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NCT04780841 · ClinicalTrials.gov registry record · Phase 2

A Study Evaluating the Safety and Efficacy of RDX013 for the Treatment of Hyperkalemia

A Phase 2 study of Hyperkalemia, sponsored by Ardelyx.

Completed
Registry status
Phase 2
Development phase
109
Enrollment target
6
Study locations

NCT04780841 is a Phase 2 study of Hyperkalemia that has completed, run by Ardelyx. The registered enrollment target is 109 participants, above the 48-participant average among 8 other Hyperkalemia trials with a reported enrollment target (127% higher). The trial reports 6 study locations across 4 states.

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The verdict

NCT04780841, a Phase 2 study of Hyperkalemia, has completed, sponsored by Ardelyx.

COMPLETED
Registry status
Phase 2
Development phase
109 participants
Enrollment target
6
Study locations

Study Summary

The purpose of this study is to evaluate the ability of RDX013 to lower serum potassium in patients with chronic kidney disease with elevated serum potassium levels

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG RDX013

Study Locations (6)

Florida

  • Horizon Research Group LLC - Coral Gables
  • Panax Clinical Research LLC - Miami Lakes
  • South Florida Research Phase I-IV; Inc. - Miami Springs

Louisiana

  • NW Louisiana Nephrology Assoc - Shreveport

Missouri

  • Clinical Research Consultants - Kansas City

North Carolina

  • Mountain Kidney & Hypertension Associates - Asheville

Trial Details

FieldValue
Enrollment Target 109 participants
Start Date 2021-01-11
Est. Completion 2022-03-03
Phase Phase 2

Sponsor

Ardelyx

25 total trials

What the Registry Record Tells You About NCT04780841

The ClinicalTrials.gov registry entry for NCT04780841 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 109 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 48-participant average among 8 other Hyperkalemia trials with a reported enrollment target (127% higher). The listed sponsor is Ardelyx, which has 25 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Hyperkalemia appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT04780841 reports 6 study locations spanning 4 distinct geographic areas - top geographies include Florida, Louisiana, Missouri.

Frequently Asked Questions

What is clinical trial NCT04780841 about?

NCT04780841 is a clinical study titled "A Study Evaluating the Safety and Efficacy of RDX013 for the Treatment of Hyperkalemia". The purpose of this study is to evaluate the ability of RDX013 to lower serum potassium in patients with chronic kidney disease with elevated serum potassium levels

What is the current status of trial NCT04780841?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 109 participants. The study started on 2021-01-11. Estimated completion is 2022-03-03.

What conditions does trial NCT04780841 study?

This clinical trial studies the following conditions: Hyperkalemia.

What interventions are being tested in trial NCT04780841?

The interventions under investigation include: Placebo (DRUG), RDX013 (DRUG).

Who is sponsoring clinical trial NCT04780841?

This trial is sponsored by Ardelyx, which has 25 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04780841 being conducted?

This trial has 6 study locations across Florida, Louisiana, Missouri, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Hyperkalemia

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.