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Recruiting NCT07406932

A Study on the Efficacy and Safety of JAK Inhibitors Versus Calcineurin Inhibitors as Initial Therapy for Interstitial Lung Disease Associated With Antisynthetase Syndrome

No phase Interventional Antisynthetase Syndrome Interstitial Lung Disease (ILD)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: JAK Inhibitor, Calcineurin Inhibitors (CNI).
Who it may be relevant to
Registry conditions: Antisynthetase Syndrome, Interstitial Lung Disease (ILD). Basic parameters: 18 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This study is a prospective investigation comparing the efficacy and safety of Janus kinase inhibitors versus calcineurin inhibitors as initial therapy for interstitial lung disease associated with antisynthetase syndrome. The goal is to determine which treatment is more effective at improving lung function and preventing disease progression, while comparing their safety profiles. The findings will help provide clearer treatment guidance for doctors and patients.

Detailed description

This is a single-center, randomized, open-label, prospective study. Eligible adults with interstitial lung disease associated with antisynthetase syndrome (ASS-ILD) who are treatment-naïve will be randomly assigned to receive either a JAK inhibitor (tofacitinib 5 mg twice daily, or baricitinib 4 mg once daily, or upadacitinib 15 mg once daily) or a calcineurin inhibitor (tacrolimus 0.075 mg/kg/day in two divided doses, or cyclosporine 2-5 mg/kg/day in two divided doses), both in combination with a standard glucocorticoid regimen. The primary endpoint is the 12-month survival rate. Secondary endpoints include changes in lung function, high-resolution CT (HRCT) scores, glucocorticoid dosage reduction, and the proportion of patients achieving low disease activity. Safety and laboratory parameters will be closely monitored throughout the 12-month treatment and follow-up period. Statistical analyses will compare the efficacy and safety profiles between the two treatment arms, and subgroup analyses will be performed to explore potential predictors of treatment response.

Interventions

  • Drug JAK Inhibitor
    Oral JAK inhibitors (tofacitinib 5 mg twice daily, or baricitinib 4 mg once daily, or upadacitinib 15 mg once daily) administered in combination with standard glucocorticoid therapy for 12 months.
  • Drug Calcineurin Inhibitors (CNI)
    Oral calcineurin inhibitors (tacrolimus 0.075 mg/kg/day in two divided doses, or cyclosporine 2-5 mg/kg/day in two divided doses) administered in combination with standard glucocorticoid therapy for 12 months.

Primary outcome measures

  • 12-month survival rate [Time frame: 12 months]
Secondary outcome measures (4)
  • Annual decline rate of lung function (FVC% and DLCO%) [Time frame: Change from baseline to 12 months]
  • Change in HRCT score [Time frame: Change from baseline to 12 months]
  • Rate of glucocorticoid tapering [Time frame: Over 12 months]
  • Proportion of patients achieving low disease activity (LDA) [Time frame: At 6 months and 12 months]

Eligibility criteria

Inclusion criteria

  • Age 18 to 75 years.
  • Meet the 2017 EULAR/ACR diagnostic criteria for Anti-synthetase Syndrome (ASS).
  • Presence of Interstitial Lung Disease (ILD) confirmed by High-Resolution Computed Tomography (HRCT).
  • Active disease requiring initiation or intensification of immunosuppressive therapy, with no prior use of glucocorticoids, immunosuppressants, or biologics.
  • Signed informed consent form.

Exclusion criteria

  • Diagnosis of Rapidly Progressive ILD (RP-ILD), defined as worsening dyspnea within 1 month and PaO2/FiO2 ratio < 250 mmHg.
  • Active uncontrolled severe infection, malignancy, or major organ failure.
  • Pregnancy or lactation.
  • Contraindications to the study drugs.
  • Concurrent use of other immunosuppressants or biologics.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

China · 1 center
  • China-Japan Friendship Hospital — Beijing

Identifiers

NCT: NCT07406932 · JAKCNIASSILD

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗