Silverback Therapeutics, Inc. (Nasdaq: SBTX) (“Silverback”), a
biopharmaceutical company leveraging its proprietary ImmunoTAC
technology platform to develop systemically delivered, tissue
targeted therapeutics for the treatment of chronic viral
infections, cancer, and other serious diseases, today reported
financial results for the first quarter ended March 31, 2022 and
provided a business update.
“In the first quarter of 2022, we have made significant progress
in advancing the preclinical development of SBT8230, a
first-in-class antibody-drug conjugate that we believe has the
potential to drive functional cure in patients with chronic
hepatitis B (cHBV) by eliciting a liver-localized anti-viral
response,” said Laura Shawver, Ph.D., chief executive officer of
Silverback. “We believe that activating the immune response is an
important component of a functional cure and may be combined with
treatments that target the HBV life cycle to improve durability.
Our team is on track to complete a regulatory submission in the
fourth quarter of 2022, enabling the planned initiation of the
single ascending dose healthy volunteer cohort of the Phase 1 study
in the first quarter of 2023. We plan to report data from this
cohort in the second half of 2023.”
SBT8230 (ASGR1-TLR8 ImmunoTAC conjugate for chronic
HBV)
- Initiated Phase 1-enabling toxicology study for SBT8230 in
the first quarter of 2022 and on track to complete Phase 1
regulatory submission in the fourth quarter of 2022. Silverback
expects to open enrollment for the single ascending dose healthy
volunteer cohort of the Phase 1 study in the first quarter of 2023
and anticipates reporting data from this portion of the study in
the second half of 2023. SBT8230 is comprised of an ASGR1
monoclonal antibody conjugated to a TLR8 linker-payload. ASGR1 is
highly expressed in liver and is restricted in its expression to
this organ. SBT8230 is designed to elicit a liver-localized
anti-viral immune response and has the potential to improve the
therapeutic window observed with untargeted, orally administered
TLR8 agonists in cHBV, which have shown promise preclinically, but
have been limited by toxicities in the clinic associated with
immune activation in the gastrointestinal tract.
ImmunoTAC Discovery Programs
- Silverback continues to advance discovery programs, with an
update anticipated in the fourth quarter of 2022. Discovery
efforts are focused on evaluating and developing new antigen
binding domains specific for targets of interest (including
antibodies), next-generation linker technologies, and both agonist
and antagonist small molecule payloads, that may be combined to
create novel tissue-targeted antibody conjugates.
First Quarter Financial Results
For the first quarter ended March 31, 2022, Silverback reported
a net loss of $24.6 million, compared to a net loss of $18.9
million for the comparable period in 2021.
Research and development expenses for the first quarter ended
March 31, 2022 were $16.9 million, compared to $12.2 million for
the same period in 2021. The increase in the Company’s research and
development expenses in 2022 were primarily attributable to an
increase in direct costs related to preclinical research efforts,
including the Company’s SBT8230 program, and increases in
personnel-related expenses as operations grew in support of program
advances.
General and administrative expenses for the first quarter ended
March 31, 2022 were $7.8 million, compared to $6.6 million for the
same period in 2021. The increase in general and administrative
expenses in 2022 were primarily attributable to an increase in
personnel-related expenses, including increases in salaries,
bonuses, and stock-based compensation. The increase in general and
administrative expenses in 2022 was also due to an increase in
legal fees, professional fees, and other various general and
administrative expenses as we now operate as a public company.
As of March 31, 2022, Silverback reported cash, cash
equivalents, and investments of $298.1 million, compared to $319.1
million at December 31, 2021, which is expected to fund operating
expenses and capital expenditure requirements into the second half
of 2026. As of March 31, 2022, Silverback had 35,145,281 shares of
common stock outstanding.
About Silverback Therapeutics
Silverback Therapeutics, Inc. is a biopharmaceutical company
focused on leveraging its proprietary ImmunoTAC technology platform
to develop systemically delivered and tissue targeted therapeutics
for the treatment chronic viral infections, cancer, and other
serious diseases. Silverback’s platform enables the strategic
pairing of proprietary payloads that modulate key disease modifying
pathways with monoclonal antibodies directed at specific disease
sites. Silverback Therapeutics is located in Seattle, Washington.
To learn more, visit www.silverbacktx.com.
Forward-Looking Statements
This news release contains certain forward-looking statements
that involve risks and uncertainties that could cause actual
results to be materially different from historical results or from
any future results expressed or implied by such forward-looking
statements. Such forward-looking statements include statements
regarding, among other things, Silverback’s plans and ability to
bring new treatments to patients in need, including the progress
and expected timing of Silverback’s drug development programs and
planned clinical trials, the timing for data and program updates,
the potential benefits of SBT8230, the strength of Silverback’s
balance sheet and the adequacy of cash on hand. Factors that may
cause actual results to differ materially include the risk that
compounds that appeared promising in early research or preclinical
trials do not demonstrate safety and/or efficacy in later
preclinical studies or clinical trials, the risk that Silverback
may not obtain approval to market its product candidates,
uncertainties associated with regulatory filings and applications,
risks associated with reliance on third parties to successfully
conduct research, preclinical studies or clinical trials, the risks
associated with reliance on outside financing to meet capital
requirements, and other risks associated with the process of
discovering, developing and commercializing drugs that are safe and
effective for use as human therapeutics, and in the endeavor of
building a business around such drugs. You are urged to consider
statements that include the words "may," "will," "would," "could,"
"should," "believes," "estimates," "projects," "promise,"
"potential," "expects," "plans," "anticipates," "intends,"
"continues," "designed," "goal," or the negative of those words or
other comparable words to be uncertain and forward-looking. For a
further list and description of the risks and uncertainties that
Silverback faces, please refer to Silverback’s periodic and other
filings with the Securities and Exchange Commission, which are
available at www.sec.gov. Such forward-looking statements are
current only as of the date they are made, and Silverback assumes
no obligation to update any forward-looking statements, whether as
a result of new information, future events or otherwise.
Silverback Therapeutics,
Inc.
Condensed Balance
Sheets
(in thousands, except share
and par value data)
(unaudited)
March 31,
December 31,
2022
2021
Assets
Current assets:
Cash and cash equivalents
$
233,989
$
254,045
Short-term investments
19,858
—
Prepaid expenses and other current
assets
7,485
7,447
Total current assets
261,332
261,492
Long-term investments
43,973
64,780
Restricted cash
250
250
Right-of-use asset
4,484
4,733
Property and equipment, net
2,430
2,212
Total assets
$
312,469
$
333,467
Liabilities and stockholders’
equity
Current liabilities:
Accounts payable
$
2,631
$
2,078
Accrued expenses
11,054
11,727
Current portion of lease liability
1,123
1,087
Total current liabilities
14,808
14,892
Lease liability, net of current
portion
4,431
4,760
Total liabilities
19,239
19,652
Commitments and contingencies
Stockholders’ equity:
Preferred Stock, $0.0001 par value per
share; 10,000,000 shares authorized at March 31, 2022 and December
31, 2021; no shares issued and outstanding at March 31, 2022 and
December 31, 2021
—
—
Common stock, $0.0001 par value per share;
200,000,000 shares authorized at March 31, 2022 and December 31,
2021, 35,145,281 and 35,133,934 shares issued and 35,123,330 and
35,107,651 shares outstanding at March 31, 2022 and December 31,
2021, respectively
4
4
Additional paid-in capital
505,317
500,349
Accumulated other comprehensive loss
(1,248
)
(326
)
Accumulated deficit
(210,843
)
(186,212
)
Total stockholders’ equity
293,230
313,815
Total liabilities and stockholders’
equity
$
312,469
$
333,467
Silverback Therapeutics,
Inc.
Condensed Statements of
Operations and Comprehensive Loss
(in thousands, except share
and per share data)
(unaudited)
Three Months Ended March
31,
2022
2021
Operating expenses:
Research and development
$
16,897
$
12,239
General and administrative
7,801
6,646
Total operating expenses
24,698
18,885
Loss from operations
(24,698
)
(18,885
)
Interest income, net
67
18
Net loss
$
(24,631
)
$
(18,867
)
Unrealized loss on available-for-sale
securities
(922
)
—
Comprehensive loss
$
(25,553
)
$
(18,867
)
Net loss per share, basic and diluted
$
(0.70
)
$
(0.54
)
Weighted-average shares used in computing
net loss per share, basic and diluted
35,114,131
34,773,950
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version on businesswire.com: https://www.businesswire.com/news/home/20220512005266/en/
Investor Contact: Miguel Arcinas Silverback Therapeutics (206)
736-7946 ir@silverbacktx.com
Media Contact: Jason Spark Canale Communications (619) 849-6005
jason.spark@canalecomm.com
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