Phase 1 Study for Safety and Tolerability of EBI-005 Topically Administered to Eyes of Healthy Adult Subjects
Completed · Phase 1 · Has a placebo group
Conditions studied: Dry Eye
In brief
This is a First-In-Human (FIH) study to assess the safety and tolerability of ocular administration of EBI-005 in healthy volunteers. Additionally, the PK and immunogenicity of EBI-005 will be assessed.
Key facts
- Study ID
- NCT01748578
- Run by
- Eleven Biotherapeutics
- People needed
- 16
- Starts
- 2012-11-01
- Expected to finish
- 2013-03-01
- Last updated by the study team
- 2013-05-08
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy adult males and/or females between the ages of 18 and 65 years
- Medically healthy
- Best correction vision of greater than or equal to 20/40 in each eye
- Non-tobacco/nicotine-containing product users for a minimum of 6 months prior to dosing
- Tolerate topical administration to eye
- Signed and dated, Institutional Review Board (IRB) approved informed consent form (ICF) prior to any protocol-specific screening procedures
You may not qualify if…
- History or presence of significant cardiovascular, pulmonary, hepatic, renal, hematological, gastrointestinal, endocrine, immunologic, dermatologic (including sensitive skin on the face), neurological, or psychiatric disease, or any other clinically significant disease not deemed acceptable by the PI
- History of any primary malignancy, with the exception of basal cell or squamous cell carcinomas of the skin or cervical carcinoma in situ or other malignancies curatively treated and with no evidence of disease for at least 5 years
- Occurrence of active seasonal allergies including ocular allergies (e.g.; annual hay fever)
- Abnormalities following ophthalmological examination: abnormality of the cornea, evidence of ocular inflammation (dry eyes, blepharitis, allergic conjunctivitis, iritis, and uveitis), glaucoma, and optic neuropathy
- Subjects with a history of laser refractive surgery (laser assisted stromal in-situ keratomileusis [LASIK], photorefractive keratectomy [PRK]), radial keratotomy (RK), corneal transplantation, dry eyes, or radiotherapy to the eyes
- Use of contact lenses currently or within the past one year
- Positive urine drug/alcohol or cotinine testing
Where it is running
- Celerion — Tempe, Arizona, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.