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Completed Phase 3 Interventional Results available

An Extension Trial to Assess the Safety of Re-dosing of Iron Isomaltoside/Ferric Derisomaltose (Monofer®/Monoferric®)

ClinicalTrials.gov ID: NCT02962648

Public ClinicalTrials.gov record NCT02962648. 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 22, 2026, 9:18 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

An Open-label, Multicentre, Extension Trial to Assess the Safety of Re-dosing of Intravenous Iron Isomaltoside/Ferric Derisomaltose (Monofer®/Monoferric®)

Study identification

NCT ID
NCT02962648
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pharmacosmos A/S
Industry
Enrollment
103 participants

Conditions and interventions

Interventions

  • Iron isomaltoside/ferric derisomaltose 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
Jan 8, 2017
Primary completion
Jun 11, 2018
Completion
Jun 11, 2018
Last update posted
Mar 9, 2020

2017 – 2018

United States locations

U.S. sites
22
U.S. states
7
U.S. cities
18
Facility City State ZIP Site status
Pharmacosmos Investigational Site Chula Vista California 91910
Pharmacosmos Investigational Site 1 La Mesa California 91942
Pharmacosmos Investigational Site 2 La Mesa California 91942
Pharmacosmos Investigational Site Northridge California 91324
Pharmacosmos Investigational Site Porterville California 93257
Pharmacosmos Investigational Site Doral Florida 33172
Pharmacosmos Investigational Site Hialeah Florida 33012
Pharmacosmos Investigational Site Miami Florida 33135
Pharmacosmos Investigational Site Miami Florida 33147
Pharmacosmos Investigational Site Miami Florida 33165
Pharmacosmos Investigational Site Miami Lakes Florida 33014
Pharmacosmos Investigational Site West Palm Beach Florida 33409
Pharmacosmos Investigational Site Baton Rouge Louisiana 70808
Pharmacosmos Investigational Site Metairie Louisiana 70006
Pharmacosmos Investigational Site New Orleans Louisiana 70125
Pharmacosmos Investigational Site Shreveport Louisiana 71101
Pharmacosmos Investigational Site Plainsboro New Jersey 08536
Pharmacosmos Investigational Site Albuquerque New Mexico 87109
Pharmacosmos Investigational Site Chattanooga Tennessee 37404
Pharmacosmos Investigational Site Houston Texas 77030
Pharmacosmos Investigational Site 1 San Antonio Texas 78215
Pharmacosmos Investigational Site 2 San Antonio Texas 78215

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 NCT02962648, 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 Mar 9, 2020 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02962648 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →