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ACTIVE NOT RECRUITING Phase 1

Study of RN0361in Adult Healthy Subjects and Adult Hypertriglyceridemic Subjects

NCT06471543 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics and immunogenicity of single doses of RN0361 in Adult healthy subjects and Adult Hypertriglyceridemic Subjects.

Interventions

  • DRUG RN0361

Study Locations (10)

Texas

  • Synergy Groups Medical — Houston
  • Tranquil — Webster

Queensland

  • University of the Sunshine Coast Clinical Trials — Morayfield
  • University of the Sunshine Coast Clinical Trials, Sippy Downs — Sippy Downs

Victoria

  • Altona Clinical Research — Altona N.
  • Nucleus Network Melbourne — Melbourne

Florida

  • TBC Research LLC, — Tamarac

Kentucky

  • Versailles Family Medicine / Avacare — Versailles

Minnesota

  • Axis Clinicals USA — Dilworth

Utah

  • Ogden Clinic, Mountain View / Avacare — Pleasant View

Trial Details

FieldValue
Enrollment Target 108 participants
Start Date 2024-09-30
Est. Completion 2026-08-26
Phase Phase 1

Sponsor

Ikaria Bioscience Pty

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06471543

The ClinicalTrials.gov registry entry for NCT06471543 describes a study currently listed as active not recruiting. It is categorized as Phase 1, 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 108 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ikaria Bioscience Pty, which has 1 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 Hypertriglyceridemia appearing as the primary indexed condition, and to 1 intervention — of which RN0361 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: NCT06471543 reports 10 study locations spanning 7 distinct geographic areas — top geographies include Texas, Queensland, Victoria. 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 NCT06471543 about?

NCT06471543 is a clinical study titled "Study of RN0361in Adult Healthy Subjects and Adult Hypertriglyceridemic Subjects". The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics and immunogenicity of single doses of RN0361 in Adult healthy subjects and Adult Hypertriglyceridemic Subjects.

What is the current status of trial NCT06471543?

This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 108 participants. The study started on 2024-09-30. Estimated completion is 2026-08-26.

What conditions does trial NCT06471543 study?

This clinical trial studies the following conditions: Hypertriglyceridemia, Familial Chylomicronemia Syndrome. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06471543?

The interventions under investigation include: RN0361 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06471543?

This trial is sponsored by Ikaria Bioscience Pty, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06471543 being conducted?

This trial has 10 study locations across Florida, Kentucky, Minnesota, Texas, Utah. 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