Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
SBR759 is an oral, non-calcium, non-aluminum iron(III)-based phosphate binder developed for the treatment of hyperphosphatemia in patients with chronic kidney disease (CKD), particularly those receiving maintenance renal replacement therapy. The drug acts by binding dietary phosphate in the gastrointestinal tract to reduce serum phosphate levels. It is a complex formed from iron(III) chloride combined with potato starch, sucrose, and sodium carbonate. SBR759 demonstrated significant dose-dependent reductions in serum phosphate levels compared to placebo in clinical trials but was discontinued after phase II development for hyperphosphatemia. The drug was originally developed by SeBo GmbH and later by Novartis[1][2][3][6][8].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on SBR759.