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Clinical trialNCT02251938CompletedPhase 3Interventional

A Phase IIIb, Multinational, Multicenter, Open-Label Extension Study Assessing the Long-Term Safety of PRN Intravitreal Injections of DE-109 in Subjects With Non-Infectious Uveitis of the Posterior Segment of the Eye Who Have Participated in the SAKURA Development Program

SponsorSanten Inc.Enrollment60Non-Infectious Uveitis of the Posterior Segment of the Eye
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The objective of this extension study is to evaluate the long-term safety of treatment with DE-109 (440 μg) in subjects with non-infectious uveitis of the posterior segment of the eye who have participated in the SAKURA development program.

Investigators

The overall officials registered on this study. Names that resolve to a FindMyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

25 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Austria
  • Facility name not stated

    Graz, Austria

France
  • Facility name not stated

    Paris, France

India
  • Facility name not stated

    Hyderabad, Andhra Pradesh, India

  • Facility name not stated

    Aurobindo Marg, New Dehli, India

  • Facility name not stated

    Daryāganj, New Dehli, India

  • Facility name not stated

    Bhubaneswar, Odisha, India

  • Facility name not stated

    Chennai, Tamil Nadu, India

  • Facility name not stated

    Madurai, Tamil Nadu, India

  • Facility name not stated

    Noida, Uttar Pradesh, India

Italy
  • Facility name not stated

    Milan, Italy

Turkey (Türkiye)
  • Facility name not stated

    Ankara, Turkey (Türkiye)

  • Facility name not stated

    Izmir, Turkey (Türkiye)

United States
  • Facility name not stated

    Phoenix, Arizona, United States

  • Facility name not stated

    Sacramento, California, United States

  • Facility name not stated

    Golden, Colorado, United States

  • Facility name not stated

    Tampa, Florida, United States

  • Facility name not stated

    Oak Park, Illinois, United States

  • Facility name not stated

    Jackson, Michigan, United States

  • Facility name not stated

    St Louis, Missouri, United States

  • Facility name not stated

    New Brunswick, New Jersey, United States

  • Facility name not stated

    Palisades Park, New Jersey, United States

  • Facility name not stated

    New York, New York, United States

  • Facility name not stated

    Orchard Park, New York, United States

  • Facility name not stated

    Austin, Texas, United States

  • Facility name not stated

    Salt Lake City, Utah, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

DE-109 440 μg
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
29 Sept 2014
Primary completion
1 Nov 2017
Completion
27 Nov 2017
Last update posted
12 Feb 2020
Registered enrollment
60
Registry id
NCT02251938

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 4 Nov 2026. Registry facts are shown as registered by the study sponsor; FindMyKOL does not interpret them.