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NCT01280240 · ClinicalTrials.gov registry record · Phase 1

Pharmacokinetic Study of Iron Isomaltoside 1000 Administered by 250 mg IV Bolus Injection or 500 mg Intravenous Infusion to Patients With Non-hematological Malignancies Associated With Chemotherapy Induced Anaemia

A Phase 1 study, sponsored by Pharmacosmos A/S.

Completed
Registry status
Phase 1
Development phase
11
Enrollment target

NCT01280240: Completed Phase 1 study, sponsored by Pharmacosmos A/S.

NCT01280240 is a Phase 1 study that has completed, run by Pharmacosmos A/S. The registered enrollment target is 11 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (82% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01280240, a Phase 1 study, has completed, sponsored by Pharmacosmos A/S.

COMPLETED
Registry status
Phase 1
Development phase
11 participants
Enrollment target

Study Summary

The purpose of this study is to assess Pharmakokinetic properties of iron isomaltoside 1000 (Monofer®) in doses of 250 mg and 500 mg in patients suffering from Chemotherapy Induced anemia.

Interventions

  • DRUG Monofer(R)

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2012-03
Est. Completion 2012-11
Phase Phase 1
Pharmacosmos A/S

10 total trials

What the finished NCT01280240 record still lists

NCT01280240 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 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (82% lower).

The record links to 0 conditions, and to 1 intervention - of which Monofer(R) is the first listed.

NCT01280240 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01280240 about?

NCT01280240 is a clinical study titled "Pharmacokinetic Study of Iron Isomaltoside 1000 Administered by 250 mg IV Bolus Injection or 500 mg Intravenous Infusion to Patients With Non-hematological Malignancies Associated With Chemotherapy Induced Anaemia". The purpose of this study is to assess Pharmakokinetic properties of iron isomaltoside 1000 (Monofer®) in doses of 250 mg and 500 mg in patients suffering from Chemotherapy Induced anemia.

What is the current status of trial NCT01280240?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 11 participants. The study started on 2012-03. Estimated completion is 2012-11.

What interventions are being tested in trial NCT01280240?

The interventions under investigation include: Monofer(R) (DRUG).

Who is sponsoring clinical trial NCT01280240?

This trial is sponsored by Pharmacosmos A/S, which has 10 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01280240's enrollment target sits among peer trials

11 1911th of 2000 higher than 88 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT01280240, the US trial registry maintained by the National Library of Medicine. NCT01280240 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.