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Completed Phase 2 Interventional

Efficacy and Safety of Squalamine Lactate Eye Drops in Subjects With Neovascular (Wet) Age-related Macular Degeneration (AMD)

ClinicalTrials.gov ID: NCT01678963

Public ClinicalTrials.gov record NCT01678963. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 26, 2026, 6:08 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase II Study of the Efficacy and Safety of Squalamine Lactate Ophthalmic Formulation 0.2% BID in Subjects With Neovascular AMD.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the safety and efficacy of topical ophthalmic squalamine lactate eye drops in treating patients with neovascular age-related macular degeneration (wet AMD), a degenerative retinal eye disease that causes a progressive, irreversible, severe loss of central vision.

Study identification

NCT ID
NCT01678963
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Ohr Pharmaceutical Inc.
Industry
Enrollment
142 participants

Conditions and interventions

Eligibility (public fields only)

Age range
50 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2012 (Type not available)
Primary completion
Mar 2015 (Actual)
Completion
Mar 2015 (Actual)
Last update posted
Jun 12, 2015

2012 – 2015

United States locations

U.S. sites
20
U.S. states
15
U.S. cities
20
Facility City State ZIP Site status
Retina Associates SW Tucson Arizona 85710 —
California Retinal Consultants Bakersfield California 93309 —
Retina-Vitreous Associates Beverly Hilss California 90211 —
Colorado Retina Golden Colorado 80401 —
Florida Eye Microsurgical Institute Inc. Boynton Beach Florida 33426 —
Retina Health Center Fort Myers Florida 33907 —
Midwest Eye Institute Indianapolis Indiana 46290 —
Elman Retina Baltimore Maryland 21237 —
Cumberland Valley Retina Consultants Hagerstown Maryland 21740 —
Ophthalmic Consultants of Boston Boston Massachusetts 02114 —
Vision Research Foundation Grand Rapids Michigan 49546 —
Vision Research Foundation Royal Oak Michigan 48073 —
Vision Research Foundation Traverse City Michigan 49686 —
Total Practice Management New Brunswick New Jersey 08901 —
Macula Care New York New York 10021 —
Retina Associates of Cleveland Cleveland Ohio 44122 —
PA Retina Camp Hill Pennsylvania 17011 —
TN Retina Nashville Tennessee 37203 —
Medical Center Ophthalmology Associates San Antonio Texas 78240 —
University of Wisconsin Madison Wisconsin 53705 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01678963, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 12, 2015 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01678963 live on ClinicalTrials.gov.

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