Silence Therapeutics Announces Preliminary Single Dose Results from SLN124 Phase 1 Study in Patients with Thalassemia
September 29 2022 - 7:00AM
Business Wire
Silence Therapeutics plc, 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 preliminary results from the single dose component
of the GEMINI II phase 1 study of SLN124, a siRNA targeting the
TMPRSS6 gene, in 24 adults with non-transfusion dependent
thalassemia.
The primary objective of the single dose arm was to evaluate the
safety and tolerability of SLN124 subcutaneous dosing (1.0, 3.0 and
6.0 mg/kg) in alpha/beta-thalassemia patients. Following a single
dose, there were no serious adverse events, severe treatment
emergent adverse events (TEAEs) that were SLN124 related or TEAEs
leading to withdrawal. No dose limiting toxicities or drug related
liver injury were observed.
Pharmacokinetic (PK) parameters and pharmacodynamic (PD)
biomarkers of iron metabolism are being evaluated in the ongoing
multiple dose arm of the study which is anticipated to readout next
year. This includes effects on hepcidin, serum iron, transferrin
saturation and hemoglobin.
“We are very encouraged by the excellent safety profile SLN124
continues to demonstrate and look forward to assessing PD effects
following the ongoing multiple dose part of the study,” said Giles
Campion, MD, Head of R&D and Chief Medical Officer at Silence.
“We remain excited about the potential for SLN124 to address a
range of hematological conditions, including polycythemia vera (PV)
which we plan to evaluate in a phase 1/2 study later this
year.”
SLN124 has rare pediatric disease and orphan drug designations
for beta-thalassemia as well as orphan drug designation for PV.
SLN124 was also granted FDA Fast Track Designation for PV earlier
this month.
About SLN124 SLN124 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,
SLN124 aims to temporarily ‘silence’ TMPRSS6, a gene that prevents
the liver from producing a particular hormone that controls iron
levels in the body – hepcidin. As hepcidin increases, iron levels
in the blood are expected to decrease, which could in turn allow
more healthy red blood cells to be produced, thereby improving
anemia. SLN124 has demonstrated proof of concept in healthy
volunteers and is being evaluated in a phase 1 study in patients
with non-transfusion dependent thalassemia. A phase 1/2 study in
polycythemia vera (PV) is planned for the second half of 2022.
SLN124 has rare pediatric disease and orphan drug designations for
beta-thalassemia as well as orphan drug designation for PV. SLN124
also has FDA Fast Track Designation for PV.
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 need. Silence's
proprietary mRNAi GOLD™ platform can be used to create siRNAs
(short interfering RNAs) 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
hematological conditions. Silence also maintains ongoing research
and development collaborations with AstraZeneca, Mallinckrodt
Pharmaceuticals, and Hansoh Pharma, 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 within the meaning
of the U.S. Private Securities Litigation Reform Act of 1995 and
other securities laws, including with respect to the Company’s
clinical and commercial prospects, regulatory approvals of the
Company’s product candidates, potential partnerships or
collaborations or payments under new and existing collaborations,
the initiation or completion of the Company’s clinical trials and
the anticipated timing or outcomes of data reports from the
Company’s clinical trials. These forward-looking statements are not
historical facts but rather are based on the Company's current
assumptions, beliefs, expectations, estimates and projections about
its industry. 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 those risks identified in the Company’s most recent
Admission Document and its Annual Report on Form 20-F filed with
the U.S. Securities and Exchange Commission (the “SEC”) on March
17, 2022. 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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version on businesswire.com: https://www.businesswire.com/news/home/20220929005148/en/
Enquiries: Silence Therapeutics plc Gem Hopkins,
Head of IR and Corporate Communications ir@silence-therapeutics.com
Tel: +1 (646) 637-3208
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