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Completed Phase 3 Interventional Results available

Open-label Safety and Efficacy of Sodium Zirconium Cyclosilicate for up to 12 Months

ClinicalTrials.gov ID: NCT02163499

Public ClinicalTrials.gov record NCT02163499. 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 21, 2026, 10:16 PM EDT

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

Official title

Multicenter, Multi-Dose, Open-Label Maintenance of Long-Term Safety and Efficacy of Sodium Zirconium Cyclosilicate (ZS) in Hyperkalemia

Study identification

NCT ID
NCT02163499
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
ZS Pharma, Inc.
Industry
Enrollment
751 participants

Conditions and interventions

Conditions

Interventions

  • Sodium Zirconium Cyclosilicate 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
Jun 29, 2014
Primary completion
Nov 29, 2016
Completion
Nov 29, 2016
Last update posted
Jun 26, 2018

2014 – 2016

United States locations

U.S. sites
36
U.S. states
17
U.S. cities
34
Facility City State ZIP Site status
Not listed Scottsboro Alabama 35768
Not listed Tempe Arizona 85284
Not listed Tucson Arizona 85724
Not listed Chula Vista California 90717
Not listed Los Angeles California 90022
Not listed Paramount California 90723
Not listed Riverside California 92505
Not listed Sacramento California 95825
Not listed Whittier California 90603
Not listed Denver Colorado 80230
Not listed Brandon Florida 33511
Not listed DeLand Florida 32720
Not listed Hudson Florida 34667
Not listed Lauderdale Lakes Florida 33313
Not listed Miami Florida 33015
Not listed Miami Florida 33125
Not listed Miami Lakes Florida 33018
Not listed New Smyrna Beach Florida 32168
Not listed Tampa Florida 33614
Not listed Winter Park Florida 32789
Not listed Columbus Georgia 31901
Not listed Evergreen Park Illinois 60805
Not listed Joliet Illinois 60435
Not listed Paducah Kentucky 42003
Not listed Shreveport Louisiana 71101
Not listed Chesterfield Michigan 48047
Not listed Kansas City Missouri 64411
Not listed St Louis Missouri 63110
Not listed Great Neck New York 11021
Not listed Providence Rhode Island 02903
Not listed Orangeburg South Carolina 29118
Not listed Sumter South Carolina 29150
Not listed Chattanooga Tennessee 37408
Not listed San Antonio Texas 78215
Not listed San Antonio Texas 78229
Not listed St. George Utah 84770

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 14 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02163499, 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 Jun 26, 2018 · Synced Jul 21, 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 NCT02163499 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →