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ACTIVE NOT RECRUITING Phase 3

The ENERGY 3 Study: Evaluation of Efficacy and Safety of INZ-701 in Children With ENPP1 Deficiency

NCT06046820 · View on ClinicalTrials.gov ↗

Study Summary

The primary purpose of Study INZ701-106 (The ENERGY 3 Study) is to assess the efficacy and safety of INZ-701 in children with ENPP1 Deficiency.

Interventions

  • DRUG INZ-701
  • DRUG Control Arm (Conventional Therapy)

Study Locations (15)

Other

  • Queensland Children's Hospital — South Brisbane
  • Centre Hospitalier Universitaire (CHU) Sainte-Justine — Montreal
  • Hôpital Bicêtre, Service d'endocrinologie et diabète de l'enfant (Childhood Endocrinology and Diabetes Department) — Le Kremlin-Bicêtre
  • King Faisal Specialist Hospital and Research Centre — Riyadh
  • Hospital San Joan de Deu — Barcelona
  • Umraniye Training and Research Hospital — Istanbul
  • Cukurova Universitesi Tip Fakultesi — Sarıçam
  • Al Jalila Children's Specialty Hospital — Dubai
  • Royal Manchester Children's Hospital — Manchester

Colorado

  • Children's Hospital of Colorado — Aurora

Illinois

  • Ann & Robert H. Lurie Children's Hospital — Chicago

Massachusetts

  • Boston Children's Hospital — Boston

Ohio

  • Nationwide Children's Hospital — Columbus

Pennsylvania

  • The Children's Hospital of Philadelphia — Philadelphia

Texas

  • Cook Children's Medical Center — Fort Worth

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2023-11-05
Est. Completion 2026-02
Phase Phase 3

Sponsor

Inozyme Pharma

6 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06046820

The ClinicalTrials.gov registry entry for NCT06046820 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 27 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Inozyme Pharma, which has 6 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Autosomal Recessive Hypophosphatemic Rickets appearing as the primary indexed condition, and to 2 interventions — of which INZ-701 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: NCT06046820 reports 15 study locations spanning 7 distinct geographic areas — top geographies include Other, Colorado, 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 NCT06046820 about?

NCT06046820 is a clinical study titled "The ENERGY 3 Study: Evaluation of Efficacy and Safety of INZ-701 in Children With ENPP1 Deficiency". The primary purpose of Study INZ701-106 (The ENERGY 3 Study) is to assess the efficacy and safety of INZ-701 in children with ENPP1 Deficiency.

What is the current status of trial NCT06046820?

This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 27 participants. The study started on 2023-11-05. Estimated completion is 2026-02.

What conditions does trial NCT06046820 study?

This clinical trial studies the following conditions: Autosomal Recessive Hypophosphatemic Rickets, Generalized Arterial Calcification of Infancy, Ectonucleotide Pyrophosphatase/Phosphodiesterase1 Deficiency. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06046820?

The interventions under investigation include: INZ-701 (DRUG), Control Arm (Conventional Therapy) (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06046820?

This trial is sponsored by Inozyme Pharma, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06046820 being conducted?

This trial has 15 study locations across Colorado, Illinois, Massachusetts, Ohio, Pennsylvania. 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