HONG
KONG and GERMANTOWN, Md.
and SUZHOU, China, July 8, 2024
/PRNewswire/ -- Sirnaomics Ltd. (the "Company",
together with its subsidiaries, the "Group" or
"Sirnaomics"; stock code: 2257), a leading biopharmaceutical
company engaging in discovery and development of advanced RNAi
therapeutics, today announced the interim results for successful
completion of the second cohort of its Phase I clinical study of
GalNAc-based RNAi therapeutic STP122G, targeting Factor XI as a
novel form of anticoagulation agent.
The Cohort 2 is comprised of eight healthy participants who
completed dosing of 50 mg via subcutaneous administration and were
followed over a period of 140 days. Safety data showed there were
no dose-limiting toxicities or serious adverse events, with a dose
dependent target silencing activity, so the study will proceed to
the next dosing cohort. Sirnaomics plans to enroll up to a total of
five escalating dosing cohorts. The Phase I, multicentred,
randomized, double-blind, sequential cohort study is designed to
evaluate the safety, tolerability, pharmacokinetics and
pharmacodynamics of a single ascending dose of STP122G when
administered subcutaneously to healthy participants. The safety and
tolerability will be compared among five different doses of STP122G
(25 mg, 50 mg, 100 mg, 200 mg, 400 mg) to select one for future
studies. The target silencing activity and therapeutic benefit will
also be measured and compared for dose-dependent evaluation. The
study plans to recruit 40 total participants.
"STP122G is the first candidate based on the Group's GalAhead™
mxRNA technology targeting Factor XI for anticoagulation
application." said Dr. Patrick
Lu, Founder, Chairman of the Board, Executive Director,
President and Chief Executive Officer of Sirnaomics. "STP122G
may have a broad range of conditions that would benefit from a
novel form of anticoagulation therapy such as prevention of deep
vein thrombosis, treatment of atrial fibrillation for stroke
prevention, and treatment of pulmonary embolism. The clinical
studies with the first two cohorts of 16 healthy participants have
demonstrated an excellent safety profile and a dose-dependent
Factor XI silencing activities."
STP122G is a third-generation Factor XI inhibitor in cases of
prior treatments have not completely prevented bleeding for
patients with anticoagulant disorders. Factor XI is an enzyme
produced predominantly by hepatocytes in the liver and it plays an
important role in the body's blood clotting cascade. By inhibiting
Factor XI, STP122G may have a better safety profiles than current
anticoagulant drugs. There are three types of Factor XI inhibitors
currently on the market or in clinical trials: RNA-based, small
molecule, and monoclonal antibody treatments. As an RNA-based
treatment driven by Sirnaomics' GalAhead™ mxRNA delivery system,
STP122G targets the hepatocyte to inhibit the production of Factor
XI, which could offer long-term efficacy and less risk of
bleeding.
Additional information about this clinical trial is available at
clinicaltrials.gov using the identifier: NCT05844293.
About STP122G
STP122G is Sirnaomics' leading GalAhead™ mxRNA drug candidate,
targeting Factor XI for anticoagulation therapeutics. Sirnaomics
submitted a U.S. IND for STP122G in March
2023 and launched a Phase I clinical trial in April 2023 as part of the Group's Factor XI
Program. The Group launched the second cohort study in January 2024 and has seen an excellent safety
readout and a dose-dependent silencing activity of Factor XI. This
program is applicable across a broad range of disease indications
such as an anticoagulation, prevention and treatment of stroke
after atrial fibrillation, cancer after immunotherapy, and
improving total knee replacement recovery. STP122G is the inaugural
candidate utilizing Sirnaomics' proprietary GalNAc RNAi platform
technology, GalAhead™.
About Sirnaomics
Sirnaomics is an RNA therapeutics biopharmaceutical company with
product candidates in preclinical and clinical stages that focuses
on the discovery and development of innovative drugs for
indications with medical needs and large market opportunities.
Sirnaomics is the first clinical-stage RNA therapeutics company to
have a strong presence in both Asia and the United
States. Based on its proprietary delivery technologies:
Polypeptide Nanoparticle Formulation and the 2nd generation of
GalNAc conjugates, the Group has established an enriched drug
candidate pipeline. Sirnaomics is advancing RNAi therapeutics for
oncology application with multiple successes of its clinical
programs for STP705 and STP707. STP122G represents the first drug
candidate of GalAhead™ technology entering clinical development.
With the expansion of the Group's clinical pipeline and
establishment of the Group's manufacturing facility, Sirnaomics is
still focusing on a transition from a biotech company to a
biopharma corporation. Learn more at: www.sirnaomics.com.
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