A facilitated access open-label, non-randomized, multicenter, long-term safety and efficacy study in Chronic Kidney Disease patients treated with SBR759 who have completed previous SBR759 studies

Update Il y a 4 ans
Reference: EUCTR2009-011007-23

Woman and Man

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Extract

To evaluate long term safety data in patients who have completed a clinical study on SBR759 (ie: to provide long term safety and efficacy data on patients who have been titrated to achieve phosphate target within Phase II/III studies of SBR759 and completed these studies on SBR759. In addition, the study will provide access to continued SBR759 maintenance therapy for these patients. The study is an open-label, non-randomized design where patients will continue on their currently assigned dose from the previous SBR759 study)


Inclusion criteria

  • hyperphosphataemia in patients with chronic kidney disease (CKD) on haemodialysis