Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02694744 · ClinicalTrials.gov registry record · Phase 4
Patiromer With or Without Food for the Treatment of Hyperkalemia
A Phase 4 study, sponsored by Relypsa.
- Completed
- Registry status
- Phase 4
- Development phase
- 114
- Enrollment target
NCT02694744: Completed Phase 4 study, sponsored by Relypsa.
NCT02694744 is a Phase 4 study that has completed, run by Relypsa. The registered enrollment target is 114 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (78% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02694744, a Phase 4 study, has completed, sponsored by Relypsa.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 114 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the efficacy and safety of patiromer administered once daily (QD) when given with food compared to without food (experimental treatment group) for the treatment of hyperkalemia (high potassium in the blood).
Interventions
- DRUG patiromer
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 114 participants |
| Start Date | 2016-02 |
| Est. Completion | 2016-08 |
| Phase | Phase 4 |
What the finished NCT02694744 record still lists
NCT02694744 is an interventional study that assigns participants to a tested intervention. The registered 114 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (78% lower).
The record links to 0 conditions, and to 1 intervention - of which patiromer is the first listed.
NCT02694744 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02694744 about?
NCT02694744 is a clinical study titled "Patiromer With or Without Food for the Treatment of Hyperkalemia". The purpose of this study is to evaluate the efficacy and safety of patiromer administered once daily (QD) when given with food compared to without food (experimental treatment group) for the treatment of hyperkalemia (high potassium in the blood).
What is the current status of trial NCT02694744?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 114 participants. The study started on 2016-02. Estimated completion is 2016-08.
What interventions are being tested in trial NCT02694744?
The interventions under investigation include: patiromer (DRUG).
Who is sponsoring clinical trial NCT02694744?
This trial is sponsored by Relypsa, which has 5 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02694744's enrollment target sits among peer trials
114 720th of 2000 higher than 1,278 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT04522791 · 114 participants · Phase 2
Breathing, Relaxation, Attention Training, & Health in Older Adults (BREATHE)
- NCT04875052 · 114 participants · NA
Vibration and Post-traumatic Osteoarthritis Risk Following ACL Injury
- NCT05100342 · 114 participants
Prospective Validation of a Points Score System Predicting 30-day Survival
- NCT05224089 · 114 participants · Phase 4
Bilateral TAP and RS Blocks Using Liposomal Bupivacaine/Bupivacaine vs. Regular Bupivacaine in Laparoscopic Colectomy
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia