Phase 3 Uveitis Trial, Not Yet Recruiting NCT06925698 Sponsor: Marmara University Condition: Uveitis
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Phase 3 Uveitis Trial, Not Yet Recruiting

NCT06925698
Not Yet Recruiting Phase 3

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 are between 18 and 50 years old.
  • You have been diagnosed with Behçet's Disease using the standard international diagnostic criteria (ISG criteria).
  • You have not previously had blood vessel complications from Behçet's Disease, or you have not been treated with immune-suppressing medicines for blood vessel complications.
  • You have been diagnosed with a blood clot in a vein in your leg or lower body within the last 14 days before joining the study.
  • Your blood clot has been confirmed by ultrasound, a special X-ray (venography), CT scan, or MRI scan showing specific signs of a clot.
  • If you are a woman who could become pregnant, you must not be pregnant or breastfeeding, and you must be using effective birth control, be past menopause (no periods for at least 1 year), or have had a surgical procedure to prevent pregnancy.
  • You are able to give written consent and follow the study's requirements.

Who may not be able to join:

  • You have any abnormal bulging of a blood vessel (aneurysm) anywhere in your body.
  • You have another serious long-term illness besides Behçet's Disease.
  • You have previously had a bad reaction or intolerance to the medication Rivaroxaban.
  • You have taken immune-suppressing medicines (such as azathioprine, cyclosporine, or certain biological medicines) within the last 6 months.
  • You have taken steroid medicines (such as cortisone) for more than 3 months for Behçet's Disease skin or mouth symptoms.
  • You have already received blood-thinning injections (such as heparin) for more than 48 hours, or more than one dose of warfarin-type medicines, before joining the study.
  • You have already had a procedure to remove the clot, a filter placed in a large vein, or clot-dissolving treatment for your current clot.
  • You are planning to receive a live vaccine within 30 days of joining the study.
  • You have a significant uncontrolled illness affecting the heart, lungs, liver, kidneys, blood, gut, nerves, or an active infection or cancer that could affect the study results.
  • You are due to have surgery or have another medical condition that the study doctor feels makes you unsuitable for the trial.
  • You have had cancer in the last 5 years (with some exceptions for certain minor skin cancers or early-stage cervical changes — confirm with trial site).
  • Your kidneys are not working well enough (confirmed by a blood test showing low kidney filtration rate below 30 ml/min).
  • You have serious liver disease, such as hepatitis or cirrhosis, or abnormal liver blood test results.
  • You are actively bleeding or are at high risk of bleeding, which would make blood-thinning treatment unsafe for you.
  • Your blood pressure is very high and not under control (above 180/110 mmHg).
  • You have severe anaemia (low red blood cell levels, confirmed by a blood test).
  • You are pregnant, breastfeeding, or a woman of childbearing age not using contraception.
  • You are taking certain strong medications that affect how the body processes Rivaroxaban (such as some HIV medicines, systemic ketoconazole, rifampin, carbamazepine, or phenytoin).
  • You have taken part in another clinical drug trial within the last 30 days.
  • Your life expectancy is less than 3 months.
  • You have had a serious infection in the last 60 days, such as a heart valve infection, tuberculosis, or other opportunistic infections.
  • You are currently misusing alcohol or substances, or have had a substance dependence problem within the last year.
  • You have tested positive for Hepatitis B, Hepatitis C, or HIV.
  • You have a known blood clotting disorder or significant abnormal blood test results (confirm with trial site).
  • You have had suicidal behaviour in the last 6 months, or have had serious thoughts of suicide in the last 2 months (confirm with trial site).

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 3: approximately ~65% 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: Fatma Alibaz-Oner, Prof, Marmara University

Phone: +90 216 625 45 45

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
Not Yet Recruiting
Phase
Phase 3
Sponsor
Marmara University
Registry
ClinicalTrials.gov
Start date
30 April 2025
Est. completion
1 April 2027

Where this trial is recruiting

Turkey (Türkiye)

Primary endpoints

Rate of Thrombotic Relapse at 52 Weeks

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