Phase 4 Uveitis Trial, Recruiting NCT07663331 Sponsor: Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Condition: Uveitis
Back to Uveitis

Phase 4 Uveitis Trial, Recruiting

NCT07663331
Recruiting Phase 4

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 of age or older (any gender)
  • You have been diagnosed with active, non-infectious uveitis (inflammation inside the eye) affecting the middle, back, or entire eye, with signs of active inflammation confirmed by an eye doctor
  • You have been taking oral steroid tablets (such as prednisone) at a dose between 10 mg and 60 mg per day for at least 2 weeks before the screening visit, and are still on the same dose
  • You are willing to agree to not become pregnant, cause a pregnancy, or donate sperm during the entire trial and for 6 months after it ends, and will use effective contraception
  • Your doctor has assessed the risks and benefits and has prescribed you the study medication (adalimumab)
  • You are willing and able to sign a consent form agreeing to have your data collected and used for this study

Who may not be able to join:

  • You have certain types of eye conditions, such as: uveitis only at the front of the eye; suspected or confirmed eye infection; eye cancers (such as eye lymphoma); certain other specific eye diseases; significant cloudiness in the cornea or lens; very high eye pressure not well controlled by 2 or more glaucoma medications; very poor vision (below a certain level) in either eye; advanced diabetic eye disease; wet macular degeneration; or if you have had eye surgery within the past 90 days (some minor procedures may be exceptions — confirm with trial site)
  • You have, or have had in the past, a disease affecting the nerve coverings in the brain or spine (such as multiple sclerosis or optic neuritis)
  • You have, or have had, lupus (a disease where the immune system attacks the body)
  • You have a significant heart rhythm problem or moderate-to-severe heart failure
  • You have recently had a stroke or another serious medical condition that the doctor feels makes participation risky
  • You have or have had any cancer, except for certain successfully treated skin cancers or a very early-stage cervical condition (confirm with trial site)
  • You are allergic to the active ingredient in the study drug or similar medications
  • You have a body-wide inflammatory disease that requires ongoing steroid or immune-suppressing treatment
  • You have had a serious infection needing IV antibiotics in the last 30 days, or an infection needing oral antibiotics in the last 14 days
  • Your dose of certain immune-suppressing medications (such as methotrexate, cyclosporine, or others) was increased in the last 30 days, or your current doses are above set limits (confirm with trial site)
  • You received a live vaccine (such as MMR or chickenpox vaccine) within the past 3 months, or plan to receive one during the study
  • You received certain injections into the eye (such as anti-VEGF drugs like ranibizumab or aflibercept) within the past 90 days
  • You received a methotrexate injection into the eye within the past 90 days
  • You had a specific steroid eye implant (Ozurdex/dexamethasone implant) within the past 6 months
  • You have been treated with anti-TNF medications or certain other uveitis treatments within the past 6 months
  • You are currently taking part in another clinical trial
  • Your doctor does not feel it is appropriate or safe for you to participate

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 4 trials study a drug that has already been approved, monitoring long-term safety and effectiveness in real-world use.

Contact this trial

Phone: 15093292527

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 4
Sponsor
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
Registry
ClinicalTrials.gov
Start date
14 July 2026
Est. completion
1 February 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Time of treatment failure in subjects

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