Actively Recruiting

Phase 1
Phase 2
Age: 18Years +
All Genders
NCT07223658

Study of ARO-DIMERPA in Adult Participants With Mixed Hyperlipidemia

Led by Arrowhead Pharmaceuticals · Updated on 2026-01-09

78

Participants Needed

1

Research Sites

79 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Study to evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD), and effects on low-density lipoprotein cholesterol (LDL-C) and triglycerides (TGs) of single-dose ARO-DIMERPA and multiple doses of ARO-DIMERPA in adult participants with mixed hyperlipidemia.

CONDITIONS

Official Title

Study of ARO-DIMERPA in Adult Participants With Mixed Hyperlipidemia

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Willing to follow diet counseling as per Investigator judgment based on local standard of care
  • Specific fasting triglycerides, low-density lipoprotein cholesterol, and non-high density lipoprotein cholesterol levels at screening
  • Participants of childbearing potential must agree to use highly effective contraception plus condom during the study and for at least 90 days after the study or last study drug dose
  • Participants must not donate sperm or eggs during the study and for at least 90 days after the study or last study drug dose
Not Eligible

You will not qualify if you...

  • Current use or use within last 365 days or within 5 half-lives before Day 1 of any hepatocyte-targeted siRNA
  • Current use or use within last 90 days or within 5 half-lives before Day 1 of any antisense oligonucleotide therapy
  • Current use or use within last 60 days from Day 1 of any PCSK9 inhibitor monoclonal antibodies (eg, evolocumab or alirocumab)
  • Uncontrolled hypertension
  • History of bleeding diathesis or coagulopathy
  • Current diagnosis of nephrotic syndrome

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Research Site 1

Christchurch, New Zealand, 8011

Actively Recruiting

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Research Team

M

Medical Monitor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

2

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Study of ARO-DIMERPA in Adult Participants With Mixed Hyperlipidemia | DecenTrialz