Comparison of iguratimod and conventional cyclophosphamide with sequential azathioprine as treatment of active lupus nephritis: study protocol for a multi-center, randomized, controlled clinical trial (iGeLU study)

Trials. 2021 Aug 11;22(1):530. doi: 10.1186/s13063-021-05475-3.

Abstract

Background: Systemic lupus erythematosus (SLE) is an autoimmune disease that can involve multiple organs or systems. Lupus nephritis (LN) is associated with high mortality and morbidity. However, plenty of patients do not respond to present treatment or relapse. Iguratimod (IGU) is a new small molecular, anti-rheumatic drug and has shown the potential for drug repurposing from rheumatoid arthritis (RA) to LN treatment. It has been approved for treating RA in northeast Asia. Beyond expectation in a recent observational study, over 90% of thirteen refractory LN patients responded to iguratimod monotherapy in 24 weeks, with no steroids dose increasing or any other medication add-on during the entire follow-up.

Methods/design: This study is a multi-center, randomized, 52-week parallel positive drug-controlled study. The study was designed as a head-to-head comparison between the iguratimod and present first-line therapy on LN patients. A total of 120 patients (60 patients each group) is in the enrolling plan. All enrolled patients are assigned randomly into trial and control groups. The patients will be selected from six study sites in China and will all have biopsy-proven active lupus nephritis. In the first 24 weeks of the trial, IGU is compared with cyclophosphamide as an induction therapy, and in the second 24 weeks, IGU is compared with azathioprine as a maintenance therapy. The primary outcome is renal remission rate including both complete remission and partial remission at week 52, which will be analyzed using a non-inferiority hypothesis test.

Discussion: Most patients diagnosed with SLE will develop LN within 5 years and LN remains a major cause of morbidity and death for SLE patients. Although some medications are proven effective for the treatment of this condition, at least 20-35% LN patients have to suffer from relapse or ineffective treatment and medication intolerance is also frequent. This trial is designed to demonstrate whether iguratimod can be used as an alternative induction or maintenance therapy in subjects who have lupus nephritis. Data from this study will provide an evidence on whether or not iguratimod should be recommended to active LN patients.

Trial registration: ClinicalTrials.gov NCT02936375 . Registered on October 18, 2016.

Keywords: Active lupus nephritis; Cyclophosphamide; Iguratimod; Randomized clinical trial; Systemic lupus erythematosus; treatment.

Publication types

  • Clinical Trial Protocol

MeSH terms

  • Azathioprine* / adverse effects
  • Chromones
  • Cyclophosphamide / adverse effects
  • Humans
  • Immunosuppressive Agents / adverse effects
  • Lupus Nephritis* / diagnosis
  • Lupus Nephritis* / drug therapy
  • Multicenter Studies as Topic
  • Randomized Controlled Trials as Topic
  • Remission Induction
  • Sulfonamides
  • Treatment Outcome

Substances

  • Chromones
  • Immunosuppressive Agents
  • Sulfonamides
  • iguratimod
  • Cyclophosphamide
  • Azathioprine

Associated data

  • ClinicalTrials.gov/NCT02936375