CompletedPhase 4

Study to Evaluate OXERVATE® in Patients With Stage 1 Neurotrophic Keratitis

United States37 participantsStarted 2020-09-09

Plain-language summary

This study is to evaluate the safety and efficacy of OXERVATE® 0.002% (20 mcg/mL) cenegermin-bkbj ophthalmic solution in patients with Stage 1 neurotrophic keratitis (NK).

Who can participate

Age range18 Years

SexALL

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Inclusion criteria

✓. Male or female aged ≥ 18 years.
✓. Patients with Stage 1 NK defined by the Mackie criteria

Exclusion criteria

✕. Evidence of an active ocular infection (bacterial, viral, protozoal) in either eye.
✕. Have current or history of conditions that may confound the study data including but not limited to Ocular Cicatricial Pemphigoid (OCP), Graft Versus Host Disease (GVHD), neuromyelitis optica, uncontrolled dry eye, and Steven Johnson's syndrome.
✕. History of severe systemic allergy or severe ocular allergy (including seasonal conjunctivitis expected during the subject's participation in the trial) or chronic conjunctivitis and/or keratitis other than dry eye disease.
✕. Patients with severe vision loss with no potential for visual improvement in the study eye, in the opinion of the investigator, or if the subject is deemed legally blind.
✕. Ocular surgery or elective ocular surgery expected during participation in the trial.
✕. Patients with eyelid abnormality that may alter eyelid function including but not limited to Blepharospasm, Cerebrovascular accident, entropion, ectropion, floppy lid syndrome.

What they're measuring

Corneal Epithelial Healing

Timeframe: Week 8

Trial details

NCT IDNCT04485546

SponsorDompé Farmaceutici S.p.A

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2021-09-30

Results submitted2023-05-22

View on ClinicalTrials.gov More Neurotrophic Keratitis trials