Silence Therapeutics Announces Publication in Cardiovascular Research Highlighting the Emerging Potential of RNA Therapeutics in Preventing Lipoprotein(a)-Mediated Cardiovascular Disease
Silence Therapeutics plc (AIM:SLN, Nasdaq:SLN) has released a new review in Cardiovascular Research, focusing on RNA therapeutics for preventing cardiovascular disease linked to high lipoprotein(a) (Lp(a)) levels, a condition affecting around 20% of the global population. The review emphasizes RNA interference (RNAi) therapies, especially the lead candidate SLN360, which aims to lower Lp(a) levels significantly. Promising pre-clinical results indicate over 90% reduction in Lp(a) with a strong safety profile. Data from the ongoing APOLLO Phase 1 trial is expected in late 2021.
- SLN360 shows over 90% reduction in Lp(a) levels in pre-clinical studies.
- Strong safety profile indicated for SLN360.
- High Lp(a) affects approximately 1.4 billion people, representing a significant market opportunity.
- Anticipated data from the APOLLO Phase 1 trial in late 2021 may face delays.
Silence Therapeutics Announces Publication in Cardiovascular Research Highlighting the Emerging Potential of RNA Therapeutics in Preventing Lipoprotein(a)-Mediated Cardiovascular Disease
–High Lipoprotein(a) is a genetically determined cardiovascular risk factor affecting around
15 April 2021
LONDON, Silence Therapeutics plc, AIM:SLN and Nasdaq: SLN (“Silence” or “the Company”), a leader in the discovery, development and delivery of novel short interfering ribonucleic acid (siRNA) therapeutics for the treatment of diseases with significant unmet medical need, today announced a new review publication on the prevention of cardiovascular disease linked to high lipoprotein(a) – Lp(a) – levels in the latest issue of Cardiovascular Research, linked here.
The paper, authored by senior medical and scientific experts from both Silence and leading cardiology centers, explores the emerging potential of RNA interference (RNAi) therapeutics in lowering elevated levels of Lp(a), which are associated with higher cardiovascular risk compared to the general population. Published in the European Society of Cardiology’s research journal, the paper provides a timely assessment of current approaches to managing high Lp(a), which is estimated to affect around
Giles Campion, MD, EVP, Head of R&D and Chief Medical Officer of Silence Therapeutics said: “There is a growing body of evidence demonstrating high Lp(a) as a key predeterminant of cardiovascular disease, including premature heart attack and stroke. Unlike high cholesterol, which is a modifiable risk factor, high Lp(a) is a genetic risk factor that you cannot manage through diet or lifestyle changes. When considering a potential long-term preventative treatment for a large population, Lp(a)-lowering therapy must be safe, effective, well tolerated and conveniently administered. Our review explores the promising potential of RNAi therapies to fit that profile and address a major unmet need in cardiovascular disease.”
Silence is evaluating its wholly owned lead RNAi candidate, SLN360, for the treatment of high Lp(a) levels in the ongoing global APOLLO Phase 1 trial. In pre-clinical studies to date, SLN360 has demonstrated sustained and deep reduction of Lp(a) serum levels (>
Enquiries:
| Silence Therapeutics plc Gem Hopkins, Head of IR and Corporate Communications ir@silence-therapeutics.com | Tel: +1 (646) 637-3208 |
| Investec Bank plc (Nominated Adviser and Broker) Daniel Adams/Gary Clarence | Tel: +44 (0) 20 7597 5970 |
| European PR Consilium Strategic Communications Mary-Jane Elliott/ Angela Gray / Chris Welsh silencetherapeutics@consilium-comms.com | Tel: +44 (0) 20 3709 5700 |
About SLN360
Silence’s wholly owned lead product candidate, SLN360, is a gene ‘silencing’ therapy – one that is designed to temporarily block a specific gene’s message that would otherwise trigger an unwanted effect. In this case, it aims to ‘silence’ LPA, a gene that tells the body to make a specific protein that is only found in Lp(a). By silencing the LPA gene, the levels of Lp(a) are lowered, which in turn is expected to lower the risk of heart diseases, heart attacks and strokes.
About Lipoprotein(a)
Lipoprotein(a), known as Lp(a) for short, is a particle made by the liver, which consists of cholesterol, fats and proteins. Most people have some Lp(a) in their body, but about 1 in 5 people have high levels of Lp(a), because of a specific gene variation in their DNA. Most people are unaware if they have elevated Lp(a). People living with elevated Lp(a) have a higher risk of developing early heart disease, heart attacks and strokes. Most standard cholesterol tests do not currently include screening for Lp(a). Current medicines that are used to lower other lipid levels in the blood do not have a meaningful effect on Lp(a) and are less effective overall in people with high levels of Lp(a).
About Silence Therapeutics
Silence Therapeutics is developing a new generation of medicines by harnessing the body's natural mechanism of RNA interference, or RNAi, to inhibit the expression of specific target genes thought to play a role in the pathology of diseases with significant unmet medical need. Silence's proprietary mRNAi GOLD™ platform can be used to create siRNAs that precisely target and silence disease-associated genes in the liver, which represents a substantial opportunity. Silence's wholly owned product candidates include SLN360 designed to address the high and prevalent unmet medical need in reducing cardiovascular risk in people born with high levels of lipoprotein(a) and SLN124 designed to address iron loading anemias. Silence also maintains ongoing research and development collaborations with AstraZeneca, Mallinckrodt Pharmaceuticals, and Takeda, among others. For more information, please visit https://www.silence-therapeutics.com/.
Forward-Looking Statements
Certain statements made in this announcement are forward-looking statements, including with respect to the Company’s clinical development timeline and commercial prospects. These forward-looking statements are not historical facts but rather are based on the Company's current expectations, estimates, and projections about its industry; its beliefs; and assumptions. Words such as 'anticipates,' 'expects,' 'intends,' 'plans,' 'believes,' 'seeks,' 'estimates,' and similar expressions are intended to identify forward-looking statements. These statements are not guarantees of future performance and are subject to known and unknown risks, uncertainties, and other factors, some of which are beyond the Company's control, are difficult to predict, and could cause actual results to differ materially from those expressed or forecasted in the forward-looking statements, including the potential impact of COVID-19 on the Company’s clinical development and regulatory timelines and plans. The Company cautions security holders and prospective security holders not to place undue reliance on these forward-looking statements, which reflect the view of the Company only as of the date of this announcement. The forward-looking statements made in this announcement relate only to events as of the date on which the statements are made. The Company will not undertake any obligation to release publicly any revisions or updates to these forward-looking statements to reflect events, circumstances, or unanticipated events occurring after the date of this announcement except as required by law or by any appropriate regulatory authority.
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