Senti Biosciences, Inc. (Nasdaq: SNTI) (“Senti Bio”), a
biotechnology company innovating next-generation cell and gene
therapies using its proprietary Gene Circuit platform, today
reported financial results for the first quarter of 2023.
“I’m excited by the progress the team has made this
year as Senti transitions to a clinical stage company,” said
Timothy Lu, MD, PhD, Chief Executive Officer and Co-Founder of
Senti Bio. “Our recent preclinical data on SENTI-202 and other Gene
Circuit-enabled programs support the continued development of our
platform. Additionally, our upcoming presentations at ASGCT will
highlight preclinical data from collaborations with our partners,
and reinforce the application of Senti's Gene Circuits including
the NOT gates in multiple modalities, such as T cells, AAVs, and
iPSCs.”
RECENT PIPELINE HIGHLIGHTS
CAR-NK Cell Programs
SENTI-202: A Logic Gated
off-the-shelf CAR-NK cell therapy program designed to selectively
target and eliminate CD33 and/or FLT3 expressing hematologic
malignancies, such as acute myeloid leukemia (AML) and
myelodysplastic syndrome (MDS), while sparing healthy cells via a
NOT logic gate.
- Last month, at the American Association for Cancer Research
(AACR) Annual Meeting, the Company presented new preclinical data
on SENTI-202, demonstrating the in vitro ability to maintain colony
formation potential in hematopoietic stem cells (HSCs) that would
otherwise be killed in the absence of the NOT logic gate. The data
also showed that SENTI-202 chimeric antigen receptor natural killer
(CAR-NK) cells demonstrated increased cytotoxic activity, serial
killing, and cytokine production compared to unengineered NK cells
within in vitro and in vivo AML models, as well as killing of
primary tumor-derived samples from AML, including leukemic stem
cells, and MDS patients.
- Senti Bio remains on track to file an Investigational New Drug
(IND) application for SENTI-202 in patients with CD33 and/or FLT3
expressing hematologic malignancies in the second half of 2023 with
the planned Phase 1 trial focusing on relapsed/refractory patients
including AML.
SENTI-401: A Logic Gated,
Multi-Armed off-the-shelf selective CAR-NK cell therapy program
designed to precisely target CEA positive solid tumors (e.g.,
colorectal cancer) while sparing healthy cells via a NOT logic
gate.
- Senti Bio will present preclinical data at the upcoming
American Society of Gene and Cell Therapy (ASGCT) Annual Meeting on
SENTI-401, demonstrating that automated high throughput screening
can optimize Gene Circuits in primary NK cells to achieve high
protection of healthy cells using the NOT Logic Gate while
maintaining effective killing against cancer cells.
- The Company was also able to show the ability of the Gene
Circuit platform to evaluate and rank the performance of hundreds
of gene circuits with different iCARs in parallel, in one
self-contained, concurrent, end-to-end process.
SENTI-301A: A Multi-Armed
off-the-shelf CAR-NK cell therapy development candidate designed
for the treatment of GPC3 expressing tumors, including
hepatocellular carcinoma (HCC).
- Senti Bio presented new pre-clinical data at AACR showing
serial killing of GPC3 expressing gastric cancer cell lines by
SENTI-301A, along with in vitro and in vivo activity against GPC3
expressing hepatocellular carcinoma.
- The Company is continuing to actively pursue strategic
geographical partnerships for clinical development of SENTI-301A.
Senti Bio believes that there is significant market opportunity for
SENTI-301A in various Asian territories where HCC is more
prevalent, and the Company is looking for regional collaboration
opportunities for further development of the program.
Collaboration Programs
Last week, Senti Bio announced that the company
will have multiple data presentations at the upcoming ASGCT Annual
Meeting. Importantly, the presentations will showcase the Company’s
initial preclinical data from its ongoing collaborations with
BlueRock Therapeutics (BlueRock) and Spark Therapeutics
(Spark).
- BlueRock
Collaboration: Two
presentations reinforcing Senti Bio’s proprietary Gene Circuit
platform, demonstrating the application of Smart Sensors and
Regulator Dials in induced pluripotent stem cells (iPSCs). The
company aims to highlight preclinical data around Tamoxifen
controlled Regulator Dial performance and the discovery and
validation of M1-state specific promoters as it relates to the
BlueRock collaboration.
- Spark
Collaboration: One
poster presentation validating the use of Senti Bio’s gene
circuitry in AAV-based delivery systems. The data will demonstrate
the application of the Company’s Smart Sensors to uncover highly
compact promoters that retain strong selectivity for
photoreceptors, which may be applicable to drive expression
cassettes encoding large transgenes for ocular diseases.
Manufacturing
In March, the Company announced that it initiated
technology transfer to its Alameda current good manufacturing
practice (cGMP) facility to support clinical-scale manufacturing
for the Company’s CAR-NK cell development candidates. Senti Bio
expects to complete this transfer prior to submitting the IND
application for SENTI-202.
- Additionally, Senti Bio can leverage its 92,000 square foot
Alameda facility and potentially monetize the property under
suitable circumstances.
FIRST QUARTER 2023 FINANCIAL
RESULTS
- As of March 31, 2023, Senti Bio held cash, cash equivalents and
short-term investments of $76.1 million, which the Company believes
is sufficient to fund operations through at least the first quarter
of 2024.
- Research & development expenses were $11.3 million for the
quarter ended March 31, 2023, compared to $7.6 million for the same
period in 2022. The increase was related to increased headcount to
support preclinical development of Senti Bio’s wholly-owned
programs.
- General and administrative expenses were $9.8 million for the
quarter ended March 31, 2023, compared to $5.3 million for the same
period in 2022. The increase was driven by equity award grants in
connection with the SPAC transaction, as well as increased costs
associated with transitioning to a publicly traded company.
- Net loss was $18.7 million, or $0.42 per basic and diluted
share, for the quarter ended March 31, 2023.
Senti Biosciences,
Inc.Unaudited Selected Consolidated Balance Sheet
Data(in thousands)
|
|
|
|
|
March 31, |
|
December 31, |
|
2023 |
|
2022 |
|
|
|
|
Cash and cash equivalents |
$ |
31,600 |
|
$ |
57,621 |
Short-term investments |
|
44,506 |
|
|
40,942 |
Restricted cash |
|
3,551 |
|
|
3,366 |
Property and equipment,
net |
|
58,987 |
|
|
56,136 |
Operating lease right-of-use
assets |
|
17,905 |
|
|
18,418 |
Total assets |
|
161,425 |
|
|
180,792 |
Total liabilities |
|
49,085 |
|
|
53,529 |
Total stockholders’ equity
(deficit) |
|
112,340 |
|
|
127,263 |
|
|
|
|
|
|
|
|
|
|
|
|
Senti Biosciences,
Inc.Unaudited Consolidated Statements of
Operations(in thousands, except share and per share
data)
|
|
|
Three Months Ended |
|
March 31, |
|
|
2023 |
|
|
|
2022 |
|
|
|
|
|
Total revenue |
$ |
1,286 |
|
|
$ |
1,104 |
|
Operating expenses: |
|
|
|
Research and development |
|
11,318 |
|
|
|
7,603 |
|
General and administrative |
|
9,802 |
|
|
|
5,259 |
|
Total operating expenses |
|
21,120 |
|
|
|
12,862 |
|
Loss from operations |
|
(19,834 |
) |
|
|
(11,758 |
) |
Total other income (expense), net |
|
1,112 |
|
|
|
(50 |
) |
Net loss |
|
(18,722 |
) |
|
|
(11,808 |
) |
Other comprehensive loss |
|
2 |
|
|
|
— |
|
Comprehensive loss |
$ |
(18,720 |
) |
|
$ |
(11,808 |
) |
|
|
|
|
Net loss per share, basic and
diluted |
$ |
(0.42 |
) |
|
$ |
(3.72 |
) |
Weighted-average shares
outstanding, basic and diluted |
|
44,070,974 |
|
|
|
3,171,254 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
About Senti BioOur mission is to
create a new generation of smarter medicines that outmaneuver
complex diseases using novel and unprecedented approaches. To
accomplish this, we are building a synthetic biology platform that
may enable us to program next-generation cell and gene therapies
with what we refer to as Gene Circuits. These novel and proprietary
Gene Circuits are designed to reprogram cells with biological logic
to sense inputs, compute decisions and respond to their cellular
environments. We aim to design Gene Circuits to improve the
intelligence of cell and gene therapies in order to enhance their
therapeutic effectiveness, precision, and durability against a
broad range of diseases that conventional medicines do not readily
address.
Our synthetic biology platform utilizes
off-the-shelf chimeric antigen receptor natural killer (CAR-NK)
cells, outfitted with Gene Circuit technologies, to target
particularly challenging liquid and solid tumor oncology
indications. Our lead product candidate is SENTI-202 for the
treatment of CD33 and/or FLT3 expressing hematologic malignancies,
such as acute myeloid leukemia (AML) and myelodysplastic syndromes
(MDS). Additionally, our SENTI-401 program is being designed for
the treatment of colorectal cancer (CRC) and other CEA-positive
cancers. We have also demonstrated in preclinical studies the
potential breadth of our Gene Circuits in other modalities,
including T cells, adeno-associated viruses (AAVs) and induced
pluripotent stem cells (iPSCs), and diseases outside of oncology;
and we have executed partnerships with Spark Therapeutics and
BlueRock Therapeutics to advance these capabilities.
Forward-Looking StatementsThis
press release and document contain certain statements that are not
historical facts and are considered forward-looking statements
within the meaning of Section 27A of the Securities Act of 1933, as
amended, and Section 21E of the Securities Exchange Act of 1934, as
amended. These forward-looking statements generally are identified
by the words “believe,” “could,” “predict,” “continue,” “ongoing,”
“project,” “expect,” “anticipate,” “estimate,” “intend,”
“strategy,” “future,” “opportunity,” “plan,” “may,” “should,”
“will,” “would,” “will be,” “will continue,” “will likely result,”
“forecast,” “seek,” “target” and similar expressions that predict
or indicate future events or trends or that are not statements of
historical matters. Forward-looking statements are predictions,
projections, and other statements about future events that are
based on current expectations of Senti Bio’s management and
assumptions, whether or not identified in this document, and, as a
result, are subject to risks and uncertainties. Forward-looking
statements include, but are not limited to, Senti Bio’s ability to
continue to advance its pipeline of preclinical programs and
product candidates, statements regarding Senti Bio’s research and
development activities, the release of additional preclinical data,
as well as statements about the potential attributes and benefits
of Senti Bio’s product candidates and platform technology. These
forward-looking statements are provided for illustrative purposes
only and are not intended to serve as and must not be relied on by
any investor as, a guarantee, an assurance, a prediction, or a
definitive statement of fact or probability. Actual events and
circumstances are difficult or impossible to predict and will
differ from assumptions. Many actual events and circumstances are
beyond the control of Senti Bio. Many factors could cause actual
future results to differ materially from the forward-looking
statements in this document, including but not limited to: (i)
changes in domestic and foreign business, market, financial,
political and legal conditions, (ii) changes in the competitive and
highly regulated industries in which Senti Bio operates, variations
in operating performance across competitors, changes in laws and
regulations affecting Senti Bio’s business, (iii) the ability to
implement business plans, forecasts and other expectations, (iv)
the risk of downturns and a changing regulatory landscape in Senti
Bio’s highly competitive industry, (v) risks relating to the
uncertainty of any projected financial information with respect to
Senti Bio, (vi) risks related to uncertainty in the timing or
results of Senti Bio’s preclinical studies, IND filings, and GMP
manufacturing startup activities, (vii) Senti Bio’s dependence on
third parties in connection with preclinical and IND-enabling
studies, IND filing, and GMP manufacturing buildout and startup
activities, (viii) risks related to delays and other impacts from
the COVID-19 pandemic, and (ix) the success of any future research
and development efforts by Senti Bio. The foregoing list of factors
is not exhaustive. You should carefully consider the foregoing
factors and the other risks and uncertainties described in the
“Risk Factors” section of Senti Bio’s registration statement on
Form S-1 (File No. 333-267390), filed with the SEC on September 12,
2022, and other documents filed by Senti Bio from time to time with
the SEC. These filings identify and address other important risks
and uncertainties that could cause actual events and results to
differ materially from those contained in the forward-looking
statements in this document. There may be additional risks that
Senti Bio does not presently know, or that Senti Bio currently
believes are immaterial that could also cause actual results to
differ from those contained in the forward-looking statements in
this document. Forward-looking statements speak only as of the date
they are made. Senti Bio anticipates that subsequent events and
developments may cause Senti Bio’s assessments to change. Except as
required by law, Senti Bio assumes no obligation to update publicly
any forward-looking statements, whether as a result of new
information, future events, or otherwise.
Availability of Other Information About
Senti Biosciences, Inc.For more information, please visit
the Senti Bio website at https://www.sentibio.com or follow Senti
Bio on Twitter (@SentiBio) and LinkedIn (Senti Biosciences).
Investors and others should note that we communicate with our
investors and the public using our company website
(www.sentibio.com), including, but not limited to, company
disclosures, investor presentations and FAQs, Securities and
Exchange Commission filings, press releases, public conference call
transcripts and webcast transcripts, as well as on Twitter and
LinkedIn. The information that we post on our website or on Twitter
or LinkedIn could be deemed to be material information. As a
result, we encourage investors, the media and others interested to
review the information that we post there on a regular basis. The
contents of our website or social media shall not be deemed
incorporated by reference in any filing under the Securities Act of
1933, as amended.
Find more information at sentibio.comFollow us on
LinkedIn and Twitter
Investor Contact: investors@sentibio.comMedia
Contact: Kelli Perkins, kelli@redhousecomms.com
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