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RECRUITING

A Prospective Sub-Study of the Global Hypophosphatasia Registry

NCT05234567 · View on ClinicalTrials.gov ↗

Study Summary

In this prospective observational sub-study, participants with pediatric-onset hypophosphatasia (HPP) (perinatal/infantile- or juvenile-onset) of any age will be followed for a minimum of 5 years at sites in the United States and potentially 1 or 2 other countries.

Conditions Studied

Interventions

  • BIOLOGICAL Asfotase Alfa

Study Locations (12)

Ohio

  • Clinical Trial Site — Cincinnati
  • Clinical Trial Site — Columbus

Connecticut

  • Clinical Trial Site — Hartford

Illinois

  • Clinical Trial Site — Chicago

Massachusetts

  • Clinical Trial Site — Boston

Missouri

  • Clinical Trial Site — Kansas City

New York

  • Clinical Trial Site — Mineola

Pennsylvania

  • Clinical Trial Site — Pittsburgh

Tennessee

  • Clinical Trial Site — Nashville

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2022-08-25
Est. Completion 2028-07-18

Sponsor

Alexion Pharmaceuticals

109 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05234567

The ClinicalTrials.gov registry entry for NCT05234567 describes a study currently listed as recruiting. It is categorized as an unspecified phase, 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 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Alexion Pharmaceuticals, which has 109 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Hypophosphatasia appearing as the primary indexed condition, and to 1 intervention — of which Asfotase Alfa 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: NCT05234567 reports 12 study locations spanning 11 distinct geographic areas — top geographies include Ohio, Connecticut, Illinois. 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 NCT05234567 about?

NCT05234567 is a clinical study titled "A Prospective Sub-Study of the Global Hypophosphatasia Registry". In this prospective observational sub-study, participants with pediatric-onset hypophosphatasia (HPP) (perinatal/infantile- or juvenile-onset) of any age will be followed for a minimum of 5 years at sites in the United States and potentially 1 or 2 other countries.

What is the current status of trial NCT05234567?

This trial is currently recruiting. The enrollment target is 30 participants. The study started on 2022-08-25. Estimated completion is 2028-07-18.

What conditions does trial NCT05234567 study?

This clinical trial studies the following conditions: Hypophosphatasia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT05234567?

The interventions under investigation include: Asfotase Alfa (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05234567?

This trial is sponsored by Alexion Pharmaceuticals, which has 109 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05234567 being conducted?

This trial has 12 study locations across Connecticut, Illinois, Massachusetts, Missouri, New York. 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