Phase 2 Uveitis Trial, Recruiting NCT06849908 Sponsor: Peking Union Medical College Hospital Condition: Uveitis
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Phase 2 Uveitis Trial, Recruiting

NCT06849908
Recruiting Phase 2

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.

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

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

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
8 November 2024
Est. completion
30 June 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Proportion of patients with marked improvement (MI) at week 24 of follow-up

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