ACC 2022: Late-breaking Science Video Collection
Published: 05 April 2022
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3088
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Overview
Full programme
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Views:
3088
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Likes:
7
ACC 22: Magnitude & Duration of Effects of a siRNA Targeting Lp(a)
- ACC 22: Findings from the VALOR-HCM Trial
- ACC 22: MAVA-LTE Shows Improvement in NYHA Class in Patients Treated with Mavacamten
- ACC 22: Results From the PACIFIC AF Trial
- ACC 22: FAME 3 Suggests CABG Outperforms FFR-Guided PCI in Patients with Multivessel Disease
- ACC 22: Results from the TRANSLATE-TIMI 70 Trial
- ACC 22: Results from the POISE-3 Trial
- ACC 22: ICD Shock Therapies and the Burden of Ventricular Tachycardia
- ACC 22: PACMAN-AMI Shows Reduced Plaque Regression in AMI Patients Treated with Alirocumab
- ACC 22: Magnitude & Duration of Effects of a siRNA Targeting Lp(a)
- ACC 22: Results From a sub-study of the POISE-3 Trial
- ACC 22: Findings from the CoreValve US Pivotal & SURTAVI Trials
- ACC 22: ADAPT-TAVR Shows SLT Does Not Affect CO for Patients After TAVR
- ACC 22: Results From the Chocolate-Touch Study
- ACC 22: Results from the GIPS-IV Trial
- ACC 22: FFR vs. IVUS-guided PCI in Intermediate Coronary Artery Stenosis: The FLAVOUR Trial
- ACC 22: Results From the EMPULSE Study – Empagliflozin Proves Beneficial for Patients With HF
- ACC 22: Secondary Analysis of CANTOS Finds LDL & HDL Predict Residual Risk of Atherosclerotic Events
- ACC 22: 3-year Efficacy Outcomes from the SPYRAL HTN-ON MED Med Pilot Study
- 2022 AHA/ACC/HFSA Guideline for HF Management: Highlights & Implementation
Overview
Our regular review series View from the Thoraxcenter hosted by Prof Nicolas Van Mieghem and Dr Joost Daemen (Thoraxcentre, Erasmus MC, Rotterdam, NL) provide a concise analysis of the late-breaking science results and spotlight impactful data.
For a deeper dive into key clinical trial data, Dr Harriette Van Spall (McMaster University, Hamilton, CA)talks with principal investigators in her regular Late-Breaker Discussion Series.
Short, accessible Expert Interviews were conducted with select faculty focusing on the results, applicability, and impact on future research.
More from this programme
Part 1
View from the Thoraxcenter
Part 2
Late-breaker Discussion Series
Part 3
Expert Interviews
Faculty Biographies
Transcript
Trial Rationale
So the Apollo Trial is designed to treat a lipid disorder that has been very resistant to treatment for a very long time and that's elevated Lipoprotein . About 20% of the world population have this lipid abnormality. And it is a cause for premature atherosclerotic cardiovascular disease and aortic stenosis. We really wanted to find treatments for it.
Mechanism of Action
What we studied is what's known as a short interfering RNA, it's a double stranded RNA and it's given subcutaneously. It is attached to a sugar that helps to transport it into the liver. It's taken up actively by the liver, is cleaved, and then one of the RNA strands degrades the messenger RNA that codes for the protein that's essential to the formation of lipoprotein.
Study Design and Inclusion Criteria
Well first of all this was a phase one trial so it's small. It was really designed primarily to look at safety but of course we do look carefully efficacy and we took people without known cardiovascular disease over the age of 18 men and women who had an elevated lipoprotein of at least 150 nanomoles per litre. And we ended up actually with the values even higher than that.
Key Findings
Well, first of all, key findings include we did not see any serious safety issues. The drug at the highest dose, we studied four different doses, at the highest dose it reduced lipoprotein by 98%. In the second to highest dose, it reduced it by 96%, but impressively, that effect was durable. And if you go on a 150 days, five months, was still 81% reduced in the top dose group and 70% reduced in the next highest dose group. So very effective lowering, very durable lowering.
Next Steps
So when you do these studies you have to plan the next phase, which is phase two. Right now we're doing what is known as a multiple dose study, where instead of giving a single dose, we give a couple of doses. We'll need to see what happens to the durability and to the efficacy when we give somewhat smaller doses but do it more than once. After that's completed we'll enter phase two and ultimately phase three.
Take-home Messages
This is part of the kind of routine approach to drug development. Take home message is that lipoprotein is important. It needs to be measured in more patients. There are therapies coming, the therapy we studied and at least two others. And ultimately this is that last frontier of a lipid disorder that we've never been able to treat and we're soon going to be able to treat.