Evaluating plozasiran for treating severe hypertriglyceridemia in adults
Double-blind, Placebo-controlled, Phase 3 Study to Evaluate the Efficacy and Safety of Plozsiran in Adults With Severe Hypertriglyceridemia
This study is testing if a new injection called plozasiran can help adults with severe high triglyceride levels lower those levels safely over a year.
Quick facts
| Phase | Phase 3 |
|---|---|
| Study type | Interventional |
| Enrollment | 300 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Arrowhead Pharmaceuticals Industry-sponsored |
| Locations | 149 sites (Birmingham, Alabama and 148 other locations) |
| Trial ID | NCT06347016 on ClinicalTrials.gov |
What this trial studies
This Phase 3 study aims to assess the safety and efficacy of plozasiran injection in adults diagnosed with severe hypertriglyceridemia. Participants will be randomly assigned to receive either plozasiran or a placebo, with doses administered once every three months. The study will monitor participants for efficacy and safety over a 12-month period, after which they may have the option to continue in an open-label extension. The goal is to determine whether plozasiran can effectively lower triglyceride levels in this patient population.
Who should consider this trial
Good fit: Ideal candidates are adults with a confirmed diagnosis of severe hypertriglyceridemia and fasting triglyceride levels of 500 mg/dL or higher.
Not a fit: Patients who have used specific hepatocyte-targeted siRNA therapies within the past year may not benefit from this study.
Why it matters
Potential benefit: If successful, this treatment could significantly reduce triglyceride levels in patients with severe hypertriglyceridemia, potentially lowering their risk of cardiovascular events.
How similar studies have performed: While this approach is novel in its specific application, similar studies targeting triglyceride levels have shown promise in the past.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Established diagnosis of severe hypertriglyceridemia (SHTG) and prior documented evidence (medical history) of fasting TG levels of ≥500 mg/dL (≥5.65 mmol/L) * Mean fasting TG level ≥500 mg/dL (≥5.65 mmol/L) collected at 2 separate and consecutive visits at least 7 days apart and no more than 17 days apart during the screening period * Fasting low density lipoprotein-cholesterol (LDL-C) ≤130 mg/dL (≤3.37 mmol/L) at screening * Screening HbA1C ≤8.5% * Must be on standard of care lipid-lowering medications per local guidelines (unless documented as intolerant as determined by the Investigator) Exclusion Criteria: * Use of any hepatocyte-targeted small interfering ribonucleic acid (siRNA) that targets lipids and/or triglycerides within 365 days before Day 1 (except inclisiran, which is permitted). Administration of investigational drug and inclisiran must be separated by at least 4 weeks * Use of any other hepatocyte-targeted siRNA or antisense oligonucleotide molecule within 60 days or within 5-half-lives before Day 1 based on plasma pharmacokinetics (PK), whichever is longer (except inclisiran, which is permitted) * Known diagnosis of familial chylomicronemia syndrome (FCS) (type 1 Hyperlipoproteinemia) by documentation of confirmed homozygote or double heterozygote for loss-of-function mutations in type 1- causing genes * Body mass index \>45kg/m\^2 Note: Additional Inclusion/Exclusion criteria may apply per protocol
Where this trial is running
Birmingham, Alabama and 148 other locations
- Ascension St. Vincents Birmingham — Birmingham, Alabama, United States (Recruiting)
- IMC-Diagnostic and Medical Clinic LLC — Mobile, Alabama, United States (Recruiting)
- National Heart Institute — Beverly Hills, California, United States (Recruiting)
- Hope Clinical Research — Canoga Park, California, United States (Recruiting)
- National Institute of Clinical Research, Inc. — Huntington Beach, California, United States (Recruiting)
- Clinical Trials Research — Lincoln, California, United States (Recruiting)
- VA Long Beach Healthcare System — Long Beach, California, United States (Recruiting)
- FOMAT Medical Research — Oxnard, California, United States (Recruiting)
- Innovative Research of West Florida, Inc. — Clearwater, Florida, United States (Recruiting)
- Harmony Clinical Research — North Miami, Florida, United States (Recruiting)
- Cardiovascular Center of Sarasota Foundation for Research and Education — Sarasota, Florida, United States (Recruiting)
- Georgia Clinical Research, LLC — Lawrenceville, Georgia, United States (Recruiting)
- RNA America Health Sciences — Sugar Hill, Georgia, United States (Recruiting)
- Midwest Cardiovascular Research and Education Foundation — Elkhart, Indiana, United States (Recruiting)
- Ascension St. Vincent Heart Center — Indianapolis, Indiana, United States (Recruiting)
- The South Bend Clinic LLC — South Bend, Indiana, United States (Recruiting)
- Midwest Heart and Vascular Specialists — Overland Park, Kansas, United States (Recruiting)
- Cotton-O'Neil Clinical Research Center, Stormont-Vail West — Topeka, Kansas, United States (Recruiting)
- Southern Clinical Research Associates — Metairie, Louisiana, United States (Recruiting)
- Annapolis Internal Medicine — Annapolis, Maryland, United States (Recruiting)
- Elite Clinical Research — Jackson, Mississippi, United States (Recruiting)
- Methodist Physicians Clinic — Fremont, Nebraska, United States (Recruiting)
- Velocity Clinical Research — Norfolk, Nebraska, United States (Recruiting)
- Overlook Medical Center — Morristown, New Jersey, United States (Recruiting)
- Jack D. Weiler Hospital — Bronx, New York, United States (Recruiting)
- Icahn School of Medicine at Mount Sinai — New York, New York, United States (Recruiting)
- Northwell Health Physician Partners at Peconic — Riverhead, New York, United States (Recruiting)
- Triad Internal Medicine — Asheboro, North Carolina, United States (Recruiting)
- Wilmington Health — Wilmington, North Carolina, United States (Recruiting)
- Internal Medicine Care Beavercreek — Beavercreek, Ohio, United States (Recruiting)
- OhioHealth Riverside Methodist Hospital — Columbus, Ohio, United States (Recruiting)
- Lynn Health Science Institute — Oklahoma City, Oklahoma, United States (Recruiting)
- AMS Cardiology — Horsham, Pennsylvania, United States (Recruiting)
- Capital Area Research, LLC — Newport, Pennsylvania, United States (Recruiting)
- University of Pennsylvania — Philadelphia, Pennsylvania, United States (Recruiting)
- University of Pennsylvania — Philadelphia, Pennsylvania, United States (Recruiting)
- Piedmont Research Partners — Fort Mill, South Carolina, United States (Recruiting)
- Tribe Clinical Research — Greenville, South Carolina, United States (Recruiting)
- University Diabetes & Endocrine Consultants — Chattanooga, Tennessee, United States (Recruiting)
- Diabetes and Thyroid Center of Fort Worth — Fort Worth, Texas, United States (Recruiting)
- Juno Research LLC — Houston, Texas, United States (Recruiting)
- Care and Cure Clinic — Houston, Texas, United States (Recruiting)
- Spring Clinical Research — Houston, Texas, United States (Recruiting)
- Sugar Lakes Family Practice — Sugar Land, Texas, United States (Recruiting)
- Northwest Houston Clinical Research, PLLC — Tomball, Texas, United States (Recruiting)
- Crossroads Clinical Research — Victoria, Texas, United States (Recruiting)
- Cope Family Medicine — Bountiful, Utah, United States (Recruiting)
- Chrysalis Clinical Research — Saint George, Utah, United States (Recruiting)
- Manassas Clinical Research Center — Manassas, Virginia, United States (Recruiting)
- Roanoke Heart Institute — Roanoke, Virginia, United States (Recruiting)
+99 more sites — see ClinicalTrials.gov for the full list.
Study contacts
- Study coordinator: Medical Monitor
- Email: plozasiran@arrowheadpharma.com
- Phone: 626-304-3400
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.