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Antisense Oligonucleotide
Olezarsen for High Triglycerides and Cardiovascular Disease
Phase 3
Waitlist Available
Research Sponsored by Ionis Pharmaceuticals, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Clinical diagnosis of atherosclerotic cardiovascular disease (ASCVD) or
a. Hypertriglyceridemia with fasting TG ≥200 mg/dL (2.26 millimoles per liter [mmol/L]) and <500 mg/dL (5.65 mmol/L) with either Clinical diagnosis of atherosclerotic cardiovascular disease (ASCVD) or At increased risk for ASCVD
Must not have
Estimated GFR < 30 mL/min/1.73 m^2
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
Pivotal Trial
Summary
This trial is testing olezarsen, a medication that lowers blood triglycerides by blocking a specific protein. It targets patients with high triglycerides and heart disease or severe high triglycerides. The goal is to see if it can help reduce heart disease risk.
Who is the study for?
This trial is for adults with high blood fat levels (triglycerides) and heart disease or at risk of it. They must be on stable heart medications for 4 weeks before joining. People with severe liver issues, very poor kidney function, or uncontrolled diabetes can't participate.
What is being tested?
The study tests Olezarsen's ability to lower fasting triglyceride levels compared to a placebo in patients with high triglycerides and heart disease or those at high risk. It aims to see if Olezarsen is more effective than no treatment.
What are the potential side effects?
Possible side effects of Olezarsen may include reactions at the injection site, changes in liver enzymes, reduced kidney function, low platelet counts, and potential allergic responses.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have been diagnosed with heart disease caused by hardened arteries.
Select...
I have high triglycerides and am at risk for heart disease.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
My kidney function is severely reduced.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Awards & Highlights
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: OlezarsenExperimental Treatment1 Intervention
Participants will be randomized to receive multiple doses of olezarsen, once every 4 weeks by subcutaneous (SC) injection up to Week 49.
Group II: PlaceboPlacebo Group1 Intervention
Participants will be randomized to receive olezarsen-matching placebo, once every 4 weeks by SC injection up to Week 49.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Olezarsen
2022
Completed Phase 3
~1810
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for high triglycerides include lifestyle changes, medications, and novel therapies like antisense oligonucleotides (ASOs). ASOs, such as Olezarsen, work by selectively inhibiting the production of apolipoprotein C-III, a protein that regulates triglyceride metabolism.
By reducing apolipoprotein C-III levels, these treatments lower triglyceride levels in the blood, which is crucial for patients with hypertriglyceridemia as it reduces the risk of atherosclerotic cardiovascular disease. Other treatments include fibrates, which activate peroxisome proliferator-activated receptors (PPARs) to increase the breakdown of triglycerides, and omega-3 fatty acids, which reduce triglyceride synthesis in the liver.
These mechanisms are important as they help manage and reduce the complications associated with high triglycerides.
Antisense therapy and emerging applications for the management of dyslipidemia.Antisense oligonucleotides as therapeutics for hyperlipidaemias.
Antisense therapy and emerging applications for the management of dyslipidemia.Antisense oligonucleotides as therapeutics for hyperlipidaemias.
Find a Location
Who is running the clinical trial?
Ionis Pharmaceuticals, Inc.Lead Sponsor
148 Previous Clinical Trials
14,031 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My kidney function is severely reduced.I have been diagnosed with heart disease caused by hardened arteries.I have high triglycerides and am at risk for heart disease.I have been on stable cholesterol medication for at least 4 weeks.You have a higher risk for developing cardiovascular diseases.Your liver enzymes are more than three times the normal level.Your HbA1c level is higher than 9.5% at the screening.You have very high levels of triglycerides in your blood after fasting.Your total bilirubin level is higher than what is considered normal, unless it's due to Gilbert's syndrome.
Research Study Groups:
This trial has the following groups:- Group 1: Placebo
- Group 2: Olezarsen
Awards:
This trial has 1 awards, including:- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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