Calidi Biotherapeutics, Inc. (“Calidi” or the “Company”), a
clinical-stage biotechnology company that is pioneering the
development of allogeneic cell-based delivery of oncolytic viruses,
and First Light Acquisition Group (“FLAG”) (NYSE American:
FLAG), a special purpose acquisition company organized to acquire
or merge with one or more businesses, today announced they have
entered into a definitive merger agreement to create a public
company focused on developing oncolytic viral therapies with stem
cell-based delivery platforms to treat a wide range of cancers with
significant unmet needs. Upon closing of the transaction,
anticipated to occur in the second quarter of 2023, the combined
company will be named Calidi Biotherapeutics, Inc. and led
by Allan Camaisa, CEO and Chairman of the Board. In addition,
the combined company’s common stock intends to list on the NYSE
American under the ticker “CLDI.”
Calidi Biotherapeutics is revolutionizing the clinical
development of first-in-class allogenic stem cell-based delivery
platforms to protect, deliver, and potentiate oncolytic viruses for
the treatment of cancer. Calidi’s technology directly addresses a
critical obstacle in traditional oncolytic virotherapy, overcoming
the oncolytic virus inactivation by a patient’s immune system
through an allogeneic stem cell delivery mechanism to successfully
target a wide range of cancers, including high-grade gliomas (HGG)
and solid tumors. Calidi’s pipeline includes two “off-the-shelf”
clinical programs, NeuroNova (CLD-101) and SuperNova (CLD-201),
which utilize allogeneic stem cell technologies loaded with either
vaccinia virus or adenovirus, being developed in partnership with
leading research institutions.
“We are excited to partner with FLAG which we believe will
accelerate our ability to bring life-changing therapies to
patients, pairing our first-in-class, allogeneic stem cell-based
technology with strategic partnering opportunities, to advance our
goal of revolutionizing cancer treatment,” said Allan Camaisa, CEO
and Chairman of the Board of Calidi Biotherapeutics. “This business
combination positions us well as we build upon the momentum
generated to date from our NeuroNova and SuperNova platforms, which
have the potential to overcome the limitations of first-generation
oncolytic virus therapies. Furthermore, the merger will allow us to
leverage FLAG’s comprehensive network in both the private and
public sectors, capital markets and operational experience, and
successful track record addressing missions of U.S. national and
global importance. We believe recent legislative progress
supporting federal funding for new cancer treatments provides an
immediate opportunity to showcase our combined synergy, where our
strong backgrounds align with a shared goal of bringing novel
therapeutic options to cancer patients in need.”
“We are very pleased to announce this merger with Calidi
Biotherapeutics as their differentiated technology shows potential
to enable improved quality of care, extend survival, and lower cost
of treatment in a market with a high unmet need,” said Tom
Vecchiolla, CEO of FLAG. “Our goal is to invest in people and
technologies that address the most important priorities and to
deliver results with national and global effect. We believe that
Calidi’s innovative technology offers a differentiated
immuno-oncology solution with a proprietary allogeneic stem
cell-based universal delivery system that harnesses the potential
of oncolytic viruses to address therapeutic needs in hard-to-treat
cancers.”
The transaction includes gross proceeds of up to $42 million in
trust with FLAG (assuming no redemptions by existing FLAG
shareholders). The parties will attempt to arrange a PIPE
Investment from institutional investors of up to $40 million.
Net proceeds from the transaction are expected to provide Calidi
with capital into the first half of 2025 to advance its pipeline of
therapeutic candidates through multiple clinical milestones,
including:
- NeuroNova (CLD-101): allogeneic neural stem
cells loaded with an oncolytic adenovirus for the treatment of HGG.
A completed open-label, Phase 1, dose-escalation clinical trial in
patients with newly diagnosed high-grade gliomas demonstrated that
CLD-101 was well tolerated and showed promising preliminary
clinical results of efficacy.In August 2022, City of Hope received
U.S. Food and Drug Administration (FDA) authorization to proceed
with another Phase 1 physician-sponsored clinical trial that will
use Calidi’s CLD-101 platform in patients with recurrent HGG. The
trial will assess the safety and tolerability of administering
serial doses of CLD-101 in adult patients with recurrent
histologically confirmed HGG (WHO grade III or IV). Secondary
endpoints will evaluate treatment efficacy, including
progression-free and overall survival as well as any immune
response. Interim clinical results are expected in the first half
of 2024.
- SuperNova (CLD-201): allogeneic
adipose-derived mesenchymal stem cells (AD-MSC) loaded with
tumor-selective CAL1 oncolytic vaccinia virus for the treatment of
advanced metastatic solid tumors. A previously conducted
physician-sponsored clinical trial using autologous adipose-derived
stromal cells demonstrated that CLD-201 was well tolerated and
showed early signs of efficacy in 24 patients with advanced solid
tumors and two patients with acute myeloid leukemia (AML).In
December 2022, Calidi was awarded $3.1 million from the California
Institute for Regenerative Medicine (CIRM) to support the clinical
development of CLD-201 through an Investigational New Drug (IND)
application, which the company anticipates submitting in the second
half of 2023. Additionally, Calidi expects interim results from a
CLD-201 Phase 1 trial in the first half of 2024.
- Proceeds from the transaction are also expected to support
expansion of Calidi’s stem cell-based delivery platforms into
additional indications
Key Transaction TermsUpon closing of the
business combination (the “Business Combination”), shareholders of
Calidi (assuming the conversion of all derivative securities other
than unvested options) will be entitled to receive 25,000,000
shares of FLAG common stock, subject to adjustments and after the
closing, shareholders of Calidi may be entitled up to 18,000,000
additional shares of FLAG common stock (the “Escalation Shares”)
during a five year period with incremental releases of 4,500,000
shares if the trading price of FLAG common stock is $12, $14, $16
and $18 for a period for any 20 days within any 30 consecutive day
trading period. Furthermore, holders of FLAG Class A common stock
who do not redeem their shares may be entitled to their pro rata
portion of up to an additional 2,000,000 shares of FLAG common
stock during a five-year period with incremental releases of up to
500,000 shares if the trading price of FLAG common stock is $12,
$14, $16 and $18 for a period for any 20 days within any 30
consecutive day trading period. Assuming no redemptions of shares
of FLAG by its public shareholders and a possible PIPE Investment
from institutional investors of up to $40 million, Calidi expects
to have cash and cash equivalents, prior to transaction expenses,
of up to $82 million and an anticipated pro forma enterprise
valuation of approximately $335 million.
The boards of directors of Calidi and FLAG unanimously approved
the proposed transaction, which is anticipated to close in the
second quarter of 2023. The closing of the transaction is subject
to the approval of FLAG shareholders, regulatory approval, a
minimum cash condition of $15 million, after the payment of
transaction expenses, and the satisfaction or waiver of certain
other customary closing conditions.
A Current Report on Form 8-K, filed by FLAG with the Securities
and Exchange Commission (SEC), will provide additional information
about the proposed business combination and will be available on
the SEC’s website at www.sec.gov. In addition, FLAG intends to
file a registration statement on Form S-4 with the SEC, including a
proxy statement/prospectus, and will file other documents regarding
the proposed transaction with the SEC.
AdvisorsLewis Brisbois Bisgaard & Smith LLP
acted as legal counsel to Calidi. Weil, Gotshal & Manges LLP
acted as legal counsel to FLAG.
About Calidi Biotherapeutics
Calidi Biotherapeutics is a clinical-stage immuno-oncology
company with proprietary technology that is revolutionizing the
effective delivery and potentiation of oncolytic viruses for
targeted therapy against difficult-to-treat cancers. Calidi
Biotherapeutics is advancing in clinical development a potent
allogeneic stem cell and oncolytic virus combination for use in
multiple oncology indications. Calidi’s off-the-shelf, universal
cell-based delivery platforms are designed to protect, amplify, and
potentiate oncolytic viruses currently in development leading to
enhanced efficacy and improved patient safety. Calidi
Biotherapeutics is headquartered in La Jolla, California. For
more information, please visit calidibio.com.
About First Light Acquisition Group
First Light Acquisition Group is a blank check company organized
for the purpose of effecting a merger, share exchange, asset
acquisition, share purchase, recapitalization, reorganization, or
other similar business combination with one or more businesses or
entities. The company is sponsored by a group of former industry
and federal leaders with extensive experience operating public
companies and organizations in highly regulated industries, and is
led by Thomas Vecchiolla, Chief Executive Officer of
FLAG.
Forward-Looking Statements
This press release contains forward-looking statements for
purposes of the “safe harbor” provisions under the United States
Private Securities Litigation Reform Act of 1995. Terms such as
“anticipates,” “believe,” “continue,” “could,” “estimate,”
“expect,” “intends,” “may,” “might,” “plan,” “possible,”
“potential,” “predicts,” “project,” “should,” “would” as well as
similar terms, are forward-looking in nature. The forward-looking
statements contained in this discussion are based on Calidi’s
current expectations and beliefs concerning future developments and
their potential effects. There can be no assurance that future
developments affecting Calidi will be those that it has
anticipated. These forward-looking statements involve a number of
risks, uncertainties (some of which are beyond Calidi’s control) or
other assumptions that may cause actual results or performance to
be materially different from those expressed or implied by these
forward-looking statements. Factors that may cause actual results
to differ materially from current expectations include, but are not
limited to: the occurrence of any event, change or other
circumstances that could give rise to the termination of
negotiations and any subsequent definitive agreements with respect
to the Business Combination with FLAG; the outcome of any legal
proceedings that may be instituted against FLAG, Calidi, the
combined company or others following the announcement of the
Business Combination, any private placement financing proposed to
be consummated concurrently with the Business Combination (the
“PIPE”), and any definitive agreements with respect thereto; the
inability to complete the Business Combination due to the failure
to obtain approval of the shareholders of FLAG, the inability to
complete any PIPE or other financing needed to complete the
Business Combination, or to satisfy other conditions to closing;
changes to the proposed structure of the Business Combination that
may be required or appropriate as a result of applicable laws or
regulations or as a condition to obtaining regulatory approval of
the Business Combination; the ability to meet stock exchange
listing standards following the consummation of the Business
Combination; the risk that the Business Combination disrupts
current plans and operations of Calidi as a result of the
announcement and consummation of the Business Combination; the
ability to recognize the anticipated benefits of the Business
Combination or to realize estimated pro forma results and
underlying assumptions, including with respect to estimated
shareholder redemptions; costs related to the Business Combination;
changes in applicable laws or regulations; the evolution of the
markets in which Calidi competes; the inability of Calidi to defend
its intellectual property and satisfy regulatory requirements; the
ability to implement business plans, forecasts, and other
expectations after the completion of the proposed Business
Combination, and identify and realize additional opportunities; the
risk of downturns and a changing regulatory landscape in the highly
competitive pharmaceutical industry; the impact of potential global
conflicts (including the current conflict in Ukraine) may have on
capital markets or on Calidi’s or FLAG’s business; the impact of
the COVID-19 pandemic on Calidi’s business; and other risks and
uncertainties set forth in the section entitled “Risk Factors” and
“Cautionary Note Regarding Forward-Looking Statements” in FLAG’s
final prospectus dated September 9, 2021 and Annual Report on Form
10-K for the year ended December 31, 2021, as filed with the
SEC on March 31, 2022, and the risks and uncertainties
indicated in the Registration Statement and the definitive proxy
statement to be delivered to FLAG’s shareholders, including those
set forth under “Risk Factors” therein, and other documents filed
or to be filed with the SEC by FLAG.
Additional Information and Where to Find It
FLAG intends to file with the SEC a registration statement on
Form S-4 (as may be amended from time to time, the “Registration
Statement”), which will include a preliminary proxy statement of
FLAG, and a prospectus in connection with the proposed business
combination transaction (the “Business Combination”) involving FLAG
and Calidi. The definitive proxy statement and other relevant
documents will be mailed to FLAG shareholders as of a record date
to be established for voting on the Business Combination. FLAG
securityholders and other interested persons are advised to read,
when available, the preliminary proxy statement/prospectus, and
amendments thereto, and the definitive proxy statement/prospectus
in connection with FLAG’s solicitation of proxies for the special
meetings to be held to approve the Business Combination because
these documents will contain important information about FLAG,
Calidi, and the Business Combination. Investors, securityholders
and other interested persons will also be able to obtain copies of
the Registration Statement, the proxy statement/prospectus and all
other relevant documents filed or that will be filed with the SEC
by FLAG, once such documents are filed, free of charge, on the
SEC’s website at www.sec.gov or by directing a request to: First
Light Acquisition Group, Inc., 11110 Sunset Hills Road #2278,
Reston, VA 20190.
Participants in the Solicitation
FLAG and Calidi and their respective directors and officers and
other members of management and employees may be deemed
participants in the solicitation of proxies in connection with the
proposed business combination. FLAG shareholders and other
interested persons may obtain, without charge, more detailed
information regarding directors and officers of FLAG in FLAG’s
Annual Report on Form 10-K for the year ended December 31,
2021, as filed with the SEC on March 31, 2021. Information
regarding the persons who may, under SEC rules, be deemed
participants in the solicitation of proxies from FLAG’s
shareholders in connection with the proposed business combination
will be included in the definitive proxy statement/prospectus that
FLAG intends to file with the SEC.
No Offer or Solicitation
This press release does not constitute (i) a solicitation
of a proxy, consent or authorization with respect to any securities
or in respect of the proposed Business Combination or (ii) an offer
to sell, a solicitation of an offer to buy, or a recommendation to
buy any security of Calidi, FLAG or any of their respective
affiliates. There shall not be any sale of any securities in any
state or jurisdiction in which such offer, solicitation, or sale
would be unlawful prior to registration or qualification under the
laws of such other jurisdiction. No offering of securities shall be
made except by means of a prospectus meeting the requirements of
Section 10 of the Securities Act of 1933, as amended, or an
exemption therefrom.
Contacts:
For Calidi:
Stephen Jasper
Gilmartin Group
stephen@gilmartinir.com
For First Light Acquisition Group:
Marybeth Wootton
ir@firstlightacquisition.com
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