Ardelyx Announces Four Abstracts Accepted for Poster Presentations at the American Society of Nephrology’s Kidney Week
Ardelyx (Nasdaq: ARDX) announced four poster presentations supporting XPHOZAH (tenapanor) at the American Society of Nephrology Kidney Week, November 5–9, 2025 in Houston.
XPHOZAH is described as the first and only phosphate absorption inhibitor approved by the U.S. FDA to reduce serum phosphorus in adults with CKD on dialysis as add-on therapy for patients with inadequate response or intolerance to phosphate binders; it is dosed as a single tablet twice daily.
Four posters will present real-world effectiveness, treatment satisfaction, bowel-movement benefits, and trends in etelcalcetide use and parathyroidectomy rates on November 6–7, 2025, plus an Exhibitor Spotlight on November 7, 2025 from 11:00–11:45 AM CST.
Ardelyx (Nasdaq: ARDX) ha annunciato quattro poster presentation a sostegno di XPHOZAH (tenapanor) durante la Kidney Week dell'American Society of Nephrology, dal 5 al 9 novembre 2025 a Houston.
XPHOZAH è descritto come il primo e unico inibitore dell'assorbimento del fosfato approvato dalla FDA per ridurre il fosforo sierico negli adulti con CKD in dialisi come terapia add-on per pazienti con risposta inadeguata o intolleranza ai leganti del fosfato; è dosato come una singola compressa due volte al giorno.
Quattro poster presenteranno efficacia nel mondo reale, soddisfazione del trattamento, benefici sulle evacuazioni intestinali e tendenze nell'uso di etelcalcetide e nei tassi di paratiroidectomia dal 6 al 7 novembre 2025, oltre a un Exhibitor Spotlight il 7 novembre 2025 dalle 11:00 alle 11:45 CST.
Ardelyx (Nasdaq: ARDX) anunció cuatro presentaciones de pósteres en apoyo de XPHOZAH (tenapanor) en la Kidney Week de la American Society of Nephrology, del 5 al 9 de noviembre de 2025 en Houston.
XPHOZAH se describe como el primer y único inhibidor de la absorción de fosfato aprobado por la FDA de EE. UU. para reducir el fósforo sérico en adultos con ECV en diálisis como terapia adicional para pacientes con respuesta inadecuada o intolerancia a los quelantes de fosfato; se dosifica como una tableta única dos veces al día.
Cuatro pósteres presentarán efectividad en el mundo real, satisfacción con el tratamiento, beneficios en las deposiciones y tendencias en el uso de etelcalcetide y tasas de paratiroidectomía entre el 6 y 7 de noviembre de 2025, además de un Exhibitor Spotlight el 7 de noviembre de 2025 de 11:00 a 11:45 CST.
Ardelyx (나스닥: ARDX)은 미국 신장학회 Kidney Week 2025에서 XPHOZAH (tenapanor)를 지지하는 네 편의 포스터 발표를 Houston에서 2025년 11월 5–9일에 발표했습니다.
XPHOZAH는 혈청 인을 감소시키기 위해 미국 FDA가 승인한 최초이자 유일한 인 흡수 억제제로, CKD 환자의 투석 치료에 대한 보조 요법으로 사용되며, 반응 미흡 또는 불내증이 있는 환자에 적합합니다. 복용량은 하루에 두 번, 한 알씩의 단일 정제로 투여합니다.
여러 포스터에서는 2025년 11월 6–7일에 실제 세계에서의 효과, 치료 만족도, 배변 이점, etelcalcetide 사용 추세 및 부갑상샘 절제술 비율에 대해 다루며, 2025년 11월 7일에는 11:00–11:45 CST에 Exhibitor Spotlight가 있습니다.
Ardelyx (Nasdaq: ARDX) a annoncé quatre affiches soutenant XPHOZAH (tenapanor) lors de la Kidney Week de l'American Society of Nephrology, du 5 au 9 novembre 2025 à Houston.
XPHOZAH est décrit comme le premier et unique inhibiteur d'absorption du phosphate approuvé par la FDA pour réduire le phosphore sérique chez les adultes atteints d'IRC en dialyse, en tant que thérapie d'appoint pour les patients présentant une réponse insuffisante ou une intolérance aux binders de phosphate; il se dose sous forme d'un seul comprimé deux fois par jour.
Quatre affiches présenteront l'efficacité dans le monde réel, la satisfaction du traitement, les bienfaits sur les selles et les tendances dans l'utilisation d'etelcalcetide et les taux de parathyroïdectomie les 6 et 7 novembre 2025, ainsi qu'un Exhibitor Spotlight le 7 novembre 2025 de 11h00 à 11h45 CST.
Ardelyx (Nasdaq: ARDX) kündigte vier Posterpräsentationen zur Unterstützung von XPHOZAH (Tenapanor) während der Kidney Week der American Society of Nephrology vom 5. bis 9. November 2025 in Houston an.
XPHOZAH wird als erster und einziger Phosphat-Aufnahmehemmer beschrieben, der von der US-FDA zugelassen ist, um den Phosphorspiegel bei Erwachsenen mit CKD auf Dialyse als Zusatztherapie für Patienten mit unzureichender Reaktion oder Unverträglichkeit gegenüber Phosphatbindern zu senken; es wird als eine einzelne Tablette zweimal täglich verabreicht.
Vier Poster werden realweltliche Wirksamkeit, Behandlungszufriedenheit, Stuhlbefunde und Trends bei der Verwendung von Etelcalcetide sowie Raten von Parathyroidektomien am 6. bis 7. November 2025 vorstellen, sowie am 7. November 2025 von 11:00–11:45 Uhr CST ein Exhibitor Spotlight geben.
أعلنت Ardelyx (ناسداك: ARDX) عن أربع عروض بوسترات تدعم XPHOZAH (تينابنور) في Kidney Week لجمعية أمراض الكلى الأمريكية، من 5 إلى 9 نوفمبر 2025 في هيوستن.
يوصف XPHOZAH بأنه أول وأوحّد مثبِّط لامتصاص الفسفات معتمد من إدارة الغذاء والدواء الأمريكية لتقليل الفوسفور في الدم لدى البالغين المصابين بأمراض الكلى المزمنة على الغسيل كعلاج إضافي للمرضى الذين لديهم استجابة غير كافية أو تحمل غير جيد لمثبطات الفسفور؛ يتم تناولها كقرص واحد مرتين يوميًا.
ستعرض أربعة بوسترات الفعالية الواقعية، ورضا العلاج، وفوائد حركة الأمعاء، واتجاهات استخدام ايتيلكالسيتيِد (etelcalcetide) ونسب الاستئصال الجار درقي في 6-7 نوفمبر 2025، بالإضافة إلى Exhibitor Spotlight في 7 نوفمبر 2025 من 11:00-11:45 صباحًا بتوقيت CST.
Ardelyx (纳斯达克: ARDX) 宣布在美国肾脏病学会 Kidney Week(2025年11月5日–9日,休斯顿)期间,为 XPHOZAH(十酸羟)提供四场海报展示。
XPHOZAH 被描述为美国 FDA 批准的第一种也是唯一一种磷吸收抑制剂,用于降低慢性肾病(CKD)透析成人的血清磷水平,作为对磷结合剂反应不足或耐受性差患者的辅助治疗;它以单次一粒、每日两次的剂量给药。
四场海报将于 2025 年 11 月 6–7 日展示真实世界的有效性、治疗满意度、肠道运动的益处,以及 etelcalcetide 使用趋势和甲状旁腺切除术率,并且在 2025 年 11 月 7 日 11:00–11:45 CST 举行 Exhibitor Spotlight。
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WALTHAM, Mass., Oct. 21, 2025 (GLOBE NEWSWIRE) -- Ardelyx, Inc. (Nasdaq: ARDX), a biopharmaceutical company founded with a mission to discover, develop and commercialize innovative, first-in-class medicines that meet significant unmet medical needs, today announced upcoming data presentations supporting XPHOZAH® (tenapanor) at the American Society of Nephrology’s Kidney Week, to be held November 5-9, 2025, in Houston.
XPHOZAH, the first and only phosphate absorption inhibitor (PAI), is approved by the U.S. Food and Drug Administration to reduce serum phosphorus in adults with chronic kidney disease (CKD) on dialysis as add-on therapy in patients who have an inadequate response to phosphate binders or who are intolerant of any dose of phosphate binder therapy. XPHOZAH offers a different mechanism of action that blocks phosphate absorption at the primary pathway and is administered as a single tablet taken twice daily.
Information regarding ASN's Kidney Week, including copies of presentation abstracts, can be found here.
Ardelyx Poster Presentations:
Title: Real-World Effectiveness of Tenapanor (XPHOZAH) for Treatment of Hyperphosphatemia in United States Patients on Dialysis
Authors: Alan J. Fossa, Dhajanae Sylvertooth, Angelo Karaboyas, Brian Bieber, Roberto Pecoits-Filho, David Rosenbaum, Laura Williams, Luisa Scott
Poster Number: TH-PO0221
Date/Time: November 6, 2025, from 10:00 AM – 12:00 PM CST
Title: Treatment Satisfaction with Tenapanor (XPHOZAH): Real-World Survey of Patients with End-Stage Renal Disease and Hyperphosphatemia
Authors: Jessica Kendrick, Luisa Scott, Belinda Gist, Laura Williams
Poster Number: TH-PO0224
Date/Time: November 6, 2025, from 10:00 AM – 12:00 PM CST
Title: Tenapanor Improves Bowel Movements in Patients with End-Stage Kidney Disease and Mild to Severe Constipation
Authors: Steven Fishbane, Suling Zhao, Yang Yang, Susan Edelstein, David M. Spiegel
Poster Number: TH-PO0223
Date/Time: November 6, 2025, from 10:00 AM – 12:00 PM CST
Title: Etelcalcetide Utilization Rates Decreased and Parathyroidectomy Rates Increased Following the Incorporation of Calcimimetics into the End-Stage Kidney Disease Bundle
Authors: Brian Bieber, Angelo Karaboyas, Roberto Pecoits-Filho, Kevin Martin, Stuart Sprague
Poster Number: FR-PO0254
Date/Time: November 7, 2025, from 10:00 AM – 12:00 PM CST
In addition to the poster presentations during ASN’s Kidney Week, Ardelyx is sponsoring an Exhibitor Spotlight: “Expanding Perspectives in Hyperphosphatemia Treatment; A Different Approach” on November 7, 2025, from 11:00 – 11:45 AM CST, where José A Morfin, MD, FASN, will discuss the first and only phosphate absorption inhibitor with a different non-binder mechanism. Participants can learn about its clinical data, safety, practical considerations, patient cases, and more.
About XPHOZAH® (tenapanor)
XPHOZAH, discovered and developed by Ardelyx, is a first-in-class, phosphate absorption inhibitor with a differentiated mechanism of action that acts locally in the gut to inhibit the sodium hydrogen exchanger 3 (NHE3), thereby reducing phosphate absorption through the paracellular pathway, the primary pathway of phosphate absorption. XPHOZAH is a single tablet, taken twice daily. Diarrhea was the most common side effect experienced by patients taking XPHOZAH in clinical trials. Please see additional full Prescribing Information.
About Hyperphosphatemia
Hyperphosphatemia is a serious condition, defined as elevated levels of phosphate in the blood, which affects the vast majority of the 550,000 patients in the United States with chronic kidney disease (CKD) on maintenance dialysis. The kidneys are responsible for eliminating excess phosphate and as kidney function declines, phosphate is not adequately eliminated from the body. As a result, hyperphosphatemia is a nearly universal condition among people with CKD on maintenance dialysis, with internationally recognized KDIGO treatment guidelines that recommend lowering elevated phosphate levels toward the normal range (2.5-4.5mg/dL).
IMPORTANT SAFETY INFORMATION
CONTRAINDICATIONS
XPHOZAH is contraindicated in:
- Pediatric patients under 6 years of age
- Patients with known or suspected mechanical gastrointestinal obstruction
WARNINGS AND PRECAUTIONS
Diarrhea
Patients may experience severe diarrhea. Treatment with XPHOZAH should be discontinued in patients who develop severe diarrhea.
MOST COMMON ADVERSE REACTIONS
Diarrhea, which occurred in 43
INDICATION
XPHOZAH (tenapanor), 30 mg BID, is indicated to reduce serum phosphorus in adults with chronic kidney disease (CKD) on dialysis as add-on therapy in patients who have an inadequate response to phosphate binders or who are intolerant of any dose of phosphate binder therapy.
For additional safety information, please see full Prescribing Information.
About Ardelyx
Ardelyx was founded with a mission to discover, develop and commercialize innovative, first-in-class medicines that meet significant unmet medical needs. Ardelyx has two commercial products approved in the United States, IBSRELA® (tenapanor) and XPHOZAH® (tenapanor). Ardelyx has agreements for the development and commercialization of tenapanor outside of the U.S. Kyowa Kirin commercializes PHOZEVEL® (tenapanor) for hyperphosphatemia in Japan. A New Drug Application for tenapanor for hyperphosphatemia has been approved in China with Fosun Pharma. Knight Therapeutics commercializes IBSRELA in Canada. For more information, please visit https://ardelyx.com/ and connect with us on X (formerly known as Twitter), LinkedIn and Facebook.
Investor and Media Contacts:
Lindsey Manuel
lmanuel@ardelyx.com
