The Efficacy and Safety of Calcitriol for the Treatment of Lupus Nephritis and Persistent Proteinuria

Last updated: July 31, 2015
Sponsor: Chinese University of Hong Kong
Overall Status: Trial Not Available

Phase

4

Condition

Cutaneous Lupus Erythematosus

Kidney Disease

Nephritis

Treatment

N/A

Clinical Study ID

NCT00508898
CRE-2007.261-T
  • Ages 18-65
  • All Genders

Study Summary

Glomerulonephritis and renal failure represent one of the most life-threatening manifestations of systemic lupus erythematosus (SLE). Although immunosuppressive therapy is often effective for the treatment of acute lupus nephritis, a significant proportion of patients show persistent proteinuria after resolution of the acute nephritic process, and develop progressive renal failure. There is preliminary evidence that calcitriol and other vitamin D analogs can reduce proteinuria in patients with chronic kidney diseases. The investigators plan to conduct a randomized control study to evaluate the safety and efficacy of calcitriol in the treatment of SLE patients with persistent proteinuria. Sixty patients with clinically quiescent SLE and persistent proteinuria despite conventional therapy will be recruited. They will be treated with calcitriol for 48 weeks. Proteinuria, renal function, lupus disease activity, serum and urinary inflammatory markers will be monitored. This study will explore the potential anti-proteinuric and immunomodulating effects of calcitriol in the treatment of SLE, which is a common and life threatening disease in young adults.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • aged 18-65 years

  • clinical quiescent SLE for at least 12 weeks

  • baseline SLEDAI score <= 4

  • history of biopsy-proven lupus nephritis

  • estimated glomerular filtration rate 15 to 60 ml/min/1.73m2

  • proteinuria > 1 g/day (or proteinuria > 1 g/g-Cr) in 2 consecutive samples within 12weeks despite ACE inhibitor or angiotensin receptor blocker for at least 3 months

  • on maintenance dose of prednisolone < 10 mg/day, with or without otherimmunosuppressive medications

  • corrected serum calcium level < 2.45 mmol/l

  • willingness to give written consent and comply with the study protocol

Exclusion

Exclusion Criteria:

  • Pregnancy, lactating or childbearing potential without effective method of birthcontrol

  • Severe gastrointestinal disorders that interfere with their ability to receive orabsorb oral medication

  • History of malignancy, including leukemia and lymphoma within the past 2 years

  • Systemic infection requiring therapy at study entry

  • Any other severe coexisting disease such as, but not limited to, chronic liverdisease, myocardial infarction, cerebrovascular accident, malignant hypertension

  • History of drug or alcohol abuse within past 2 years

  • Participation in any previous trial on vitamin D analogue

  • Patients receiving treatment of vitamin D and/or its analogue for other medicalreasons within the past 4 weeks. Patients who are taking multivitamin supplement thatcontains vitamin D could be enrolled after 4 weeks of wash out period by changing to apreparation that has no vitamin D.

  • On other investigational drugs within last 30 days

  • History of a psychological illness or condition such as to interfere with thepatient's ability to understand the requirement of the study

  • History of non-compliance

  • Known history of sensitivity or allergy to vitamin D analogs

Study Design

Study Start date:
May 01, 2008
Estimated Completion Date:
September 30, 2009