Therapeutic Effect of Hydroxychloroquine on Immunoglobulin A (IgA) Nephropathy Course QUIgAN Study
Condition(s) studied
Investigational drug(s) / intervention(s)
Hydroxychloroquine Oral Tablet: Active hydroxychloroquine once daily by oral route at 6.5 mg/kg of ideal weight/day, with maximal dose of 400mg/day for 3 years
Placebo oral tablet: placebo once daily by oral route (no active drug - same dosage as hydroxychloroquine )
Study summary
immunoglobulin A (IgA) nephropathy (Berger disease) is the most frequent primary glomerulonephritis worldwide. This disease accounts for about 5% of the causes of end stage renal disease in France, representing a major public health issue. Its pathophysiology seems to be triggered by mucosal immunity abnormalities leading to the systemic misaddressing of mucosal IgA, generation of circulating immunoglobulin A1 (IgA1) immune complexes finally deposited in renal glomeruli leading to renal tissue inflammation and scarring processes. Among this pathogeny, innate immunity is involved at several steps, including mucosal immunity.
In this regard, hydroxychloroquine has been shown to generate a global anti-inflammatory effect, particularly through its action on Toll like receptors and dendritic cells. This drug is well tolerated, widely used for other auto-immune diseases (e.g. Systemic Lupus Erythematosus) and very low priced.
One randomized controlled study conducted in China has recently shown a significant drop in proteinuria of IgA nephropathy patients treated with hydroxychloroquine (-48.4%) compared to the placebo group (+10.0%), after a quite short-term follow-up (6 months) and a moderate statistical power (30 patients in each group).
Considering (i) the potential mechanism of therapeutic effect on this disease, (ii) the well documented safety profile of the drug for rheumatologic indications and posologies, and its low cost (iii) its efficacy in reducing proteinuria in IgA nephropathy patients in a preliminary Chinese randomized control study, the investigators aim in this study at establishing the beneficial impact of hydroxychloroquine on IgA nephropathy in a double blind randomized controlled trial on a Caucasian French population with harder outcomes and a longer follow-up compared to the Chinese preliminary study.
Eligibility
Primary outcome measure(s)
- Absolute difference in estimate Glomerular Filtration Rate (GFR) between hydroxychloroquine group and control group evolution — 3 years
Trial sites (8)
| Facility | City | Region | Status |
|---|---|---|---|
| CHU Gabriel Montpied | Clermont-Ferrand | France | Recruiting |
| Hospices Civils de Lyon | Lyon | France | Recruiting |
| AP-HM Hôpital de la Conception | Marseille | France | Recruiting |
| Chr Metz Thionville Hopital Mercy | Metz | France | Recruiting |
| APHP Hôpital Bichat | Paris | France | Recruiting |
| APHP Hôpital de Tenon | Paris | France | Recruiting |
| CHU Lyon Sud | Pierre-Bénite | France | Recruiting |
| CHU de Saint-Etienne | Saint-Etienne | France | Recruiting |
More Centre Hospitalier Universitaire de Saint Etienne trials in France
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06350630 on ClinicalTrials.gov ↗ ← All trials in France