Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02302079 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by Astellas Pharma Europe B.V..

Completed
Registry status
Phase 2
Development phase
96
Enrollment target

NCT02302079: Completed Phase 2 study, sponsored by Astellas Pharma Europe B.V..

NCT02302079 is a Phase 2 study that has completed, run by Astellas Pharma Europe B.V.. The registered enrollment target is 96 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (28% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02302079, a Phase 2 study, has completed, sponsored by Astellas Pharma Europe B.V..

COMPLETED
Registry status
Phase 2
Development phase
96 participants
Enrollment target

Study Summary

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.

Interventions

  • DRUG Placebo
  • DRUG ranibizumab
  • DRUG ASP8232
  • OTHER Sham intravitreal (IVT) injection

Trial Details

FieldValue
Enrollment Target 96 participants
Start Date 2015-01-12
Est. Completion 2016-08-12
Phase Phase 2
Astellas Pharma Europe B.V.

12 total trials

What the finished NCT02302079 record still lists

NCT02302079 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 96 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (28% lower).

The record links to 0 conditions, and to 4 interventions - of which Placebo is the first listed.

NCT02302079 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02302079 about?

NCT02302079 is a clinical study titled "A Study to Evaluate ASP8232 in Reducing Central Retinal Thickness in Subjects With Diabetic Macular Edema (DME)". 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...

What is the current status of trial NCT02302079?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 96 participants. The study started on 2015-01-12. Estimated completion is 2016-08-12.

What interventions are being tested in trial NCT02302079?

The interventions under investigation include: Placebo (DRUG), ranibizumab (DRUG), ASP8232 (DRUG), Sham intravitreal (IVT) injection (OTHER).

Who is sponsoring clinical trial NCT02302079?

This trial is sponsored by Astellas Pharma Europe B.V., which has 12 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02302079's enrollment target sits among peer trials

96 747th of 2000 higher than 1,242 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03401762 · 96 participants · NA

    Wearable MCI to Reduce Muscle Co-activation in Acute and Chronic Stroke

  • NCT03471260 · 96 participants · Phase 1

    Ivosidenib and Venetoclax With or Without Azacitidine in Treating Patients With IDH1 Mutated Hematologic Malignancies

  • NCT03549559 · 96 participants · NA

    Imaging Histone Deacetylase in the Heart

  • NCT03841058 · 96 participants · Phase 2

    Abaloparatide vs. Placebo in Post-Menopausal Women and Abaloparatide in Men Receiving Initial Spinal Fusion Surgery

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT02302079, the US trial registry maintained by the National Library of Medicine. NCT02302079 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.