Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Veverimer is a first-in-class, orally administered, non-absorbed polymer developed for the treatment of metabolic acidosis in patients with chronic kidney disease (CKD)[1][2][3][5]. It is composed of crosslinked, high-molecular-weight polyamines and acts as a hydrochloric acid binder in the gastrointestinal tract[1][6][7]. Upon ingestion, veverimer becomes protonated and selectively binds chloride anions, sequestering hydrochloric acid (HCl) from the stomach. This process leads to increased serum bicarbonate concentrations without introducing exogenous cations such as sodium or potassium[2][5][6]. The HCl-bound polymer is excreted in feces. Veverimer has demonstrated efficacy in raising serum bicarbonate levels and improving physical function in CKD patients with metabolic acidosis during clinical trials; however, it has not received FDA approval as of 2024 due to requests for additional data on clinical benefit[3][5].
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 veverimer.