Phase 2 Uveitis Trial, Recruiting
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 intestinal Behçet's syndrome (a condition causing inflammation and ulcers in the gut) based on recognized international diagnostic criteria, confirmed by a camera examination of your bowel.
- Your symptoms are currently active and scored at a certain level of severity based on standard assessment tools (confirm with trial site).
- A bowel camera examination within the last 60 days has shown active ulcers in your intestine.
- You have already tried medium-to-high dose steroid tablets for over 1 month, or immune-suppressing medications for over 3 months, or biologic medicines for over 2 months, and your doctor considers these treatments to have failed or been poorly tolerated.
- Your current steroid dose is relatively low and has been stable for at least 2 weeks, and/or your immune-suppressing medication dose has been stable for at least 4 weeks.
- You understand what the study involves, are willing to take part, and are able to sign a consent form.
Who may not be able to join:
- You have been diagnosed with a different bowel condition such as Crohn's disease, ulcerative colitis, or lymphoma.
- You have serious active organ damage related to Behçet's syndrome — such as aneurysms (dangerous bulges in blood vessels), eye inflammation, or significant involvement of the brain or nervous system — that needs stronger immune-suppressing treatment right away.
- Your liver, kidney, or blood count results are significantly abnormal based on specific laboratory thresholds (confirm with trial site).
- You have an active infection such as active tuberculosis, active hepatitis B or C, syphilis, HIV, a long-term Epstein-Barr virus infection, an ongoing serious bacterial or viral infection, or a history of severe shingles.
- You have latent (inactive) tuberculosis and have not yet completed at least 3 weeks of preventative tuberculosis treatment before joining.
- You have a condition where your immune system does not work properly from birth (primary immunodeficiency).
- You have a history of cancer, or bowel tissue samples have shown early signs of cancer or abnormal cell changes.
- Your Behçet's syndrome never responded at all to a biologic medicine called infliximab (though people who responded but later stopped responding, or who could not tolerate it, may still be eligible).
- You have recently been treated with certain biologic or targeted medicines within specific timeframes depending on the medication — including infliximab, etanercept, tofacitinib, and several others (confirm with trial site for exact timeframes).
- You have previously used the medications baricitinib or adalimumab (ADA).
- You have complications of intestinal Behçet's syndrome such as a narrowed bowel causing symptoms, short bowel syndrome, a tunnel-like tract (fistula) in the bowel, or a suspected abscess in the abdomen; or you have had bowel surgery or other abdominal surgery within the last 6 months; or you have a functioning stoma or ostomy bag.
- You need to be fed through a drip or intravenous line because your illness is too severe to absorb nutrition normally.
- You are pregnant, breastfeeding, or planning to become pregnant in the near future.
- You are unable or unwilling to attend regular check-up visits as required by the study.
- You have a history of serious blood clot events or ongoing significant heart or blood vessel problems.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 86-10-69151188
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
Where this trial is recruiting
Primary endpoints
Proportion of patients with marked improvement (MI) at week 24 of follow-up
Can't join this trial?
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.