Phase 2 Uveitis Trial, Terminated NCT03207815 Sponsor: Gilead Sciences Condition: Uveitis
Back to Uveitis

Trial results

AI generated results summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

According to the results reported on ClinicalTrials.gov, this trial (NCT03207815) enrolled 74 people with active non-infectious uveitis (inflammation inside the eye not caused by infection) — 38 received filgotinib, an investigational oral medicine, and 36 received a placebo (a dummy pill with no active ingredient). The trial ran for up to 52 weeks and was primarily measuring how many participants in each group experienced what the researchers called "treatment failure" by week 24 — meaning their eye inflammation got worse or did not improve enough according to set criteria, such as new areas of inflammation appearing, inflammation scores not coming down to target levels, or vision worsening by a meaningful amount. The reported data shows that by week 24, 37.5% of participants in the filgotinib group met the criteria for treatment failure, compared with 67.6% in the placebo group. For the secondary measure of how quickly treatment failure occurred (from week 6 onward), the reported data shows a median time of 22.0 weeks in the placebo group; a median figure was not reported for the filgotinib group, which in this context means treatment failure did not occur in at least half of that group during the study period. For the remaining secondary measures — changes in eye inflammation scores (vitreous haze and anterior chamber cell grades), vision scores, and retinal thickness — small numerical changes were reported in both groups at week 52, but the data as submitted does not include the additional detail needed to describe meaningful differences between the groups for those measures. These are the results as reported to ClinicalTrials.gov. They are not medical advice — always discuss what they mean for you with your doctor.

These are the results as reported to ClinicalTrials.gov, not medical advice. Verify independently with the trial site and discuss what they mean for you with your doctor.

Phase 2 Uveitis Trial, Terminated

NCT03207815
Terminated Phase 2 🇦🇺 Australian site

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You have been diagnosed with a specific type of eye inflammation (uveitis) that is not caused by an infection, affecting the middle, back, or entire part of the eye
  • Your eye inflammation is still active at your first visit, meaning it has not fully responded after at least 2 weeks of taking a moderate dose of steroid tablets (such as prednisone)
  • You show at least one sign of ongoing inflammation in one eye, such as active lesions in the eye, or a certain level of inflammation detected during an eye exam (confirm with trial site for exact measurements)
  • You do not have active tuberculosis (TB), and any past or latent TB has already been treated

Who may not be able to join:

  • You have high pressure inside your eye and/or severe glaucoma
  • Your uveitis is caused or suspected to be caused by an infection, such as TB, cytomegalovirus, herpes, Lyme disease, toxoplasmosis, or several other infectious conditions

Important: Always verify eligibility with the trial site directly before applying.

Please note: There may be additional eligibility requirements beyond those listed here. The trial team will review your full medical history to determine whether this trial is right for you. This information is for general understanding only and is not medical advice.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Gilead Study Director, Gilead Sciences

Australian sites

Lions Eye Institute, Nedlands, Western Australia

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Terminated
Phase
Phase 2
Sponsor
Registry
ClinicalTrials.gov
Start date
26 July 2017
Est. completion
29 December 2020

Where this trial is recruiting

🇦🇺 Australia 🇨🇦 Canada 🇩🇪 Germany 🇮🇱 Israel 🇳🇿 New Zealand 🇬🇧 United Kingdom 🇺🇸 United States

1 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Percentage of Participants Failing Treatment for Active NonInfectious Uveitis by Week 24

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov