Welcome to our dedicated page for Silence Therapeutics Plc news (Ticker: SLN), a resource for investors and traders seeking the latest updates and insights on Silence Therapeutics Plc stock.
Silence Therapeutics Plc (SLN) delivers cutting-edge RNA interference therapies through its proprietary mRNAi GOLD platform, targeting cardiovascular conditions, hematologic disorders, and rare diseases. This news hub provides investors and researchers with essential updates on clinical developments, strategic partnerships, and scientific breakthroughs.
Access authoritative reporting on SLN's siRNA pipeline progress, including trial milestones and regulatory filings. Our curated collection features press releases about platform enhancements, licensing agreements, and peer-reviewed research findings – all critical for understanding the company's position in gene silencing therapeutics.
Key updates cover clinical trial phases, intellectual property developments, and collaborative research initiatives. Bookmark this page for real-time insights into how Silence Therapeutics' targeted RNAi approach is advancing precision medicine across multiple therapeutic areas.
Silence Therapeutics plc, trading under Nasdaq: SLN, has appointed J.P. Gabriel as Chief Technical Operations Officer following the retirement of Jørgen Wittendorff. Gabriel brings over 25 years of experience in supply chain and manufacturing, crucial for advancing the company's clinical pipeline. Silence focuses on RNA interference technology to target genetic diseases and has product candidates like SLN360 and SLN124. The company also collaborates with AstraZeneca and other firms to enhance its research initiatives.
Silence Therapeutics plc (NASDAQ: SLN) presented key updates on its SLN360 and SLN124 programs at the 41st Annual J.P. Morgan Healthcare Conference. The SLN360 phase 2 study for high-risk atherosclerotic cardiovascular disease has begun dosing, with enrollment completion expected by Q4 2023. Preliminary data from the phase 1 study indicate significant reductions in lipoprotein(a) levels. Additionally, the SLN124 phase 1/2 study for polycythemia vera is now enrolling participants, with data from thalassemia patients expected in Q4 2023. Silence anticipates a pivotal year ahead.
Silence Therapeutics, trading under the ticker SLN, will be presenting at the 41st Annual J.P. Morgan Healthcare Conference on January 12 at 9:45 a.m. PT. The presentation by Craig Tooman, CEO, highlights the company's commitment to innovative biotechnology solutions aimed at silencing diseases through RNA interference. A live webcast will be available on the Silence Therapeutics website, with an archived replay to follow after the event.
Silence is focusing on RNAi-based medicines and has ongoing collaborations with leading pharmaceutical companies.
Silence Therapeutics plc (Nasdaq: SLN) reported its Q3 2022 financial results, showcasing a net loss of £7.1 million, an improvement from £9.9 million in Q3 2021. Revenue rose to £3.4 million, driven by collaboration agreements. Key milestones include anticipated phase 2 studies for SLN360 and SLN124, with SLN124 receiving FDA Fast Track Designation. The company's cash position stood at £90.0 million following a successful offering raising $56.5 million in August. This reinforces the company’s commitment to advancing its innovative pipeline.
Silence Therapeutics plc (NASDAQ: SLN) announced that CEO Craig Tooman will present a business overview at the Jefferies London Healthcare Conference on Wednesday, November 16, at 8:00 a.m. GMT. The conference aims to highlight Silence's innovative RNA interference technology, which targets gene silencing to tackle diseases with significant unmet needs. The live presentation will be available via webcast on Silence's website, with an archived replay accessible after the event.
Silence Therapeutics has presented promising data from its APOLLO phase 1 study of SLN360, targeting elevated lipoprotein(a) (Lp(a)), a significant cardiovascular risk factor. Results showed that participants receiving 300 mg and 600 mg doses maintained median reductions in Lp(a) levels exceeding 80% over five months. Some maintained reductions of up to 50% of baseline at one year. No new safety concerns arose, suggesting SLN360's potential for infrequent dosing. The company plans to advance into a phase 2 study for patients with atherosclerosis in late 2022.
Silence Therapeutics plc, a leader in siRNA therapeutics, announced preliminary results from the GEMINI II phase 1 study of SLN124 targeting the TMPRSS6 gene in adults with non-transfusion dependent thalassemia. The study showed an encouraging safety profile with no serious adverse events or dose limiting toxicities. Pharmacokinetic and pharmacodynamic evaluations are ongoing, with results expected next year. SLN124 has received FDA Fast Track Designation for polycythemia vera, and a phase 1/2 trial is planned for later this year, showcasing its potential across various hematological conditions.
Silence Therapeutics plc (Nasdaq: SLN) announced that Giles Campion, MD, will participate in a fireside chat at the Chardan Genetic Medicines Conference on October 4 at 3:45 p.m. ET in New York. The event can be viewed live on the company's website. Silence Therapeutics focuses on developing innovative siRNA therapeutics targeting diseases with significant unmet medical needs, leveraging its mRNAi GOLD™ platform. Major products include SLN360 for cardiovascular risk and SLN124 for rare hematological diseases. Collaborations with AstraZeneca and others enhance their research efforts.
Silence Therapeutics, a leader in RNAi therapeutics, announced participation in two upcoming conferences in New York. The first is the Morgan Stanley Global Healthcare Conference, featuring a fireside chat on September 13, 2022, at 5:15 p.m. ET. The second is the H.C. Wainwright Global Investment Conference, with a fireside chat on September 14, 2022, at 4:00 p.m. ET. Investors can access webcasts of these chats on the company’s website. Silence focuses on developing siRNA therapeutics targeting diseases with significant unmet needs.
Silence Therapeutics has received Fast Track Designation from the FDA for SLN124, an siRNA targeting the TMPRSS6 gene, aimed at treating polycythemia vera (PV). This designation could accelerate the development and review process, enabling quicker patient access to treatments. SLN124 has shown proof of mechanism and tolerability in prior studies. The company also plans to initiate a phase 1/2 study this year and is evaluating SLN124 for other hematological diseases.