Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Tenapanor is a small molecule inhibitor of the sodium/hydrogen exchanger isoform 3 (NHE3), primarily expressed on the apical surface of enterocytes in the small intestine and colon. By inhibiting NHE3, tenapanor reduces sodium absorption from the gut, leading to increased water retention in the intestinal lumen, softer stool consistency, and accelerated intestinal transit. It is approved for treating irritable bowel syndrome with constipation (IBS-C) and hyperphosphatemia associated with chronic kidney disease in adults on dialysis. Tenapanor also decreases visceral hypersensitivity and may reduce intestinal permeability by modulating tight junctions. The drug was developed by Ardelyx and is marketed under brand names including Ibsrela and Xphozah[1][2][4][5][6][7].
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 tenapanor.