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ACTIVE NOT RECRUITING Phase 2

Study of ARO-ANG3 in Participants With Homozygous Familial Hypercholesterolemia (HOFH)

NCT05217667 · View on ClinicalTrials.gov ↗

Study Summary

Participants with documented homozygous familial hypercholesterolemia (HoFH) who have provided informed consent will receive 2 open-label doses of ARO-ANG3 and be evaluated for safety and efficacy parameters through 36 weeks. Participants who complete the first 36 week treatment period may opt to continue in an additional 24-month extension period during which they will receive up to 8 doses open-label doses of ARO-ANG3.

Interventions

  • DRUG ARO-ANG 3 Injection

Study Locations (7)

Quebec

  • Research Site 2 — Chicoutimi
  • Research Site 1 — Québec

New York

  • Research Site 4 — Mount Sinai

Ohio

  • Research Site 5 — Cincinnati

New South Wales

  • Research Site 8 — Camperdown

Western Australia

  • Research Site 3 — Nedlands

Other

  • Research Site 7 — Johannesburg

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2022-04-22
Est. Completion 2025-11
Phase Phase 2

Sponsor

Arrowhead Pharmaceuticals

11 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT05217667

The ClinicalTrials.gov registry entry for NCT05217667 describes a study currently listed as active not recruiting. It is categorized as Phase 2, 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 18 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Arrowhead Pharmaceuticals, which has 11 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 Homozygous Familial Hypercholesterolemia appearing as the primary indexed condition, and to 1 intervention — of which ARO-ANG 3 Injection 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: NCT05217667 reports 7 study locations spanning 6 distinct geographic areas — top geographies include Quebec, New York, Ohio. 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 NCT05217667 about?

NCT05217667 is a clinical study titled "Study of ARO-ANG3 in Participants With Homozygous Familial Hypercholesterolemia (HOFH)". Participants with documented homozygous familial hypercholesterolemia (HoFH) who have provided informed consent will receive 2 open-label doses of ARO-ANG3 and be evaluated for safety and efficacy parameters through 36 weeks. Participants who complete the first 36 week treatment period may opt to co...

What is the current status of trial NCT05217667?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 18 participants. The study started on 2022-04-22. Estimated completion is 2025-11.

What conditions does trial NCT05217667 study?

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

What interventions are being tested in trial NCT05217667?

The interventions under investigation include: ARO-ANG 3 Injection (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT05217667?

This trial is sponsored by Arrowhead Pharmaceuticals, which has 11 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT05217667 being conducted?

This trial has 7 study locations across New York, Ohio, New South Wales, Western Australia, Quebec. 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