Phase 3 Uveitis Trial, Recruiting NCT06780462 Sponsor: Assistance Publique - Hôpitaux de Paris Condition: Uveitis
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Phase 3 Uveitis Trial, Recruiting

NCT06780462
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 18 years old or older
  • You have been diagnosed with Behçet's Syndrome (BS) based on recognised international diagnostic standards
  • You have been diagnosed with a deep vein blood clot (either for the first time or as a return of a previous clot), confirmed by an imaging scan such as an ultrasound, CT scan, or MRI
  • You are willing and able to sign a consent form agreeing to take part
  • If you are a woman who could become pregnant, you must have a negative pregnancy test before starting treatment and agree to use a reliable form of contraception throughout the trial (such as abstinence, hormonal contraception, an IUD, or other approved methods)
  • You are covered by a social security or health insurance system (including universal medical coverage)

Who may not be able to join:

  • You have another medical condition apart from your blood clot that requires you to take blood-thinning medication (for example, an irregular heartbeat called atrial fibrillation)
  • You are currently bleeding or are at high risk of bleeding, which would make blood-thinning treatment unsafe for you
  • You only have a clot in a surface vein (superficial vein) with no deeper clot involvement
  • You are currently pregnant or breastfeeding
  • You have been taking high-dose steroid tablets (more than 20mg of prednisone or equivalent daily for more than 6 weeks, or more than 4000mg of methylprednisolone in the 4 weeks before joining the trial)
  • You have already been taking blood-thinning medication for more than 4 weeks before joining the trial
  • You have severe long-term kidney problems (confirm with trial site) or serious liver disease that affects your blood's ability to clot
  • Your platelet count (cells that help blood clot) is too low (below a certain level — confirm with trial site)
  • Your treatment with biological therapy or immune-suppressing medication has been changed or had its dose adjusted in the month before joining the trial
  • You have a known allergy or medical reason that prevents you from safely taking corticosteroids (steroids) or a blood-thinning drug called Rivaroxaban
  • You are currently taking part in another clinical trial, or are still within a waiting period after finishing a previous trial

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

Phone: 0142178042

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 3
Registry
ClinicalTrials.gov
Start date
24 June 2025
Est. completion
24 December 2027

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Rate of success

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