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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 Oct 25, 2026, 12:01 AM 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)

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
NCT03238911
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pharmacosmos A/S
Industry
Enrollment
123 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 24, 2017 (Actual)
Primary completion
Jun 19, 2018 (Actual)
Completion
Jun 19, 2018 (Actual)
Last update posted
Feb 25, 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 25, 2020 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03238911 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →