COMPANY
Ardelyx
Hiring
| Title | Location (from posting) | Employer posted | First seen |
|---|---|---|---|
| Area Business Director (Gastroenterology) - Los Angeles, CA | Los Angeles, California | Not stated | Oct 23, 2026 |
| Associate Director, Market Access Training | 2 locations (listed on the posting) | Not stated | Oct 14, 2026 |
| Executive Director, Regulatory Affairs | 3 locations (listed on the posting) | Not stated | Oct 12, 2026 |
| Senior Investor Relations Manager | Boston, Massachusetts | Not stated | Oct 9, 2026 |
| Director, Analytical Development - Small Molecule | Waltham, Massachusetts | Not stated | Oct 9, 2026 |
Timeline
- Board tracked Radar started tracking this company’s job board (20 open jobs at last check). source ↗
- Partnership Partnership / licensing announced Feb 24, 2026. Source: company release on GlobeNewswire. source ↗
- Trial start Phase 3: A 26-Wk Study to Assess Safety & Efficacy of Tenapanor for T/t of Chronic Idiopathic Constipation in Adults source ↗
- Trial start Phase 2: 4-Week, Multi-center Dose-Ranging Study for the IBS-C in Pts. 6 to <12 Yrs source ↗
- Trial start Phase 1: An Open-label Study to Evaluate the Pharmacokinetics of Oral Tenapanor in Breast Milk of Lactating Females source ↗
- Trial start Phase 3: Safety Study of Tenapanor for the Treatment of Pediatric Patients (6 to Less Than 18 Years Old) With IBS-C source ↗
- Trial start Phase 3: Study to Assess Safety and Efficacy of Tenapanor for Treatment of IBS-C in Pediatric Patients 12 to Less Than 18 Years source ↗
- Trial start Phase 2: A Study Evaluating the Safety and Efficacy of RDX013 for the Treatment of Hyperkalemia source ↗
- Trial start Phase 4: Study to Evaluate the Use of Tenapanor as Core Therapy in the Treatment of Hyperphosphatemia source ↗
- Trial start Phase 4: A Long-Term Study of Tenapanor Alone or in Combination With Sevelamer in Patients With CKD on Dialysis and HP source ↗
- Trial start Phase 2/Phase 3: Study to Evaluate the Efficacy of Tenapanor as Adjunctive Therapy to Phosphate Binder Therapy source ↗
- Trial start 3: A Phase 3 Study of Tenapanor to Treat Hyperphosphatemia in ESRD Patients on Dialysis source ↗
- Trial start Phase 2: A Study Evaluating the Onset-of-Action, Safety, and Efficacy of RDX227675 for the Treatment of Hyperkalemia source ↗
- Trial start Phase 3: A Long-Term Safety Study of Tenapanor for the Treatment of IBS-C source ↗
- Trial start Phase 3: An 8-Week Study to Evaluate Tenapanor in the Treatment of Hyperphosphatemia in End-Stage Renal Disease Patients on Hemodialysis (ESRD-HD) source ↗
- Trial start Phase 3: A 26-Week Study to Evaluate the Efficacy and Safety of Tenapanor in IBS-C source ↗
- Trial start Phase 3: A 12-Week Study With a 4-Week Randomized Withdrawal Period to Evaluate the Efficacy and Safety of Tenapanor for the Treatment of IBS-C source ↗
- Trial start Phase 1: To Evaluate the Effect of AZD1722 on the Pharmacokinetics of Oral Midazolam in Healthy Volunteers source ↗
- Trial start Phase 1: To Assess the Effect of AZD1722 on the Pharmacokinetics of Cefadroxil in Healthy Volunteers source ↗
- Trial start Phase 1: AZD1722 Open Label, Absorption Distribution Metabolism and Excretion Study source ↗
- Trial start Phase 2: Dose Finding Study to Treat High Phosphate Levels in the Blood. source ↗
- Trial start Phase 2/Phase 3: The Efficacy of AZD1722 in Constipation Predominant Irritable Bowel Syndrome (IBS-C) source ↗
- Trial start Phase 1: Safety, Tolerability, Pharmacokinetics and Pharmacodynamic of AZD1722 in Healthy Male and Female Japanese Subjects source ↗
- Trial start Phase 2: A Study in CKD Patients With Type 2 Diabetes Mellitus and Albuminuria source ↗
- Trial start 1: A Phase 1 Study to Examine the Effect of Renvela on the Pharmacodynamics of AZD1722 source ↗
Upcoming milestones
- Feb 26, 2027 (ESTIMATED) · Phase 3 · A 26-Wk Study to Assess Safety & Efficacy of Tenapanor for T/t of Chronic Idiopathic Constipation in Adults · NCT07382167
- 2031-07 (ESTIMATED) · Phase 3 · Safety Study of Tenapanor for the Treatment of Pediatric Patients (6 to Less Than 18 Years Old) With IBS-C · NCT05905926
Open jobs 20
| Title | Location (from posting, not HQ) | Employer posted | First seen | Level |
|---|---|---|---|---|
| Area Business Director (Gastroenterology) - Los Angeles, CA | Los Angeles, California | Not stated | Oct 23, 2026 | Not stated |
| Associate Director, Market Access Training | 2 locations (listed on the posting) | Not stated | Oct 14, 2026 | Senior |
| Executive Director, Regulatory Affairs | 3 locations (listed on the posting) | Not stated | Oct 12, 2026 | Executive |
| Senior Investor Relations Manager | Boston, Massachusetts | Not stated | Oct 9, 2026 | Senior |
| Director, Analytical Development - Small Molecule | Waltham, Massachusetts | Not stated | Oct 9, 2026 | Senior |
| Logistics & Inventory Manager - Pharmaceutical | Newark, California | Not stated | Oct 9, 2026 | Mid |
| Field Reimbursement Manager - Chicago, IL | Chicago, Illinois | Not stated | Oct 9, 2026 | Mid |
| Field Reimbursement Manager - Houston, TX | Houston, Texas | Not stated | Oct 9, 2026 | Not stated |
| Field Reimbursement Manager - Monroe, LA | Monroe, Louisiana | Not stated | Oct 9, 2026 | Mid |
| Field Reimbursement Manager - Philadelphia | Philadelphia, Pennsylvania | Not stated | Oct 9, 2026 | Mid |
| Senior Medical Science Liaison (Gastroenterology) - Texas | 4 locations (listed on the posting) | Not stated | Oct 9, 2026 | Senior |
| Associate Director, Quality Auditing & Compliance | 2 locations (listed on the posting) | Not stated | Oct 9, 2026 | Senior |
| Executive Director, QMS & Digital - Onsite | Waltham, Massachusetts | Not stated | Oct 9, 2026 | Executive |
| Senior Quality Operations Manager | 2 locations (listed on the posting) | Not stated | Oct 9, 2026 | Senior |
| Senior Quality Training Specialist | Waltham, Massachusetts | Not stated | Oct 9, 2026 | Senior |
| Area Business Director (Gastroenterology) - Baltimore, MD | 3 locations (listed on the posting) | Not stated | Oct 9, 2026 | Senior |
| Area Business Director (Gastroenterology) - Fresno, CA | Fresno, California | Not stated | Oct 9, 2026 | Senior |
| Area Business Director (Gastroenterology) - Huntington Beach, CA | Huntington Beach, California | Not stated | Oct 9, 2026 | Senior |
| Area Business Director (Gastroenterology) - Long Beach, CA | Long Beach, California | Not stated | Oct 9, 2026 | Senior |
| Area Business Director (Gastroenterology) - Pasadena, CA | Pasadena, California | Not stated | Oct 9, 2026 | Senior |
Funding
- Partnership / licensing announced Feb 24, 2026. Source: company release on GlobeNewswire. source ↗
Clinical trials (lead sponsor) 29
| Record | Title | Phase | Status | Start | Primary completion |
|---|---|---|---|---|---|
| NCT05643534 | Study to Assess Safety and Efficacy of Tenapanor for Treatment of IBS-C in Pediatric Patients 12 to Less Than 18 Years | Phase 3 | Completed | Nov 15, 2022 | Aug 20, 2026 (actual) |
| NCT06553547 | 4-Week, Multi-center Dose-Ranging Study for the IBS-C in Pts. 6 to <12 Yrs | Phase 2 | Completed | Jul 24, 2024 | Jul 7, 2026 (actual) |
| NCT07382167 | A 26-Wk Study to Assess Safety & Efficacy of Tenapanor for T/t of Chronic Idiopathic Constipation in Adults | Phase 3 | Recruiting | Jan 13, 2026 | Feb 26, 2027 (estimated) |
| NCT05905926 | Safety Study of Tenapanor for the Treatment of Pediatric Patients (6 to Less Than 18 Years Old) With IBS-C | Phase 3 | Enrolling by invitation | Feb 17, 2023 | 2031-07 (estimated) |
| NCT06203444 | An Open-label Study to Evaluate the Pharmacokinetics of Oral Tenapanor in Breast Milk of Lactating Females | Phase 1 | Completed | Nov 27, 2023 | May 30, 2024 (actual) |
| NCT03427125 | A Phase 3 Study of Tenapanor to Treat Hyperphosphatemia in ESRD Patients on Dialysis | 3 | Completed | Jan 8, 2018 | Nov 15, 2019 (actual) |
| NCT04549597 | Study to Evaluate the Use of Tenapanor as Core Therapy in the Treatment of Hyperphosphatemia | Phase 4 | Completed | Nov 20, 2020 | Oct 13, 2021 (actual) |
| NCT03988920 | A Long-Term Study of Tenapanor Alone or in Combination With Sevelamer in Patients With CKD on Dialysis and HP | Phase 4 | Completed | Jun 15, 2019 | Jun 26, 2021 (actual) |
| NCT03824587 | Study to Evaluate the Efficacy of Tenapanor as Adjunctive Therapy to Phosphate Binder Therapy | Phase 2/Phase 3 | Completed | Feb 28, 2019 | Jul 17, 2019 (actual) |
| NCT04780841 | A Study Evaluating the Safety and Efficacy of RDX013 for the Treatment of Hyperkalemia | Phase 2 | Completed | Jan 11, 2021 | Dec 28, 2021 (actual) |
| NCT02081534 | Dose Finding Study to Treat High Phosphate Levels in the Blood. | Phase 2 | Completed | 2014-03 | 2014-11 (actual) |
| NCT02727751 | A Long-Term Safety Study of Tenapanor for the Treatment of IBS-C | Phase 3 | Completed | 2016-03 | 2017-10 (actual) |
| NCT01764854 | Pharmacodynamic Study of AZD1722 in End-stage Renal Disease Patients on Hemodialysis | Phase 2 | Completed | 2013-01 | 2013-10 (actual) |
| NCT02675998 | An 8-Week Study to Evaluate Tenapanor in the Treatment of Hyperphosphatemia in End-Stage Renal Disease Patients on Hemodialysis (ESRD-HD) | Phase 3 | Completed | 2016-01 | 2016-12 (actual) |
| NCT01847092 | A Study in CKD Patients With Type 2 Diabetes Mellitus and Albuminuria | Phase 2 | Completed | 2013-05 | 2015-03 (actual) |
| NCT02686138 | A 26-Week Study to Evaluate the Efficacy and Safety of Tenapanor in IBS-C | Phase 3 | Completed | 2015-12 | 2017-08 (actual) |
| NCT02621892 | A 12-Week Study With a 4-Week Randomized Withdrawal Period to Evaluate the Efficacy and Safety of Tenapanor for the Treatment of IBS-C | Phase 3 | Completed | 2015-10 | 2017-03 (actual) |
| NCT01923428 | The Efficacy of AZD1722 in Constipation Predominant Irritable Bowel Syndrome (IBS-C) | Phase 2/Phase 3 | Completed | 2013-08 | 2014-10 (actual) |
| NCT03018067 | A Study Evaluating the Onset-of-Action, Safety, and Efficacy of RDX227675 for the Treatment of Hyperkalemia | Phase 2 | Terminated | 2017-01 | 2017-05 (actual) |
| NCT01340053 | A Study to Evaluate the Safety and Efficacy of RDX5791 for the Treatment of Constipation Predominant Irritable Bowel Syndrome (IBS-C) | Phase 2 | Completed | 2011-05 | 2011-12 (actual) |
| NCT02819687 | Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of RDX5791 in Healthy Volunteers | Phase 1 | Completed | 2010-11 | 2011-03 (actual) |
| NCT02796131 | Safety, Tolerability, and Pharmacodynamics of RDX5791 in Healthy Volunteers | Phase 1 | Completed | 2011-07 | 2011-10 (actual) |
| NCT02063386 | AZD1722 Open Label, Absorption Distribution Metabolism and Excretion Study | Phase 1 | Completed | 2014-04 | 2014-05 (actual) |
| NCT02226783 | D5611C00003 - Food Interaction Study With AZD1722 Tablet in Healthy Subjects | Phase 1 | Completed | 2013-03 | 2013-10 (actual) |
| NCT02140268 | To Evaluate the Effect of AZD1722 on the Pharmacokinetics of Oral Midazolam in Healthy Volunteers | Phase 1 | Completed | 2014-05 | 2014-08 (actual) |
| NCT02140281 | To Assess the Effect of AZD1722 on the Pharmacokinetics of Cefadroxil in Healthy Volunteers | Phase 1 | Completed | 2014-05 | 2014-08 (actual) |
| NCT02346890 | A Phase 1 Study to Examine the Effect of Renvela on the Pharmacodynamics of AZD1722 | 1 | Completed | 2013-04 | 2013-04 (actual) |
| NCT02249936 | A Phase 1 Study to Examine the Pharmacodynamics of Different AZD1722 Formulations | 1 | Completed | 2013-02 | 2013-02 (actual) |
| NCT02176252 | Safety, Tolerability, Pharmacokinetics and Pharmacodynamic of AZD1722 in Healthy Male and Female Japanese Subjects | Phase 1 | Completed | 2013-07 | 2013-12 (actual) |