Ankylosing Spondylitis Trial, Recruiting NCT05835518 Sponsor: Yuhan Corporation Condition: Ankylosing Spondylitis
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Ankylosing Spondylitis Trial, Recruiting

NCT05835518
Recruiting Not Applicable

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 the ages of 19 and 75 (over 19 and under 75) at the time of signing up for the study
  • You have been diagnosed with rheumatoid arthritis (RA) or ankylosing spondylitis (AS) for at least 3 months before joining the study
  • Your doctor has decided that you should be prescribed the medication "Adalloce" as part of your treatment
  • You have never previously received the medication "Adalloce"
  • You are willing to voluntarily sign a consent form after being fully informed about the study's purpose and details

Who may not be able to join:

  • You have had an allergic reaction to Adalloce or any of its ingredients in the past
  • You currently have active tuberculosis, a serious infection such as blood poisoning (sepsis), or certain types of rare infections (opportunistic infections)
  • You have moderate to severe heart failure (confirm with trial site)
  • Your doctor determines that Adalloce is not appropriate for you based on the approved guidelines for this medication
  • The study doctor decides, for any reason, that it would not be suitable for you to take part
  • You are currently taking part in another clinical drug trial, or you are already participating in a post-marketing study of Adalloce

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
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Jeongyoon Choi, PI, Daegu Catholic University Medical Center

Phone: +82-2-828-0231

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
Not Applicable
Sponsor
Yuhan Corporation
Registry
ClinicalTrials.gov
Start date
26 January 2023
Est. completion
31 December 2025

Where this trial is recruiting

🇰🇷 South Korea

Primary endpoints

Changes in quality of life (EQ-5D-5L) scores at 52 weeks from baseline in patients with RA and AS

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