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NCT03087058 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by Vifor Pharma.

Terminated
Registry status
Phase 2
Development phase
23
Enrollment target

NCT03087058: Clinical Trial Phase 2 study, sponsored by Vifor Pharma.

NCT03087058 is a Phase 2 study that was terminated before completion, run by Vifor Pharma. The registered enrollment target is 23 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (83% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03087058, a Phase 2 study, was terminated before completion, sponsored by Vifor Pharma.

TERMINATED
Registry status
Phase 2
Development phase
23 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the change in serum potassium levels from start of treatment to Day 14, when patiromer is administered at different doses, once daily, in children 2 - \< 18 years of age with chronic kidney disease (CKD) and hyperkalemia (too much potassium in the blood). Another purpose of the study is to evaluate the safety and tolerability of patiromer in children 2 - \< 18 years of age with CKD and hyperkalemia.

Interventions

  • DRUG Patiromer

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2017-07-07
Est. Completion 2021-04-30
Phase Phase 2
Vifor Pharma

12 total trials

Why NCT03087058 stopped before completion

NCT03087058 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 23 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (83% lower).

The record links to 0 conditions, and to 1 intervention - of which Patiromer is the first listed.

NCT03087058 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03087058 about?

NCT03087058 is a clinical study titled "Pharmacodynamic & Safety of Patiromer in Children & Adolescents (2-<18 Yrs) With Chronic Kidney Disease and Hyperkalemia". The purpose of this study is to evaluate the change in serum potassium levels from start of treatment to Day 14, when patiromer is administered at different doses, once daily, in children 2 - \< 18 years of age with chronic kidney disease (CKD) and hyperkalemia (too much potassium in the blood). Ano...

What is the current status of trial NCT03087058?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 23 participants. The study started on 2017-07-07. Estimated completion is 2021-04-30.

What interventions are being tested in trial NCT03087058?

The interventions under investigation include: Patiromer (DRUG).

Who is sponsoring clinical trial NCT03087058?

This trial is sponsored by Vifor Pharma, which has 12 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03087058's enrollment target sits among peer trials

23 1784th of 2000 higher than 211 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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

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Source: ClinicalTrials.gov NCT03087058, the US trial registry maintained by the National Library of Medicine. NCT03087058 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.