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Clinical proof-of-concept trial to assess the therapeutic effect of sirolimus in patients with autosomal dominant polycystic kidney disease: SUISSE ADPKD study

Andreas L Serra1 email, Andreas D Kistler1 email, Diane Poster1 email, Marian Struker1 email, Rudolf P Wüthrich1 email, Dominik Weishaupt2 email and Frank Tschirch2 email

1Clinic for Nephrology, University Hospital, CH-8091 Zürich, Switzerland

2Institute of Diagnostic Radiology, University Hospital, CH-8091 Zürich, Switzerland

author email corresponding author email

BMC Nephrology 2007, 8:13doi:10.1186/1471-2369-8-13

Published: 15 September 2007

Abstract

Background

Currently there is no effective treatment available to retard cyst growth and to prevent the progression to end-stage renal failure in patients with autosomal dominant polycystic kidney disease (ADPKD). Evidence has recently been obtained from animal experiments that activation of the mammalian target of rapamycin (mTOR) signaling pathway plays a crucial role in cyst growth and renal volume expansion, and that the inhibition of mTOR with rapamycin (sirolimus) markedly slows cyst development and renal functional deterioration. Based on these promising results in animals we have designed and initiated the first randomized controlled trial (RCT) to examine the effectiveness, safety and tolerability of sirolimus to retard disease progression in ADPKD.

Method/design

This single center, randomised controlled, open label trial assesses the therapeutic effect, safety and tolerability of the mTOR inhibitor sirolimus (Rapamune®) in patients with autosomal dominant polycystic kidney disease and preserved renal function. The primary outcome will be the inhibition of kidney volume growth measured by magnetic resonance imaging (MRI) volumetry. Secondary outcome parameters will be preservation of renal function, safety and tolerability of sirolimus.

Discussion

The results from this proof-of-concept RCT will for the first time show whether treatment with sirolimus effectively retards cyst growth in patients with ADPKD.

Trial registration

NCT00346918


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