Inclisiran for Hypercholesterolemia
(SOLVE-LDL-C Trial)
Trial Summary
Will I have to stop taking my current medications?
The trial does not specify if you need to stop your current medications. However, it mentions that participants should be on five or more prescription drugs and on maximally tolerated statin therapy, which can be no statin if you have intolerance. It's best to discuss your specific medications with the trial team.
What data supports the effectiveness of the drug Inclisiran for treating hypercholesterolemia?
Inclisiran has been shown to significantly lower LDL cholesterol (the 'bad' cholesterol) by about 50% in patients with high cholesterol, even when they are already on other cholesterol-lowering medications. It also helps reduce the risk of major heart-related events, making it an effective treatment for managing cholesterol levels and improving heart health.12345
Is Inclisiran safe for humans?
How is the drug Inclisiran different from other treatments for hypercholesterolemia?
Inclisiran is unique because it is a small interfering RNA drug that lowers bad cholesterol (LDL-C) by blocking the production of a protein called PCSK9, and it only needs to be administered twice a year. This infrequent dosing helps with medication adherence, making it different from other treatments like statins, which require daily intake.2391011
What is the purpose of this trial?
Drug-drug interactions often limit statin optimization in a population of patients prescribed cytochrome P3A4 inhibitors, which include immunosuppressive agents, protease inhibitors, and antifungals. These patients frequently have autoimmune conditions or rheumatologic disorders that require complex drug regimens and are often on low-dose statin therapy or no statin at all, resulting in suboptimal LDL levels despite increased cardiovascular (CV) risk.There is an unmet clinical need to improve LDL levels in this vulnerable patient population, which faces increased CV risk due to underlying conditions that also contribute to polypharmacy and multiple drug-drug interactions. This study is a randomized, open-label trial evaluating subcutaneous inclisiran plus standard of care for LDL-C lowering in high-risk primary prevention patients with multiple comorbidities (e.g., Type II diabetes, liver disease, chronic kidney disease, autoimmune disease, solid-organ transplant) who are taking five or more medications in which drug-drug interactions prevent optimization of statin therapy.
Research Team
Michael Wilkinson, MD
Principal Investigator
University of California, San Diego
Eric D Adler, MD
Principal Investigator
University of California, San Diego
Pam Taub, MD
Principal Investigator
University of California, San Diego
Antoinette Birs, MD
Principal Investigator
University of California, San Diego
Eligibility Criteria
This trial is for adults aged 18-85 with metabolic syndrome or hypercholesterolemia, taking five or more prescription drugs. It's aimed at those who can't fully use statins due to drug interactions, like people with Type II diabetes, liver disease, chronic kidney disease, autoimmune diseases, or organ transplants. Participants should have an elevated risk of heart disease and be willing to receive injections.Inclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Baseline
Baseline assessments and first dose of inclisiran for the intervention group
Treatment
Participants receive inclisiran injections at baseline, 3 months, and 9 months; standard of care continues for all
Follow-up
Participants are monitored for safety and effectiveness after treatment
Treatment Details
Interventions
- Inclisiran
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of California, San Diego
Lead Sponsor
Novartis
Industry Sponsor
Vasant Narasimhan
Novartis
Chief Executive Officer since 2018
MD from Harvard Medical School, Bachelor's in Biological Sciences from University of Chicago, Master's in Public Policy from John F. Kennedy School of Government
Shreeram Aradhye
Novartis
Chief Medical Officer since 2022
MD from Yale University, MSc in Clinical Epidemiology from University of Pennsylvania