Pharma Pioneer

Silence Therapeutics Reports Further Phase 1 Zerlasiran Trial Results in JAMA for Patients with High Lipoprotein(a)

16 May 2024
2 min read

New findings reveal that zerlasiran, an innovative therapeutic developed by Silence Therapeutics plc, effectively reduces lipoprotein(a) (Lp(a)) levels and is well-tolerated in both single and multiple doses. Published in the Journal of the American Medical Association (JAMA), the APOLLO phase 1 study focused on subjects with baseline Lp(a) levels of 150 nmol/L or higher.

Zerlasiran, a short interfering RNA (siRNA), targets and reduces the body's production of Lp(a), a significant genetic risk factor for cardiovascular disease, affecting up to 20% of the global population. The study included 32 healthy participants and 36 patients with atherosclerotic cardiovascular disease (ASCVD) and elevated Lp(a) levels.

In the single ascending dose trial, healthy participants were administered either a placebo, 300 mg, or 600 mg dose of zerlasiran. ASCVD patients received two doses at varying intervals: placebo, 200 mg at 4-week intervals, or 300 mg or 450 mg at 8-week intervals. Safety and tolerability were the primary outcomes, while secondary outcomes assessed serum levels of zerlasiran and its impact on Lp(a) concentrations.

Results showed that zerlasiran was safe and well-tolerated. In healthy participants, median Lp(a) levels changed by +14% for placebo, −30% for 300 mg, and −29% for 600 mg over 365 days. For ASCVD patients, the maximal median changes after two doses were +7% for placebo, -97% for 200 mg, -98% for 300 mg, and -99% for 450 mg, with effects diminishing to 0.3%, -60%, -90%, and -89% respectively after 201 days.

Currently, zerlasiran is being tested in the ALPACAR-360 phase 2 study for subjects with baseline Lp(a) levels of 125 nmol/L or higher, who are at high risk of ASCVD events.

Silence Therapeutics continues to develop RNA interference (RNAi) therapies, aiming to address significant unmet medical needs. Their proprietary mRNAi GOLD™ platform creates siRNAs targeting disease-associated genes. Other product candidates include divesiran for hematological diseases like polycythemia vera. The company also collaborates with AstraZeneca and Hansoh Pharma.

How to obtain the latest research advancements in the field of biopharmaceuticals?

In the Synapse database, you can keep abreast of the latest research and development advances in drugs, targets, indications, organizations, etc., anywhere and anytime, on a daily or weekly basis. Click on the image below to embark on a brand new journey of drug discovery!

图形用户界面, 文本, 应用程序, 聊天或短信

描述已自动生成

Adagrasib-Cetuximab Combo Shows Activity in Post-Treated KRAS G12C-Mutated CRC Patients
Pharma Pioneer
4 min read
Adagrasib-Cetuximab Combo Shows Activity in Post-Treated KRAS G12C-Mutated CRC Patients
16 May 2024
The Phase 1/2 KRYSTAL-1 trial, sponsored by Mirati Therapeutics, Inc., a subsidiary of Bristol Myers Squibb, combined KRAZATI® (adagrasib) with cetuximab to treat this specific group of patients who had undergone prior treatment.
Read →
Seres Therapeutics Completes Patient Recruitment for Phase 1B SER-155 Trial in Allogeneic Hematopoietic Stem Cell Transplant Recipients
Pharma Pioneer
3 min read
Seres Therapeutics Completes Patient Recruitment for Phase 1B SER-155 Trial in Allogeneic Hematopoietic Stem Cell Transplant Recipients
16 May 2024
Seres Therapeutics, a pioneering company in the field of microbiome therapeutics, has recently announced the completion of enrollment for Cohort 2 in its Phase 1b clinical trial of SER-155.
Read →
Alkermes Reports Positive ALKS 2680 Phase 1b Results for Narcolepsy Type 2 and Hypersomnia
Pharma Pioneer
2 min read
Alkermes Reports Positive ALKS 2680 Phase 1b Results for Narcolepsy Type 2 and Hypersomnia
16 May 2024
Alkermes plc has reported positive findings from a phase 1b study of ALKS 2680, an oral orexin 2 receptor agonist, in patients with narcolepsy type 2 (NT2) and idiopathic hypersomnia (IH).
Read →
Medicenna Showcases Latest MDNA11 Monotherapy Outcomes from Phase 1/2 ABILITY-1 Trial at AACR's 2024 Annual Gathering
Pharma Pioneer
2 min read
Medicenna Showcases Latest MDNA11 Monotherapy Outcomes from Phase 1/2 ABILITY-1 Trial at AACR's 2024 Annual Gathering
16 May 2024
Medicenna Therapeutics Corp. has reported positive interim results from its Phase 1/2 ABILITY-1 study of MDNA11, a long-acting interleukin-2 (IL-2) super-agonist.
Read →
Get started for free today!
Accelerate Strategic R&D decision making with Synapse, PatSnap’s AI-powered Connected Innovation Intelligence Platform Built for Life Sciences Professionals.
Start your data trial now!
Synapse data is also accessible to external entities via APIs or data packages. Empower better decisions with the latest in pharmaceutical intelligence.