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NCT02268994 · ClinicalTrials.gov registry record · Phase 3

KRX-0502 (Ferric Citrate) for the Treatment of IDA in Adult Subjects With NDD-CKD

A Phase 3 study, sponsored by Keryx Biopharmaceuticals.

Completed
Registry status
Phase 3
Development phase
234
Enrollment target

NCT02268994: Completed Phase 3 study, sponsored by Keryx Biopharmaceuticals.

NCT02268994 is a Phase 3 study that has completed, run by Keryx Biopharmaceuticals. The registered enrollment target is 234 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02268994, a Phase 3 study, has completed, sponsored by Keryx Biopharmaceuticals.

COMPLETED
Registry status
Phase 3
Development phase
234 participants
Enrollment target

Study Summary

a 24-week phase 3, multi-center clinical trial, comprised of a 16-week, randomized, double-blind, placebo-controlled period ("Randomized Period"), followed by an 8-week open-label safety extension period, where all subjects receive KRX-0502 (ferric citrate) ("Extension Period").

Primary Outcome

Efficacy analyses were performed for the Intention-to-treat (ITT) population, the population consisted of all subjects who were randomized, had a baseline laboratory value, took at least 1 dose of study drug, and had at least 1 post-baseline laboratory assessment during the randomized period.

Interventions

  • DRUG Placebo
  • DRUG ferric citrate

Trial Details

FieldValue
Enrollment Target 234 participants
Start Date 2014-10
Est. Completion 2016-01
Phase Phase 3
Keryx Biopharmaceuticals

9 total trials

What the finished NCT02268994 record still lists

NCT02268994 is an interventional study that assigns participants to a tested intervention. The registered 234 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (70% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02268994 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02268994 about?

NCT02268994 is a clinical study titled "KRX-0502 (Ferric Citrate) for the Treatment of IDA in Adult Subjects With NDD-CKD". a 24-week phase 3, multi-center clinical trial, comprised of a 16-week, randomized, double-blind, placebo-controlled period ("Randomized Period"), followed by an 8-week open-label safety extension period, where all subjects receive KRX-0502 (ferric citrate) ("Extension Period").

What is the current status of trial NCT02268994?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 234 participants. The study started on 2014-10. Estimated completion is 2016-01.

What interventions are being tested in trial NCT02268994?

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

Who is sponsoring clinical trial NCT02268994?

This trial is sponsored by Keryx Biopharmaceuticals, which has 9 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02268994's enrollment target sits among peer trials

234 1297th of 2000 higher than 703 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT02268994, the US trial registry maintained by the National Library of Medicine. NCT02268994 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.