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Completed Phase 3 Interventional Results available

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

ClinicalTrials.gov ID: NCT03237065

Public ClinicalTrials.gov record NCT03237065. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 10:58 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Open-label, Comparative Trial Comparing the Incidence of Hypophosphatemia in Relation to Treatment With Iron Isomaltoside/Ferric Derisomaltose and Ferric Carboxymaltose in Subjects With Iron Deficiency Anaemia (Phosphare-IDA-05)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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).

Study identification

NCT ID
NCT03237065
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pharmacosmos A/S
Industry
Enrollment
122 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 30, 2017 (Actual)
Primary completion
May 29, 2018 (Actual)
Completion
May 29, 2018 (Actual)
Last update posted
Feb 25, 2020

2017 – 2018

United States locations

U.S. sites
15
U.S. states
9
U.S. cities
14
Facility City State ZIP Site status
Pharmacosmos Investigational Site Muscle Shoals Alabama 35661 —
Pharmacosmos Investigational Site Doral Florida 33122 —
Pharmacosmos Investigational Site Miami Florida 33144 —
Pharmacosmos Investigational Site Miami Florida 33165 —
Pharmacosmos Investigational Site Miami Lakes Florida 33014 —
Pharmacosmos Investigational Site Orlando Florida 32819 —
Pharmacosmos Investigational Site Idaho Falls Idaho 83404 —
Pharmacosmos Investigational Site Oak Brook Illinois 60523 —
Pharmacosmos investigational Site Flint Michigan 48504 —
Pharmacosmos Investigational Site St Louis Missouri 63119 —
Pharmacosmos Investigational Site Las Vegas Nevada 89146 —
Pharmacosmos Investigational Site Albuquerque New Mexico 87102 —
Pharmacosmos Investigational Site Morehead City North Carolina 28557 —
Pharmacosmos Investigational Site Raleigh North Carolina 27607 —
Pharmacosmos Investigational Site Winston-Salem North Carolina 27103 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03237065, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 25, 2020 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03237065 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →