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Tenapanor Receives FDA Approval for Reducing Serum Phosphorous in CKD

On October 17, 2023, Ardelyx Inc announced the FDA approval of tenapanor (Xphozah) for reducing serum phosphorus in adults with chronic kidney disease on dialysis as add-on therapy. ....

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Approval at last: Ardelyx puts regulatory hitches to rest in US with long-sought CKD nod

“Finally!” Piper Sandler analysts cheered in a research note on Ardelyx Inc., which after spending three years battling the U.S. FDA, secured approval of Xphozah (tenapanor) for treating hyperphosphatemia in adults with chronic kidney disease (CKD). The company will waste no time getting to market, aiming to have the NHE3 inhibitor available to patients next month, marking the first new treatment class for hyperphosphatemia in 30 years. ....

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US FDA approves Ardelyx's kidney disease-related drug

Excess phosphorus can remove calcium from bones and other parts of the body, which in turn can cause brittle bones, joint pain, muscle cramps and itchy skin. The FDA has approved the drug for use in patients who have had an inadequate response or intolerance to phosphate binder therapies, the current standard-of-care treatment for the condition. ....

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Phosphate Binder Market Likely to Boost Future Growth by 2026 | Vifor Pharma, Cipla, Lupin

Phosphate Binder Market Likely to Boost Future Growth by 2026 | Vifor Pharma, Cipla, Lupin
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