Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00598273 · ClinicalTrials.gov registry record · Phase 3

Safety & Efficacy of Peginesatide for the Treatment of Anemia in Participants With Chronic Renal Failure Not on Dialysis

A Phase 3 study, sponsored by Affymax.

Completed
Registry status
Phase 3
Development phase
490
Enrollment target

NCT00598273: Completed Phase 3 study, sponsored by Affymax.

NCT00598273 is a Phase 3 study that has completed, run by Affymax. The registered enrollment target is 490 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (37% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00598273, a Phase 3 study, has completed, sponsored by Affymax.

COMPLETED
Registry status
Phase 3
Development phase
490 participants
Enrollment target

Study Summary

The purpose of this study was to evaluate the safety and efficacy of peginesatide for the treatment of anemia in participants with chronic kidney disease, who are not on dialysis and not on erythropoiesis stimulating agent (ESA) treatment.

Primary Outcome

The baseline hemoglobin value is defined as the mean of three hemoglobin values: the two most recent hemoglobin values taken prior to the day of randomization and the value obtained on the day of randomization. The mean hemoglobin during the Evaluation Period for each participant is calculated as the mean of the available hemoglobin values during Study Weeks 25 through 36.

Interventions

  • DRUG Darbepoetin alfa
  • DRUG peginesatide

Trial Details

FieldValue
Enrollment Target 490 participants
Start Date 2007-10
Est. Completion 2010-02
Phase Phase 3
Affymax

6 total trials

What the finished NCT00598273 record still lists

NCT00598273 is an interventional study that assigns participants to a tested intervention. The registered 490 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 (37% lower).

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

NCT00598273 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00598273 about?

NCT00598273 is a clinical study titled "Safety & Efficacy of Peginesatide for the Treatment of Anemia in Participants With Chronic Renal Failure Not on Dialysis". The purpose of this study was to evaluate the safety and efficacy of peginesatide for the treatment of anemia in participants with chronic kidney disease, who are not on dialysis and not on erythropoiesis stimulating agent (ESA) treatment.

What is the current status of trial NCT00598273?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 490 participants. The study started on 2007-10. Estimated completion is 2010-02.

What interventions are being tested in trial NCT00598273?

The interventions under investigation include: Darbepoetin alfa (DRUG), peginesatide (DRUG).

Who is sponsoring clinical trial NCT00598273?

This trial is sponsored by Affymax, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00598273's enrollment target sits among peer trials

490 782nd of 2000 higher than 1,218 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT04728893 · 490 participants · Phase 2

    Efficacy and Safety of Nemtabrutinib (MK-1026) in Participants With Hematologic Malignancies (MK-1026-003)

  • NCT06238479 · 490 participants · Phase 1

    A Study of LY4101174 in Participants With Recurrent, Advanced or Metastatic Solid Tumors

  • NCT06336928 · 490 participants

    A Validation Study to Determine Concordance of Liquid Biopsy and Breast Cancer Diagnosis

  • NCT06641414 · 490 participants · Phase 3

    Lisaftoclax (APG-2575) Combined With Azacytidine (AZA) in the Treatment of Patients With Higher-risk Myelodysplastic Syndrome (GLORA-4).

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00598273, the US trial registry maintained by the National Library of Medicine. NCT00598273 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.