Overview

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

Status:
Recruiting
Trial end date:
2021-08-01
Target enrollment:
0
Participant gender:
All
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).
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Dompé Farmaceutici S.p.A
Collaborator:
Dompé US
Treatments:
Ophthalmic Solutions
Criteria
Inclusion Criteria:

1. Male or female aged ≥ 18 years.

2. Patients with Stage 1 NK defined by the Mackie criteria

Exclusion Criteria:

1. Evidence of an active ocular infection (bacterial, viral, protozoal) in either eye.

2. 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.

3. 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.

4. 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.

5. Ocular surgery or elective ocular surgery expected during participation in the trial.

6. Patients with eyelid abnormality that may alter eyelid function including but not
limited to Blepharospasm, Cerebrovascular accident, entropion, ectropion, floppy lid
syndrome.