A Study of the VISION5 Product in Patients With Glaucoma or Ocular Hypertension
NCT01943721 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 14
Last updated 2014-12-17
Summary
The objective of this Phase 1 study is to evaluate the VISION5 Product's safety and efficacy.
Conditions
- Ocular Hypertension
- Primary Open Angle Glaucoma
Interventions
- DRUG
-
VISION5 Product
Sponsors & Collaborators
-
ForSight Vision5, Inc.
lead INDUSTRY
Principal Investigators
-
Anne Rubin · ForSight VISION5
Study Design
- Allocation
- NA
- Purpose
- PREVENTION
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2013-10-31
- Primary Completion
- 2014-06-30
- Completion
- 2014-06-30
Countries
- Latvia
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