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Completed Phase 1 Interventional

Phase 1 Study of Topical Ocular PAN-90806 for Neovascular AMD

ClinicalTrials.gov ID: NCT02022540

Public ClinicalTrials.gov record NCT02022540. 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 30, 2026, 5:31 PM EDT

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

Official title

A Phase I Open-Label, Multi-Center Trial With Randomization to Dose to Evaluate the Safety and Tolerability of Topical Ocular PAN-90806 in Patients With Neovascular Age-Related Macular Degeneration (AMD)

Brief summary

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

The objective of this study is to assess the safety and tolerability of topical ocular PAN-90806 in patients with active, subfoveal choroidal neovascularization associated with neovascular Age-Related Macular Degeneration (AMD).

Study identification

NCT ID
NCT02022540
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
PanOptica, Inc.
Industry
Enrollment
50 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
Feb 2014 (Type not available)
Primary completion
Mar 2016 (Actual)
Completion
May 2016 (Actual)
Last update posted
Sep 28, 2016

2014 – 2016

United States locations

U.S. sites
22
U.S. states
14
U.S. cities
22
Facility City State ZIP Site status
Not listed Colorado Springs Colorado — —
Not listed Winter Haven Florida — —
Not listed Shawnee Mission Kansas — —
Not listed Wichita Kansas — —
Not listed Boston Massachusetts — —
Not listed Portsmouth New Hampshire — —
Not listed Bloomfield New Jersey — —
Not listed Charlotte North Carolina — —
Not listed Durham North Carolina — —
Not listed Statesville North Carolina — —
Not listed Ashland Oregon — —
Not listed Philadelphia Pennsylvania — —
Not listed West Columbia South Carolina — —
Not listed Rapid City South Dakota — —
Not listed Nashville Tennessee — —
Not listed Abilene Texas — —
Not listed Austin Texas — —
Not listed Harlingen Texas — —
Not listed McAllen Texas — —
Not listed San Antonio Texas — —
Not listed Willow Park Texas — —
Not listed Madison Wisconsin — —

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 NCT02022540, 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 Sep 28, 2016 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02022540 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →