Patiromer With or Without Food for the Treatment of Hyperkalemia

Completed · Phase 4

Conditions studied: Hyperkalemia

In brief

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).

Key facts

Study ID

NCT02694744

Run by

Relypsa, Inc.

People needed

114

Starts

2016-02-01

Expected to finish

2016-08-01

Last updated by the study team

2021-05-12

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

• Investigator Site 12 — Fountain Valley, California, United States
• Investigator Site 11 — Huntington Beach, California, United States
• Investigator Site 38 — Palm Springs, California, United States
• Investigator Site 20 — Riverside, California, United States
• Investigator Site 21 — San Dimas, California, United States
• Investigator Site 24 — Denver, Colorado, United States
• Investigator Site 30 — Edgewater, Florida, United States
• Investigator Site 10 — Hialeah, Florida, United States
• Investigator Site 13 — Hollywood, Florida, United States
• Investigator Site 17 — Lauderdale Lakes, Florida, United States
• Investigator Site 16 — Lauderdale Lakes, Florida, United States
• Investigator Site 15 — Miami, Florida, United States
• Investigator Site 43 — Miami, Florida, United States
• Investigator Site 18 — Pembroke Pines, Florida, United States
• Investigator Site 27 — Tampa, Florida, United States
• Investigator Site 44 — Meridian, Idaho, United States
• Investigator Site 39 — Aurora, Illinois, United States
• Investigator Site 23 — Flint, Michigan, United States
• Investigator Site 34 — Kansas City, Missouri, United States
• Investigator Site 41 — Las Vegas, Nevada, United States
• Investigator Site 37 — Flushing, New York, United States
• Investigator Site 36 — Norman, Oklahoma, United States
• Investigator Site 40 — Jackson, Tennessee, United States
• Investigator Site 33 — Dallas, Texas, United States
• Investigator Site 26 — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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