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NCT03237065 · ClinicalTrials.gov registry record · Phase 3

Incidence of Hypophosphatemia After Treatment With Iron Isomaltoside/Ferric Derisomaltose or Ferric Carboxymaltose in Subjects With Iron Deficiency Anaemia

A Phase 3 study, sponsored by Pharmacosmos A/S.

Completed
Registry status
Phase 3
Development phase
122
Enrollment target

NCT03237065: Completed Phase 3 study, sponsored by Pharmacosmos A/S.

NCT03237065 is a Phase 3 study that has completed, run by Pharmacosmos A/S. The registered enrollment target is 122 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (84% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03237065, a Phase 3 study, has completed, sponsored by Pharmacosmos A/S.

COMPLETED
Registry status
Phase 3
Development phase
122 participants
Enrollment target

Study Summary

The trial was designed to evaluate the incidence of unintended hypophosphatemia (low level of phosphate in the blood) in subjects with iron deficiency anaemia (IDA).

Primary Outcome

Safety The incidence of hypophosphatemia (defined as s-phosphate \<2 mg/dL) at any time from baseline up to day 35.

Interventions

  • DRUG Ferric carboxymaltose
  • DRUG Iron isomaltoside/ferric derisomaltose

Trial Details

FieldValue
Enrollment Target 122 participants
Start Date 2017-10-30
Est. Completion 2018-05-29
Phase Phase 3
Pharmacosmos A/S

10 total trials

What the finished NCT03237065 record still lists

NCT03237065 is an interventional study that assigns participants to a tested intervention. The registered 122 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 (84% lower).

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

NCT03237065 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03237065 about?

NCT03237065 is a clinical study titled "Incidence of Hypophosphatemia After Treatment With Iron Isomaltoside/Ferric Derisomaltose or Ferric Carboxymaltose in Subjects With Iron Deficiency Anaemia". The trial was designed to evaluate the incidence of unintended hypophosphatemia (low level of phosphate in the blood) in subjects with iron deficiency anaemia (IDA).

What is the current status of trial NCT03237065?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 122 participants. The study started on 2017-10-30. Estimated completion is 2018-05-29.

What interventions are being tested in trial NCT03237065?

The interventions under investigation include: Ferric carboxymaltose (DRUG), Iron isomaltoside/ferric derisomaltose (DRUG).

Who is sponsoring clinical trial NCT03237065?

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 NCT03237065's enrollment target sits among peer trials

122 1617th of 2000 higher than 382 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 NCT03237065, the US trial registry maintained by the National Library of Medicine. NCT03237065 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.