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NCT00721188 · ClinicalTrials.gov registry record · Phase 2

Iron Sucrose in Non-Dialysis Dependent (NDD-CKD) Pediatric Patients

A Phase 2 study of Anemia, sponsored by American Regent.

Completed
Registry status
Phase 2
Development phase
11
Enrollment target
1
Study location

NCT00721188: Completed Phase 2 study of Anemia, sponsored by American Regent.

NCT00721188 is a Phase 2 study of Anemia that has completed, run by American Regent. The registered enrollment target is 11 participants, below the 427-participant average among 72 other Anemia trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00721188, a Phase 2 study of Anemia, has completed, sponsored by American Regent.

COMPLETED
Registry status
Phase 2
Development phase
11 participants
Enrollment target
1
Study location

Study Summary

The primary objective of this study is to assess the pharmacokinetics of Venofer (Iron Sucrose Injection) in NDD-CKD pediatric patients.

Conditions Studied

Interventions

  • DRUG Venofer

Study Locations (1)

Pennsylvania

  • Luitpold Pharmaceuticals - Norristown

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2006-01
Est. Completion 2010-01
Phase Phase 2
American Regent

34 total trials

What the finished NCT00721188 record still lists

NCT00721188 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 11 participants, a relatively small participant target, below the 427-participant average among 72 other Anemia trials with a reported enrollment target (97% lower).

The record links to 1 condition, with Anemia appearing as the primary indexed condition, and to 1 intervention - of which Venofer is the first listed.

NCT00721188 reports a single indexed study location in Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT00721188 about?

NCT00721188 is a clinical study titled "Iron Sucrose in Non-Dialysis Dependent (NDD-CKD) Pediatric Patients". The primary objective of this study is to assess the pharmacokinetics of Venofer (Iron Sucrose Injection) in NDD-CKD pediatric patients.

What is the current status of trial NCT00721188?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 11 participants. The study started on 2006-01. Estimated completion is 2010-01.

What conditions does trial NCT00721188 study?

This clinical trial studies the following conditions: Anemia.

What interventions are being tested in trial NCT00721188?

The interventions under investigation include: Venofer (DRUG).

Who is sponsoring clinical trial NCT00721188?

This trial is sponsored by American Regent, which has 34 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00721188 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Anemia

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00721188's enrollment target sits among peer trials

11 70th of 72 higher than 3 of 72 other Anemia trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Anemia 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 NCT00721188, the US trial registry maintained by the National Library of Medicine. NCT00721188 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.