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ACTIVE NOT RECRUITING Phase 3

Phase 3 Study of ALXN1850 Versus Placebo in Adolescent and Adult Participants With HPP Who Have Not Previously Been Treated With Asfotase Alfa

NCT06079281 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this study is to assess the efficacy of ALXN1850 versus placebo on functional outcomes in adolescent and adult participants with HPP who have not previously been treated with asfotase alfa.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG ALXN1850

Study Locations (20)

Other

  • Research Site — Ciudad de Buenos Aires
  • Research Site — Clayton
  • Research Site — Herston
  • Research Site — Parkville
  • Research Site — St Leonards
  • Research Site — Belo Horizonte
  • Research Site — Brasília
  • Research Site — Recife
  • Research Site — Salvador
  • Research Site — São Paulo
  • Research Site — São Paulo

Alberta

  • Research Site — Calgary
  • Research Site — Edmonton

Indiana

  • Research Site — Indianapolis

New York

  • Research Site — Garden City

North Carolina

  • Research Site — Durham

Ohio

  • Research Site — Columbus

Tennessee

  • Research Site — Nashville

Manitoba

  • Research Site — Winnepeg

Trial Details

FieldValue
Enrollment Target 124 participants
Start Date 2024-01-03
Est. Completion 2028-03-29
Phase Phase 3

Sponsor

Alexion Pharmaceuticals

109 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06079281

The ClinicalTrials.gov registry entry for NCT06079281 describes a study currently listed as active not recruiting. 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 124 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 2 interventions — of which Placebo 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: NCT06079281 reports 20 study locations spanning 9 distinct geographic areas — top geographies include Other, Alberta, 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 NCT06079281 about?

NCT06079281 is a clinical study titled "Phase 3 Study of ALXN1850 Versus Placebo in Adolescent and Adult Participants With HPP Who Have Not Previously Been Treated With Asfotase Alfa". The primary objective of this study is to assess the efficacy of ALXN1850 versus placebo on functional outcomes in adolescent and adult participants with HPP who have not previously been treated with asfotase alfa.

What is the current status of trial NCT06079281?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 124 participants. The study started on 2024-01-03. Estimated completion is 2028-03-29.

What conditions does trial NCT06079281 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 NCT06079281?

The interventions under investigation include: Placebo (DRUG), ALXN1850 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06079281?

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 NCT06079281 being conducted?

This trial has 20 study locations across Indiana, New York, North Carolina, Ohio, Tennessee. 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