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NCT02253654 · ClinicalTrials.gov registry record · Phase 4

Evaluation of Two Epoetin Alfa Dosing Strategies in Subjects With Chronic Kidney Disease Receiving Hemodialysis

A Phase 4 study, sponsored by Amgen.

Completed
Registry status
Phase 4
Development phase
216
Enrollment target

NCT02253654: Completed Phase 4 study, sponsored by Amgen.

NCT02253654 is a Phase 4 study that has completed, run by Amgen. The registered enrollment target is 216 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (58% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02253654, a Phase 4 study, has completed, sponsored by Amgen.

COMPLETED
Registry status
Phase 4
Development phase
216 participants
Enrollment target

Study Summary

The purpose of this study is to compare two different dosing methods of epoetin alfa and their effectiveness in maintaining hemoglobin levels between 10.0 to 11.0 g/dL in in patients with chronic kidney disease (CKD) receiving hemodialysis.

Primary Outcome

Hemoglobin was measured every 2 weeks during the evaluation period. The percentage of these measurements that were within the range of 10-11 g/dL was calculated for each participant.

Interventions

  • DRUG Epoetin alfa

Trial Details

FieldValue
Enrollment Target 216 participants
Start Date 2015-04-01
Est. Completion 2016-05-25
Phase Phase 4
Amgen

558 total trials

What the finished NCT02253654 record still lists

NCT02253654 is an interventional study that assigns participants to a tested intervention. The registered 216 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (58% lower).

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

NCT02253654 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02253654 about?

NCT02253654 is a clinical study titled "Evaluation of Two Epoetin Alfa Dosing Strategies in Subjects With Chronic Kidney Disease Receiving Hemodialysis". The purpose of this study is to compare two different dosing methods of epoetin alfa and their effectiveness in maintaining hemoglobin levels between 10.0 to 11.0 g/dL in in patients with chronic kidney disease (CKD) receiving hemodialysis.

What is the current status of trial NCT02253654?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 216 participants. The study started on 2015-04-01. Estimated completion is 2016-05-25.

What interventions are being tested in trial NCT02253654?

The interventions under investigation include: Epoetin alfa (DRUG).

Who is sponsoring clinical trial NCT02253654?

This trial is sponsored by Amgen, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02253654's enrollment target sits among peer trials

216 393rd of 2000 higher than 1,607 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT02253654, the US trial registry maintained by the National Library of Medicine. NCT02253654 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.