Phase 4 Interstitial Lung Disease Trial, Not Yet Recruiting NCT07643038 Sponsor: Chinese SLE Treatment And Research Group Condition: Interstitial Lung Disease
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Phase 4 Interstitial Lung Disease Trial, Not Yet Recruiting

NCT07643038
Not Yet 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 have been diagnosed with rheumatoid arthritis (RA) based on standard medical criteria.
  • A special lung scan (called an HRCT) has shown that you have a type of lung scarring or inflammation called interstitial lung disease (ILD), affecting at least 20% of your lungs, and other causes such as infection or fluid buildup have been ruled out.
  • Your lung function tests show that your lungs are not working at full capacity — specifically, your breathing capacity or ability to absorb oxygen is below certain levels.
  • If you are currently taking steroid medication (such as prednisone), you have been on a low, stable dose of no more than 10 mg per day for at least 4 weeks before the study starts.
  • If you are currently taking a type of disease-modifying medication (called a csDMARD), you have been on a stable dose for at least 4 weeks before the study starts.
  • You are willing and able to give written consent and attend all required study visits and follow-up appointments.

Who may not be able to join:

  • You have another autoimmune disease in addition to rheumatoid arthritis.
  • You have a serious, uncontrolled medical condition affecting a major organ that the study doctor believes would put you at too much risk.
  • You have had a cancer diagnosis within the past 5 years.
  • You are currently pregnant, breastfeeding, or planning to become pregnant or breastfeed during the study.
  • You have a known allergy or sensitivity to any of the study medications (tocilizumab, telitacicept, or methotrexate) or their ingredients.
  • You currently have an active hepatitis B, hepatitis C, tuberculosis, or shingles infection, or you have had a serious infection requiring hospital care or IV antibiotics within the past 12 weeks.
  • Your blood protein levels (albumin or IgG antibodies) are very low (confirm with trial site).
  • Certain liver or kidney function blood test results are outside of acceptable ranges (confirm with trial site).
  • You have taken part in another clinical trial involving a treatment within the past 4 weeks.
  • You are unable to complete the lung function tests or other assessments required by the study.
  • The study doctor has any other concern that makes participation unsuitable for you.

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 27 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

Principal Investigator: Xinping Tian, Peking Union Medical College Hospital

Phone: +86-13691165939

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 4
Sponsor
Chinese SLE Treatment And Research Group
Registry
ClinicalTrials.gov
Start date
1 July 2026
Est. completion
31 July 2029

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Change in FVC from baseline to week 52

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: 27 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