Abstract
Current management of metabolic acidosis in patients with chronic kidney disease (CKD) relies on dietary intervention to reduce daily endogenous acid production or neutralization of retained acid with oral alkali (sodium bicarbonate, sodium citrate). Veverimer is being developed as a novel oral treatment for metabolic acidosis through removal of intestinal acid, resulting in an increase in serum bicarbonate. Veverimer is a free-amine polymer that combines high capacity and selectivity to bind and remove hydrochloric acid (HCl) from the gastrointestinal (GI) tract. In vitro studies demonstrated that veverimer had a binding capacity of 10.7 ± 0.4 mmol HCl per gram of polymer with significant binding capacity (>5 mmol/g) across the range of pH values found in the human GI tract (1.5-7). Upon protonation, veverimer bound chloride with high specificity but showed little or no binding of phosphate, citrate, or taurocholate (<1.5 mmol/g), which are all anions commonly found in the human GI tract. Administration of veverimer to rats with adenine-induced CKD and metabolic acidosis resulted in a significant increase in fecal chloride excretion and a dose-dependent increase in serum bicarbonate to within the normal range compared with untreated controls. Absorption, distribution, metabolism, and excretion studies in rats and dogs dosed with 14C-labeled veverimer showed that the polymer was not absorbed from the GI tract and was quantitatively eliminated in the feces. Acid removal by veverimer, an orally administered, nonabsorbed polymer, may provide a potential new treatment for metabolic acidosis in patients with CKD. SIGNIFICANCE STATEMENT: Metabolic acidosis is a complication of chronic kidney disease (CKD) as well as a cause of CKD progression. Veverimer is a high-capacity, selective, nonabsorbed, hydrochloric acid-binding polymer being developed as a treatment for metabolic acidosis. Veverimer binds and removes hydrochloric acid from the gastrointestinal tract, resulting in increased serum bicarbonate and the correction of metabolic acidosis. Veverimer is not an ion-exchange resin and does not deliver sodium or other counterions, and so it may be appropriate for patients with CKD with and without sodium-sensitive comorbidities.
Highlights
Metabolic acidosis is a common disorder in patients with non–dialysis-dependent, stage 3–5 chronic kidney diseaseThis work was supported in its entirety by Tricida, Inc
In vitro studies demonstrated that veverimer had a binding capacity of 10.7 6 0.4 mmol hydrochloric acid (HCl) per gram of polymer with significant binding capacity (.5 mmol/g) across the range of pH values found in the human GI tract (1.5–7)
Administration of veverimer to rats with adenine-induced chronic kidney disease (CKD) and metabolic acidosis resulted in a significant increase in fecal chloride excretion and a dose-dependent increase in serum bicarbonate to within the normal range compared with untreated controls
Summary
Metabolic acidosis is a common disorder in patients with non–dialysis-dependent, stage 3–5 chronic kidney disease. This work was supported in its entirety by Tricida, Inc. The authors report the following disclosures regarding their relationship and roles at Tricida, Inc. G.K. is a full-time Tricida employee and a member of the Tricida Board of Directors and has stock and stock options in Tricida; G.K. is listed on granted and pending Tricida patents. J.B. reports consulting fees and stock and stock options from Tricida during and outside this work; J.B. is listed on granted and pending Tricida patents. J.S., K.B., M.K., P.K., R.G., S.T., and S.N. are full-time Tricida employees and have stock and stock options in Tricida along with listings on granted and pending Tricida patents. The work was partially published in abstract form at American Society of Nephrology, Kidney Week 2019 (Washington, D.C.).
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