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Completed Phase 3 Interventional Results available

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

ClinicalTrials.gov ID: NCT03238911

Public ClinicalTrials.gov record NCT03238911. 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, 10:50 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-04)

Study identification

NCT ID
NCT03238911
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pharmacosmos A/S
Industry
Enrollment
123 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 23, 2017
Primary completion
Jun 18, 2018
Completion
Jun 18, 2018
Last update posted
Feb 24, 2020

2017 – 2018

United States locations

U.S. sites
16
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
Pharmacosmos Investigational Site Los Angeles California 90036
Pharmacosmos Investigational Site Sacramento California 95831
Pharmacosmos Investigational Site Santa Ana California 92704
Pharmacosmos Investigational Site Clearwater Florida 33759
Pharmacosmos Investigational Site Miami Florida 33125
Pharmacosmos Investigational Site 1 Miami Florida 33126
Pharmacosmos Investigational Site 2 Miami Florida 33126
Pharmacosmos Investigational Site Miami Florida 33143
Pharmacosmos Investigational Site Miami Florida 33144
Pharmacosmos Investigational Site Indianapolis Indiana 46202
Pharmacosmos Investigational Site Wichita Kansas 67206
Pharmacosmos Investigational Site Metairie Louisiana 70001
Pharmacosmos Investigational Site Lancaster Pennsylvania 17605
Pharmacosmos Investigational Site Houston Texas 77024
Pharmacosmos Investigational Site Orem Utah 84058
Pharmacosmos Investigational Site Leesburg Virginia 20176

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 NCT03238911, 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 NCT03238911 live on ClinicalTrials.gov.

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