalmic examinations, vital signs, or laboratory measures.
Interpretation:
The authors reported that motugivatrep 0.3% used four times daily was well tolerated over 52 weeks, with clinical outcomes consistent with a treatment effect when used alone or with standard dry eye therapies.
Limitations:
The open-label, single-arm design had no concurrent placebo or active comparator, so symptom improvements cannot be definitively attributed to motugivatrep.
Unmasked symptom assessments and possible effects of medication washout before baseline may have influenced observed changes.
Participants were enrolled in Japan, and most had relatively mild corneal staining at baseline, which may limit generalizability.
Combination-therapy subgroups were small, and the study was not designed to compare treatment approaches.