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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 Jul 21, 2026, 4:42 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)

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

Interventions

  • Iron isomaltoside/ferric derisomaltose Drug
  • Ferric carboxymaltose Drug

Drug

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 29, 2017
Primary completion
May 28, 2018
Completion
May 28, 2018
Last update posted
Feb 24, 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 24, 2020 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03237065 live on ClinicalTrials.gov.

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