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Completed

NCT Number: NCT02949349

Mycophenolate Mofetil Versus Azathioprine for Maintenance Therapy of Lupus Nephritis

This study is designed to compare the safety and efficacy of Mycocep Capsules (Mycophenolate Mofetil) and a marketed Azathioprine formulation, Imuran Azathioprine Tablets, in the maintenance therapy of lupus nephritis.

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Key information

About this study

This study is designed to compare the two different doses of Mycocep Capsules (1.0g/day & 1.5g/day) and Imuran Azathioprine Tablets (2mg/kg/day), all in combination with low-dose prednisolone (≤10mg/day) as maintenance treatment for lupus nephritis.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of lupus nephritis.
  • Currently receiving maintenance therapy with Azathioprine, Mycophenolate Mofetil, Mycophenolate Sodium, or Cyclosporine for lupus nephritis for at least 3 months prior to randomization.
  • Stable use of low dose (≤10mg/day) oral prednisolone for lupus nephritis for at least 3 months prior to randomization.

Exclusion criteria

  • Untreated, not in need of immunosuppressive treatment (in addition to corticosteroids), currently receiving induction therapy, or not responding to Azathioprine, Mycophenolate Mofetil or Mycophenolate Sodium as induction or maintenance therapy for lupus nephritis.
  • Currently receiving or anticipated to receive cyclophosphamide or IV pulse of corticosteroids.
  • Currently receiving continuous dialysis starting more than 2 weeks before randomization, and/or with an anticipated duration of more than 8 weeks.
  • Previous kidney transplant or planned transplant.
  • Presence of life threatening complications such as cerebral lupus or severe infection.
  • Presence of liver dysfunction.
  • Presence of COPD or asthma requiring oral steroids.
  • Presence of bone marrow insufficiency or pure red cell aplasia unrelated to active systemic lupus erythematosus.
  • Presence of persistent hematuria or pyuria for causes other than lupus nephritis.

Treatment and study plan

Mycophenolate mofetil

Drug

Provided as 250mg/capsule, dose specific for each arm, orally twice a day, for 24 weeks.

Other names: Mycocep Capsules

azathioprine

Drug

Provided as 50mg/tablet, 1mg/kg, orally twice a day, for 24 weeks.

Other names: Imuran Azathioprine Tablets

Prednisolone

Drug

Daily dose not more than 10mg, orally, for 24 weeks.

Primary outcomes

  1. Change in serum albumin

    Time frame: 24 weeks treatment

  2. Change in serum creatinine

    Time frame: 24 weeks treatment

  3. Change in spot urine protein/creatinine ratio

    Time frame: 24 weeks treatment

Secondary outcomes

  1. Change in serum albumin

    Time frame: 12 weeks treatment

  2. Change in serum creatinine

    Time frame: 12 weeks treatment

  3. Change in spot urine protein/creatinine ratio

    Time frame: 12 weeks treatment

  4. Change in cholesterol

    Time frame: 24 weeks treatment

  5. Change in triglyceride

    Time frame: 24 weeks treatment

  6. Change in complete blood count/differential count (CBC/DC)

    Time frame: 24 weeks treatment

  7. Change in number of subjects with doubling of serum creatinine

    Time frame: 24 weeks treatment

  8. Change in the average daily dose of oral prednisolone

    Time frame: 24 weeks treatment

Sponsors and collaborators

Lead sponsor

Genovate Biotechnology Co., Ltd.,

Industry

Registry information

Important dates

Study start
2015
Primary completion
2016
Study completion
2017
First posted
Oct 31, 2016
Registry last updated
Mar 3, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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