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Completed Phase 2 Interventional

A Study to Evaluate ASP8232 in Reducing Central Retinal Thickness in Subjects With Diabetic Macular Edema (DME)

ClinicalTrials.gov ID: NCT02302079

Public ClinicalTrials.gov record NCT02302079. 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 21, 2026, 9:23 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 2, Double-Masked, Randomized, Active Controlled Study to Evaluate the Efficacy and Safety of ASP8232 in Reducing Central Retinal Thickness in Subjects With Diabetic Macular Edema

Brief summary

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

The purpose of this study is to evaluate efficacy and safety of ASP8232 in subjects with diabetic macular edema (DME). This study will evaluate the percent change from baseline in excess central subfield thickness (CST) in the study eye as assessed by spectral domain-optical coherence Tomography (SD-OCT) for ASP8232 monotherapy at Month 3.

Study identification

NCT ID
NCT02302079
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Astellas Pharma Europe B.V.
Industry
Enrollment
96 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 85 Years
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
Jan 12, 2015 (Actual)
Primary completion
Aug 12, 2016 (Actual)
Completion
Aug 12, 2016 (Actual)
Last update posted
Oct 31, 2024

2015 – 2016

United States locations

U.S. sites
21
U.S. states
11
U.S. cities
21
Facility City State ZIP Site status
Site US10021 Phoenix Arizona 85104 —
Site US10025 Tucson Arizona 85704 —
Site US10006 Arcadia California 91007 —
Site US10004 Beverly Hills California 90211 —
Site US10007 Palm Desert California 92260 —
Site US10011 Sacramento California 95819 —
Site US10031 Santa Ana California 92705 —
Site US10029 Golden Colorado 80401 —
Site US10016 Miami Florida 33126 —
Site US10005 Winter Haven Florida 33880 —
Site US10036 Augusta Georgia 30909 —
Site US10002 Boston Massachusetts 02114 —
Site US10001 Omaha Nebraska 985540 —
Site US10027 Reno Nevada 89511 —
Site US10012 Nashville Tennessee 37203 —
Site US10010 Abilene Texas 79606 —
Site US10015 Austin Texas 78705 —
Site US10013 Houston Texas 77030 —
Site US10030 McAllen Texas 78503 —
Site US10009 San Antonio Texas 78240-1502 —
Site US10017 Charlottesville Virginia 22903 —

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 NCT02302079, 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 Oct 31, 2024 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02302079 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →