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Terminated Phase 2 Interventional Results available

Pharmacodynamic & Safety of Patiromer in Children & Adolescents (2-<18 Yrs) With Chronic Kidney Disease and Hyperkalemia

ClinicalTrials.gov ID: NCT03087058

Public ClinicalTrials.gov record NCT03087058. 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, 2:24 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

A Phase 2, Open-Label, Multiple Dose Study to Evaluate the Pharmacodynamic Effects, Safety, and Tolerability of Patiromer for Oral Suspension in Children and Adolescents 2 to < 18 Years of Age With Chronic Kidney Disease and Hyperkalemia

Study identification

NCT ID
NCT03087058
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Vifor Pharma, Inc.
Industry
Enrollment
23 participants

Conditions and interventions

Conditions

Interventions

  • Patiromer Drug

Drug

Eligibility (public fields only)

Age range
2 Years to 17 Years
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
Jul 6, 2017
Primary completion
Jan 12, 2021
Completion
Apr 29, 2021
Last update posted
Oct 18, 2022

2017 – 2021

United States locations

U.S. sites
10
U.S. states
8
U.S. cities
10
Facility City State ZIP Site status
Investigator Site 1107 Palo Alto California 94394
Investigator Site 1101 Kansas City Kansas 64108
Investigator Site 1103 Baltimore Maryland 21287
Investigator Site 1102 The Bronx New York 10467
Investigator Site 1105 Cincinnati Ohio 45229
Investigator Site 1108 Pittsburgh Pennsylvania 15224
Investigator Site 1104 Amarillo Texas 79106
Investigator Site 1109 Dallas Texas 75235
Investigator Site 1113 Houston Texas 77030
Investigator Site 1106 Madison Wisconsin 53792

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 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03087058, 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 Oct 18, 2022 · 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 NCT03087058 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →