Silence Therapeutics Reports Third Quarter 2022 Results
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.
- Net loss reduced to £7.1 million from £9.9 million in Q3 2021.
- Revenue increased to £3.4 million in Q3 2022, up from £3.2 million in Q3 2021, reflecting growth from collaboration agreements.
- FDA Fast Track Designation granted for SLN124 for polycythemia vera.
- Strong cash position of £90.0 million as of September 30, 2022, following a $56.5 million offering.
- Research and development expenses rose to £8.8 million in Q3 2022, up from £7.9 million in Q3 2021.
“Silence’s third quarter was one of strong execution across our business,” said
Third Quarter 2022 & Recent Highlights
mRNAi GOLD™ Proprietary Program Updates
SLN360 (cardiovascular disease)
-
Presented a new analysis from the APOLLO phase 1 single dose study of SLN360 in healthy adults with high lipoprotein(a), a key genetic risk factor for cardiovascular disease, in a moderated poster session at the
American Heart Association (“AHA”) 2022 Annual Meeting.-
Assessment showed participants who received a single dose of SLN360 maintained median Lp(a) reductions over
80% over a five-month period. Additionally, extension data to day 365 showed no new drug related safety findings.
-
Assessment showed participants who received a single dose of SLN360 maintained median Lp(a) reductions over
SLN124 (hematological diseases)
-
Reported preliminary single dose results from the GEMINI II phase 1 study of SLN124 in non-transfusion dependent thalassemia patients.
- Data showed no serious adverse events (“AEs”), no severe treatment emergent AEs that were SLN124 related and no TEAEs leading to withdrawal.
- No dose limiting toxicity or drug related liver injury was observed.
- Received FDA Fast Track Designation for SLN124 for the treatment of polycythemia vera (PV).
Anticipated Milestones
- SLN360 phase 2 study in patients with atherosclerotic cardiovascular disease (“ASCVD”) and high Lp(a) expected to start in the fourth quarter of 2022.
- SLN124 phase 1/2 study in PV patients expected to start in the fourth quarter of 2022.
Third Quarter 2022 Financial Results
For the three-month period ending
On
Revenue
Revenue recognized for the three months period ending
Cost of sales
Cost of sales increased
Research and Development
Research and development expenditure for the three months ended
General and Administrative
General and administrative expenses for the three-month period ended
Liquidity, cash and cash equivalents
As of
About
Forward-Looking Statements
Certain statements made in this announcement are forward-looking statements within the meaning of the
Condensed consolidated income statement (unaudited)
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Three months ended |
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Three months ended |
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Nine months ended |
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Nine months ended |
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|
|
|
|
|
|
' |
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' |
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' |
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' |
|
|
Revenue |
3,371 |
|
|
3,156 |
|
|
12,736 |
|
|
9,001 |
|
|
Cost of sales |
(2,394 |
) |
|
(2,052 |
) |
|
(7,021 |
) |
|
(5,414 |
) |
|
Gross profit |
977 |
|
|
1,104 |
|
|
5,715 |
|
|
3,587 |
|
|
Research and development expenses |
(8,771 |
) |
|
(7,916 |
) |
|
(27,206 |
) |
|
(23,541 |
) |
|
General and administrative expenses |
(5,827 |
) |
|
(5,472 |
) |
|
(16,141 |
) |
|
(14,597 |
) |
|
Operating loss |
(13,621 |
) |
|
(12,284 |
) |
|
(37,632 |
) |
|
(34,551 |
) |
|
Finance and other expenses |
(34 |
) |
|
(64 |
) |
|
(34 |
) |
|
(86 |
) |
|
Finance and other income |
4,329 |
|
|
296 |
|
|
5,348 |
|
|
8 |
|
|
Loss for the period before taxation |
(9,326 |
) |
|
(12,052 |
) |
|
(32,318 |
) |
|
(34,629 |
) |
|
Taxation |
2,223 |
|
|
2,123 |
|
|
5,592 |
|
|
4,653 |
|
|
Loss for the period after taxation |
(7,103 |
) |
|
(9,929 |
) |
|
(26,726 |
) |
|
(29,976 |
) |
|
Loss per ordinary equity share (basic and diluted) |
|
|
|
|
|
|
|
|
|
|
|
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Condensed consolidated balance sheet (unaudited)
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|
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|
|
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|
|
|
|
|
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Non-current assets |
|
|
|
|
|
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Property, plant and equipment |
|
2,319 |
|
|
1,944 |
|
|
|
7,958 |
|
|
7,592 |
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Other intangible assets |
|
20 |
|
|
24 |
|
Financial assets at amortized cost |
|
284 |
|
|
301 |
|
|
|
10,581 |
|
|
9,861 |
|
Current assets |
|
|
|
|
|
|
Cash and cash equivalents |
|
90,017 |
|
|
73,537 |
|
R&D tax credit receivable |
|
12,966 |
|
|
6,945 |
|
Other current assets |
|
10,343 |
|
|
5,520 |
|
Trade receivables |
|
130 |
|
|
331 |
|
|
|
113,456 |
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|
86,333 |
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Non-current liabilities |
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|
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Contract liabilities |
|
(63,973 |
) |
|
(72,501 |
) |
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|
(63,973 |
) |
|
(72,501 |
) |
Current liabilities |
|
|
|
|
|
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Contract liabilities |
|
(10,624 |
) |
|
(4,247 |
) |
Trade and other payables |
|
(14,810 |
) |
|
(10,783 |
) |
Lease liability |
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(499 |
) |
|
(137 |
) |
|
|
(25,933 |
) |
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(15,167 |
) |
Net(liabilities)/assets |
|
34,131 |
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|
8,526 |
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Capital and reserves attributable to the owners of the parent |
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|
|
|
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Share capital |
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5,384 |
|
|
4,489 |
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Capital reserves |
|
276,163 |
|
|
225,462 |
|
Translation reserve |
|
2,228 |
|
|
1,541 |
|
Accumulated losses |
|
(249,644 |
) |
|
(222,966 |
) |
Total shareholders (deficit)/equity |
|
34,131 |
|
|
8,526 |
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View source version on businesswire.com: https://www.businesswire.com/news/home/20221110005384/en/
Enquiries:
ir@silence-therapeutics.com
Tel: +1 (646) 637-3208
Source:
FAQ
What were Silence Therapeutics' financial results for Q3 2022?
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What key studies did Silence Therapeutics advance in Q3 2022?
What designations were awarded to SLN124?