Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
DS-2330b is an investigational **oral small-molecule inhibitor of sodium-dependent phosphate transporter 2b** developed by Daiichi Sankyo for the treatment of hyperphosphatemia in patients with chronic kidney disease, particularly those receiving hemodialysis. It is described in clinical-trial materials as a prodrug or formulated form associated with the free form DS2330a, and was studied as powder-in-bottle solution and tablet formulations administered three times daily. Mechanistically, it was intended to reduce intestinal phosphate absorption by inhibiting NaPi-IIb in the gut. In a phase 1b study in chronic hemodialysis patients, DS-2330b was reported to be generally safe and well tolerated alone or with sevelamer, but it did **not** demonstrate clinically meaningful phosphate-lowering efficacy, suggesting limited clinical utility in this indication.
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 DS-2330b.