Silence also announced positive topline 36-week
data from ongoing phase 2 study of zerlasiran in patients with high
lipoprotein(a)
Company to host conference call and webcast
today at 8 a.m. EDT / 12 p.m. GMT
Silence Therapeutics plc, Nasdaq: SLN (“Silence” or “the
Company”), an experienced and innovative biotechnology company
committed to transforming people’s lives by silencing diseases
through precision engineered medicines, today reported its
financial results for the full year ended December 31, 2023, and
reviewed recent business highlights.
“2023 was a year of strong execution across Silence as we
advanced our proprietary pipeline in the clinic,” said Craig
Tooman, President and CEO of Silence. “That’s clearly bearing fruit
today with the positive topline 36-week data we announced from the
ongoing phase 2 study of zerlasiran in patients with high Lp(a). We
are excited about these data and the potential for zerlasiran to
address the needs of up to 1.4 billion worldwide living with high
Lp(a). In addition to zerlasiran, we’ve made excellent progress
advancing divesiran in PV and remain on-track to report phase 1
data by June. On the partnering side, we were pleased for
AstraZeneca to enter the clinic with the first product candidate
under our collaboration last month, further highlighting the
productivity of our mRNAi GOLD™ platform. We look forward to more
clinical data unfolding in the coming year from our proprietary
programs and building recognition of Silence as a true platform
company.”
Recent Business Highlights
Zerlasiran for cardiovascular disease
- In November 2023, reported positive topline data in multiple
dose portion of the APOLLO phase 1 study of zerlasiran in patients
with high Lp(a).
- Today announced positive topline 36-week data from the ongoing
ALPACAR-360 phase 2 study of zerlasiran in patients with a median
baseline Lp(a) of approximately 215 nmol/L. Zerlasiran was
administered at 300 mg subcutaneously every 16 or 24 weeks and 450
mg every 24 weeks.
- Study demonstrated highly significant reductions in Lp(a)
compared with placebo to week 36 (primary endpoint)
- Median percentage reduction in Lp(a) of 90% or greater were
observed for both doses at week 36
- No new safety concerns were identified during this treatment
period
- The 60-week study is ongoing and secondary endpoints, including
change in Lp(a) from baseline to week 48 (end of treatment period),
week 60 (end of study) and potential effects on other
lipids/lipoproteins, will be evaluated
- 48-week topline data expected in the second quarter of
2024
Divesiran for hematological diseases
- Advanced enrollment in the SANRECO phase 1/2 study of divesiran
in PV patients.
- Emerging data from the ongoing phase 1 open label portion of
the study continue to look promising
- On-track to report phase 1 data in the second quarter of
2024
Collaborations
- In February 2024, achieved a $10 million milestone following
the initiation of a phase 1 trial of the first product candidate
under AstraZeneca collaboration.
- In March 2024, Mallinckrodt notified Silence that they will not
pursue further development of SLN501 following the completion of
the phase 1 clinical trial. This will conclude all activities and
commitments under the collaboration agreement.
“We ended December 2023 with approximately $68.8 million and
significantly increased our cash position in early 2024 to over
$200 million,” said Rhonda Hellums, Chief Financial Officer of
Silence. “We are excited to have multiple programs advancing in the
clinic, supported by a substantial cash position that extends our
estimated runway into 2026. We also continue to evaluate partnering
opportunities that could provide additional non-dilutive funding
and further extend our cash runway. Looking ahead, we remain
committed to responsibly investing in initiatives that will advance
our pipeline and expand our platform into new targets where there
is clear unmet need and opportunity to deliver value to
patients.”
Financial Highlights for Year End 2023
- Cash Position: Cash and cash equivalents of £54.0
million ($68.8 million) as of December 2023, compared with £71.1
million as of December 31, 2022.
- Collaboration Revenue: Collaboration revenue was £25.4
million for the year ended December 31, 2023, and £17.5 million for
the year ended December 31, 2022, and related to research services
performed under the collaboration agreements with AstraZeneca,
Hansoh and Mallinckrodt.
- R&D Expenses: Research and development (R&D)
expenses were £44.0 million for the year ended December 31, 2023,
compared to £35.6 million for the year ended December 31, 2022. The
increase is a result of additional clinical studies and an increase
in contract manufacturing activities for Silence’s proprietary
programs.
- G&A Expenses: General and administrative (G&A)
expenses were £20.6 million for the year ended December 31, 2023,
compared to £19.6 million for the year ended December 31, 2022. The
increase is primarily due to non-cash stock compensation
costs.
- Net Loss: Net loss was £43.3 million, or 38.9 pence
basic and diluted net loss per share for the year ended December
31, 2023, compared to a net loss of £40.5 million, or 41.9 pence
basic and diluted net loss per share for the year ended December
31, 2022.
Post-Period Financial Highlights
- In January 2024, received total proceeds of approximately $30
million (includes approximately $20 million from ADS sales under
Silence’s Sales Agreement and approximately $10 million in R&D
tax credit).
- In February 2024, announced a private placement of ADSs with
gross proceeds of approximately $120 million (£94.5 million).
- In February 2024, achieved a $10 million clinical milestone
under AstraZeneca collaboration. This will be received in April
2024.
- Total ADSs outstanding were approximately 46,502,272, as of
March 1, 2024.
Cash and Liquidity Update
As of December 31, 2023, we had cash and cash equivalents of
£54.0 million ($68.8 million). With the addition of gross proceeds
from our private placement in February 2024 of $120 million
(approximately £94.4 million) before deducting fees and estimated
offering expenses, the $30 million from proceeds from sale of ADSs
under our ATM and receipt of our UK R&D tax credit, and the
receipt of the AstraZeneca $10 million milestone in the second
quarter of 2024, we believe that our cash of over $200 million and
anticipated milestones from current collaborations will be
sufficient to fund our operating expenses and capital expenditure
requirements into 2026. We may also achieve further milestones from
our current collaboration partners which will further extend our
cash runway.
Conference Call & Webcast Details
Company management will host a conference call and webcast
today, Wednesday, March 13, 2024, at 8 a.m. EDT / 12:00 p.m.
GMT.
Webcast link:
https://edge.media-server.com/mmc/p/rkramk2y
Conference call registration link:
https://register.vevent.com/register/BIa97253e879ff493bb6fe3a99a6ba3532
The conference call and webcast will also be archived on the
Company’s website at www.silence-therapeutics.com.
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 zerlasiran (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 divesiran
(SLN124) designed to address hematological diseases. Silence also
maintains ongoing research and development collaborations with
AstraZeneca 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 cash runway and forecast operating
cash flow, 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 “anticipate,”
“expect,” “intend,” “plan,” “believe,” “seek,” “estimate,” 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
on the date hereof. 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.
SILENCE THERAPEUTICS
plc
CONSOLIDATED INCOME
STATEMENTS
(in thousands, except for loss
per share)
2023
2022
2021
£000s
£000s
£000s
Revenue
25,375
17,501
12,415
Cost of sales
(10,318
)
(10,880
)
(7,456
)
Gross profit
15,057
6,621
4,959
Research and development costs
(44,025
)
(35,605
)
(30,765
)
General and administrative expenses
(20,636
)
(19,609
)
(20,008
)
Operating loss
(49,604
)
(48,593
)
(45,814
)
Finance and other expenses
(2,152
)
(47
)
(52
)
Finance and other income
1,446
1,272
10
Loss for the year before
taxation
(50,310
)
(47,368
)
(45,856
)
Taxation
7,043
6,879
6,446
Loss for the year after
taxation
(43,267
)
(40,489
)
(39,410
)
Loss per ordinary equity share (basic
and diluted)
(38.9) pence
(41.9) pence
(44.3) pence
SILENCE THERAPEUTICS
plc
CONSOLIDATED BALANCE
SHEETS
(in thousands)
December
31,
2023
2022
£000s
£000s
Non-current assets
Property, plant and equipment
1,813
2,201
Goodwill
7,840
8,009
Other intangible assets
284
320
Other long term assets
2,580
Financial assets at amortized cost
284
284
12,801
10,814
Current assets
Cash and cash equivalents
54,031
54,816
Financial assets at amortized cost
-
16,328
R&D tax credit receivable
17,627
14,882
Other current assets
9,135
9,745
Trade receivables
228
915
81,021
96,686
Non-current liabilities
Contract liabilities
(58,910
)
(63,485
)
Lease liability
(93
)
-
(59,003
)
(63,485
)
Current liabilities
Contract liabilities
(5,161
)
(8,864
)
Trade and other payables
(12,429
)
(12,633
)
Lease liability
(179
)
(446
)
(17,769
)
(21,943
)
Net assets
17,050
22,072
Capital and reserves attributable to
the owners of the parent
Share capital
5,942
5,390
Capital reserves
313,769
277,860
Translation reserve
1,951
2,085
Accumulated losses
(304,612
)
(263,263
)
Total shareholders equity
17,050
22,072
View source
version on businesswire.com: https://www.businesswire.com/news/home/20240313711941/en/
Inquiries: Silence Therapeutics plc Gem Hopkins, Head of
IR and Corporate Communications ir@silence-therapeutics.com Tel: +1
(646) 637-3208
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