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Completed Phase 4 Interventional Results available

Patiromer With or Without Food for the Treatment of Hyperkalemia

ClinicalTrials.gov ID: NCT02694744

Public ClinicalTrials.gov record NCT02694744. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 1:47 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

The Effect of Food: An Open-Label, Randomized, Parallel Group Phase 4 Study of the Efficacy and Safety of Patiromer for Oral Suspension With or Without Food for the Treatment of Hyperkalemia (TOURMALINE)

Study identification

NCT ID
NCT02694744
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Relypsa, Inc.
Industry
Enrollment
114 participants

Conditions and interventions

Conditions

Interventions

  • patiromer Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 31, 2016
Primary completion
Jun 30, 2016
Completion
Jul 31, 2016
Last update posted
May 11, 2021

2016

United States locations

U.S. sites
29
U.S. states
13
U.S. cities
24
Facility City State ZIP Site status
Investigator Site 12 Fountain Valley California 92708
Investigator Site 11 Huntington Beach California 92648
Investigator Site 38 Palm Springs California 92262
Investigator Site 20 Riverside California 92505
Investigator Site 21 San Dimas California 91773
Investigator Site 24 Denver Colorado 80230
Investigator Site 30 Edgewater Florida 32132
Investigator Site 10 Hialeah Florida 33012
Investigator Site 13 Hollywood Florida 33021
Investigator Site 17 Lauderdale Lakes Florida 33313-1638
Investigator Site 16 Lauderdale Lakes Florida 33319
Investigator Site 15 Miami Florida 33015
Investigator Site 43 Miami Florida 33147
Investigator Site 18 Pembroke Pines Florida 33028
Investigator Site 27 Tampa Florida 33614
Investigator Site 44 Meridian Idaho 83642
Investigator Site 39 Aurora Illinois 60504
Investigator Site 23 Flint Michigan 48504
Investigator Site 34 Kansas City Missouri 64111
Investigator Site 41 Las Vegas Nevada 89106
Investigator Site 37 Flushing New York 11355
Investigator Site 36 Norman Oklahoma 73069
Investigator Site 40 Jackson Tennessee 38305
Investigator Site 33 Dallas Texas 75231
Investigator Site 26 San Antonio Texas 78202
Investigator Site 29 San Antonio Texas 78207
Investigator Site 28 San Antonio Texas 78215
Investigator Site 25 San Antonio Texas 78229
Investigator Site 22 Salt Lake City Utah 84124

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02694744, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 11, 2021 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02694744 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →