Cartesian Therapeutics Announces Approval of Conversion of Series A Convertible Preferred Stock and Plans to Effect Reverse Stock Split
March 28 2024 - 4:05PM
Cartesian Therapeutics, Inc. (NASDAQ: RNAC) (the “Company”), a
clinical-stage biotechnology company pioneering mRNA cell therapy
for autoimmune diseases, today announced results from a special
meeting of stockholders held March 27, 2024.
During the meeting, Cartesian stockholders
approved the issuance of shares of common stock upon conversion of
Cartesian’s Series A Non-Voting Convertible Preferred Stock. The
conversion of the majority of the shares of Series A Non-Voting
Convertible Preferred Stock will occur automatically on April 8,
2024 at 5:00 p.m., Eastern time, and the remaining shares of Series
A Non-Voting Convertible Preferred Stock remain subject to
beneficial ownership limitations described in Cartesian’s filings
with the Securities and Exchange Commission. In addition,
stockholders voted to approve a reverse stock split of Cartesian’s
issued and outstanding common stock. In conjunction with this
approval, a 1-for-30 reverse stock split of Cartesian’s outstanding
shares of common stock, par value $0.0001 per share, will be
effective after the closing of trading hours on April 4, 2024.
Information Regarding Reverse Stock
Split
Cartesian’s common stock will begin trading on a
reverse stock split-adjusted basis at the opening of market trading
on April 5, 2024. Following the reverse stock split, the Company’s
common stock will continue to trade on The Nasdaq Global Market
under the symbol “RNAC” with the new CUSIP number 816212302.
At the effective time of the reverse split,
every 30 issued and outstanding shares of the Company’s common
stock will automatically be combined into one issued and
outstanding share of the Company’s common stock without any change
in the par value per share. Fractional shares will not be issued in
connection with the reverse stock split. Stockholders who would
otherwise be entitled to receive a fractional share will be
entitled to receive a cash payment in lieu of such fractional
share. The reverse stock split will affect all stockholders
uniformly and will not alter any stockholder’s relative interest in
the Company’s equity securities, except for any adjustments for
fractional shares. In addition, proportionate adjustments will be
made to the number of shares underlying, and the exercise or
conversion prices of, the Company’s outstanding stock options and
warrants, and to the number of shares of common stock issuable
under the Company’s equity incentive plans, and to the conversion
ratio of the Company’s Series A Non-Voting Convertible Preferred
Stock, par value $0.0001 per share.
The reverse stock split will reduce the number
of issued and outstanding shares of the Company’s common stock from
approximately 165.5 million shares to approximately 5.5 million
shares before the automatic conversion of the Company’s Series A
Non-Voting Convertible Preferred Stock into common stock, or
approximately 17.8 million shares thereafter. The approximately
166.3 thousand shares of Series A Non-Voting Convertible Preferred
Stock that remain subject to beneficial ownership limitations will
be convertible into approximately 5.5 million shares of common
stock for a total of approximately 23.3 million shares of common
stock outstanding once converted.
About Cartesian
Therapeutics
Cartesian Therapeutics is a clinical-stage
company pioneering mRNA cell therapies for the treatment of
autoimmune diseases. The Company’s lead asset, Descartes-08, is a
potential first-in-class mRNA CAR-T in Phase 2b clinical
development for patients with generalized myasthenia gravis.
Additional Phase 2 studies are planned in systemic lupus
erythematosus under an allowed IND, as well as basket trials in
additional autoimmune indications. The Company’s clinical-stage
pipeline also includes Descartes-15, a next-generation, autologous
anti-BCMA mRNA CAR-T.
Forward Looking Statements
Any statements in this press release about the
future expectations, plans and prospects of the Company, including
without limitation, statements regarding the Company’s planned
reverse stock split and the timing thereof, the automatic
conversion and any future conversions of the Company’s Series A
Non-Voting Convertible Preferred Stock into common stock, the
impact of the reverse stock split on the Company’s stockholders,
including any adjustments that may result from the treatment of
fractional shares, the expected number of shares of common stock to
be issued and outstanding following the reverse stock split, the
potential of Descartes-08 and Descartes-15 and the Company’s other
product candidates to treat myasthenia gravis, systemic lupus
erythematosus, or any other disease, the anticipated timing or the
outcome of the FDA’s review of the Company’s regulatory filings,
and other statements containing the words “anticipate,” “believe,”
“continue,” “could,” “estimate,” “expect,” “hypothesize,” “intend,”
“may,” “plan,” “potential,” “predict,” “project,” “should,”
“target,” “would,” and similar expressions, constitute
forward-looking statements within the meaning of The Private
Securities Litigation Reform Act of 1995. Actual results may differ
materially from those indicated by such forward-looking statements
as a result of various important factors, including, but not
limited to, the following: the uncertainties inherent in the
initiation, completion and cost of clinical trials including proof
of concept trials, including uncertain outcomes, the availability
and timing of data from ongoing and future clinical trials and the
results of such trials, whether preliminary results from a
particular clinical trial will be predictive of the final results
of that trial and whether results of early clinical trials will be
indicative of the results of later clinical trials, the ability to
predict results of studies performed on human beings based on
results of studies performed on non-human subjects, the unproven
approach of the Company’s RNA Armory® technology, potential delays
in enrollment of patients, undesirable side effects of the
Company’s product candidates, its reliance on third parties to
conduct its clinical trials, the Company’s inability to maintain
its existing or future collaborations, licenses or contractual
relationships, its inability to protect its proprietary technology
and intellectual property, potential delays in regulatory
approvals, the availability of funding sufficient for its
foreseeable and unforeseeable operating expenses and capital
expenditure requirements, the Company’s recurring losses from
operations and negative cash flows, substantial fluctuation in the
price of the Company’s common stock, risks related to geopolitical
conflicts and pandemics and other important factors discussed in
the “Risk Factors” section of the Company’s most recent Annual
Report on Form 10-K and subsequently filed Quarterly Reports on
Form 10-Q, and in other filings that the Company makes with the
Securities and Exchange Commission. In addition, any
forward-looking statements included in this press release represent
the Company’s views only as of the date of its publication and
should not be relied upon as representing its views as of any
subsequent date. The Company specifically disclaims any intention
to update any forward-looking statements included in this press
release, except as required by law.
Contact Information:
Investor Relations:Melissa ForstArgot
Partnerscartesian@argotpartners.com
Media:David RosenArgot
Partnerscartesian@argotpartners.com
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