Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED Phase 3

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

NCT03238911 · View on ClinicalTrials.gov ↗

Study Summary

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).

Interventions

  • DRUG Ferric carboxymaltose
  • DRUG Iron isomaltoside/ferric derisomaltose

Study Locations (16)

Florida

  • Pharmacosmos Investigational Site — Clearwater
  • Pharmacosmos Investigational Site — Miami
  • Pharmacosmos Investigational Site 1 — Miami
  • Pharmacosmos Investigational Site 2 — Miami
  • Pharmacosmos Investigational Site — Miami
  • Pharmacosmos Investigational Site — Miami

California

  • Pharmacosmos Investigational Site — Los Angeles
  • Pharmacosmos Investigational Site — Sacramento
  • Pharmacosmos Investigational Site — Santa Ana

Indiana

  • Pharmacosmos Investigational Site — Indianapolis

Kansas

  • Pharmacosmos Investigational Site — Wichita

Louisiana

  • Pharmacosmos Investigational Site — Metairie

Pennsylvania

  • Pharmacosmos Investigational Site — Lancaster

Texas

  • Pharmacosmos Investigational Site — Houston

Utah

  • Pharmacosmos Investigational Site — Orem

Trial Details

FieldValue
Enrollment Target 123 participants
Start Date 2017-10-24
Est. Completion 2018-06-19
Phase Phase 3

Sponsor

Pharmacosmos A/S

4 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03238911

The ClinicalTrials.gov registry entry for NCT03238911 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 123 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pharmacosmos A/S, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Iron Deficiency Anemia appearing as the primary indexed condition, and to 2 interventions — of which Ferric carboxymaltose is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03238911 reports 16 study locations spanning 9 distinct geographic areas — top geographies include Florida, California, Indiana. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03238911 about?

NCT03238911 is a clinical study titled "Incidence of Hypophosphatemia After Treatment With Iron Isomaltoside/Ferric Derisomaltose vs Ferric Carboxymaltose in Subjects With Iron Deficiency Anaemia". 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).

What is the current status of trial NCT03238911?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 123 participants. The study started on 2017-10-24. Estimated completion is 2018-06-19.

What conditions does trial NCT03238911 study?

This clinical trial studies the following conditions: Iron Deficiency Anemia, Iron Deficiency Anaemia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03238911?

The interventions under investigation include: Ferric carboxymaltose (DRUG), Iron isomaltoside/ferric derisomaltose (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03238911?

This trial is sponsored by Pharmacosmos A/S, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03238911 being conducted?

This trial has 16 study locations across California, Florida, Indiana, Kansas, Louisiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial