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ARCA biopharma Announces 1-for-12 Reverse Stock Split in Connection with the Proposed Merger with Oruka Therapeutics Westminster, CO

Key Takeaway: ARCA biopharma has approved a 1-for-12 reverse stock split in anticipation of its merger with Oruka Therapeutics, expected to finalize on September 3, 2024. The action will reduce ARCA's outstanding shares significantly. Post-merger, the combined entity will trade under the new symbol 'ORKA'. Shareholders also approved an increase in authorized common stock from 100 million to 545 million shares, providing additional financial flexibility. However, potential risks and uncertainties surrounding the merger completion could impact investor sentiment.

Market Sentiment Analysis

POSITIVE FACTORS

  • Announced reverse stock split may improve stock price perception.
  • Merger with Oruka Therapeutics expected to benefit both companies.
  • Enhancement of authorized common stock may provide financial flexibility.

CONCERNS & RISKS

  • The substantial reverse stock split may lead to shareholder dissatisfaction.
  • Potential risks associated with the completion of the merger.
  • Uncertainties regarding the financial future and resource management post-merger.

Full Press Release Details

Announces 1-for-12 Reverse Stock Split in Connection with the Proposed Merger with Oruka Therapeutics
Westminster, CO, August 23, 2024
- ARCA biopharma, Inc. (NASDAQ: ABIO) ("ARCA") today announced that its Board of Directors (the "Board")
has approved a reverse stock split of ARCA's common stock at a ratio of 1-for-12. ARCA's common stock is expected to begin
trading on a post-reverse stock split basis on The Nasdaq Global Market on September 3, 2024, under the new name Oruka Therapeutics,
Inc. and under the new symbol "ORKA" following the anticipated closing of the merger with Oruka Therapeutics, Inc. (the "Merger"),
with a new CUSIP number 687604108 and ISIN number US6876041087.
The reverse stock split was approved
by ARCA's stockholders at ARCA's special meeting of stockholders held on August 22, 2024 (the "Special Meeting"),
to be effected in the Board's discretion of not less than 1-for-6 and not more than 1-for-12. The final reverse stock split ratio
of 1-for-12 was approved by the Board on August 22, 2024.
The reverse stock split is expected
to reduce the number of ARCA's outstanding common stock from approximately 14,507,143 shares to approximately 1,208,928 shares.
The number of shares of ARCA's authorized common stock will not be affected by the reverse stock split, but at the Special Meeting,
ARCA's stockholders approved an increase in the number of shares of ARCA's authorized common stock from 100,000,000 shares
to 545,000,000 shares in connection with the anticipated closing of the Merger. No fractional shares will be issued if, as a result of
the reverse stock split, a stockholder would otherwise become entitled to a fractional share because the number of shares of ARCA common
stock they hold before the reverse stock split is not evenly divisible by the split ratio. Instead, each stockholder will be entitled
to receive a cash payment in lieu of such fractional share. The cash payment to be paid will be equal to the fraction of a share to which
such stockholder would otherwise be entitled multiplied by the closing price per share as reported by The Nasdaq Stock Market LLC on September
As a result of the reverse stock split,
proportionate adjustments will made to the exercise prices and number of shares of ARCA's common stock underlying ARCA's
outstanding equity and warrant awards, and will become effective as of and contingent on the completion of the Merger, and to the number
of shares of common stock issuable or will be issuable upon conversion of ARCA's convertible preferred stock, including ARCA's
Series B non-voting convertible preferred stock to be issued in connection with the Merger. There will be no change to the par value
Following the closing of the Merger,
the combined company's total issued and outstanding common stock is expected to be approximately 29,490,443 shares, and there are
expected to be 5,430,360 shares of common stock underlying pre-funded warrants and 11,428,166 shares of common stock underlying ARCA's
Series B non-voting convertible preferred stock, representing a total of 46,348,969 common-stock equivalents (not including outstanding
employee and director equity awards).
is dedicated to developing genetically and other targeted therapies for cardiovascular diseases through a precision medicine approach
to drug development. For more information, please visit www.arcabio.com or follow the company on LinkedIn.
is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to
offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving
high rates of complete disease clearance with dosing as infrequently as one or twice a year. Oruka is advancing a proprietary portfolio
of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying
plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com.
contains forward-looking statements (including within the meaning of Section 21E of the Exchange Act and Section 27A of the
Securities Act) concerning ARCA, Oruka, the proposed transactions and other matters. These forward-looking statements include express
or implied statements relating to the structure, timing and completion of the proposed Merger; the combined company's listing on
Nasdaq after closing of the proposed Merger; expectations regarding the ownership structure of the combined company; the expected executive
officers and directors of the combined company; each company's and the combined company's expected cash position at the closing
of the proposed Merger (including completion of Oruka's private placement) and cash runway of the combined company; the expected
contribution and payment of dividends in connection with the Merger, including the timing thereof; the future operations of the combined
company; the nature, strategy and focus of the combined company; the development and commercial potential and potential benefits of any
product candidates of the combined company; anticipated preclinical and clinical drug development activities and related timelines, including
the expected timing for data and other clinical results; the combined company having sufficient resources to advance its pipeline candidates;
and other statements that are not historical fact. The words "anticipate," "believe," "contemplate,"
"continue," "could," "estimate," "expect," "intends," "may,"
"might," "plan," "possible," "potential," "predict," "project,"
"should," "will," "would" and similar expressions (including the negatives of these terms or variations
of them) may identify forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking.
These forward-looking statements are based on current expectations and beliefs concerning future developments and their potential effects.
There can be no assurance that future developments affecting ARCA, Oruka, including the pre-closing private financing, or the Merger
will be those that have been anticipated.
statements contained in this communication are based on current expectations and beliefs concerning future developments and their potential
effects and therefore subject to other risks and uncertainties. These risks and uncertainties include, but are not limited to, risks
associated with the possible failure to satisfy the conditions to the closing or consummation of the Merger risks associated with the
potential failure to complete the financing transaction in a timely manner or at all, risks associated with the uncertainty as to the
timing of the consummation of the Merger and the ability of each of ARCA and Oruka to consummate the transactions contemplated by the
Merger, risks associated with ARCA's continued listing on Nasdaq until closing of the Merger, the failure or delay in obtaining
required approvals from any governmental or quasi-governmental entity necessary to consummate the Merger; the occurrence of any event,
change or other circumstance or condition that could give rise to the termination of the Merger prior to the closing or consummation
of the Merger, risks associated with the possible failure to realize certain anticipated benefits of the Merger, including with respect
to future financial and operating results; the effect of the completion of the Merger on the combined company's business relationships,
operating results and business generally; risks associated with the combined company's ability to manage expenses and unanticipated
spending and costs that could reduce the combined company's cash resources; risks related to the combined company's ability
to correctly estimate its operating expenses and other events; changes in capital resource requirements; risks related to the inability
of the combined company to obtain sufficient additional capital to continue to advance its product candidates or its preclinical programs;
the outcome of any legal proceedings that may be instituted against the combined company or any of its directors or officers related
to the Merger Agreement or the transactions contemplated thereby; the ability of the combined company to obtain, maintain and protect
its intellectual property rights, in particular those related to its product candidates; the combined company's ability to advance
the development of its product candidates or preclinical activities under the timelines it anticipates in planned and future clinical
trials; the combined company's ability to replicate in later clinical trials positive results found in preclinical studies and
early-stage clinical trials of its product candidates; the combined company's ability to realize the anticipated benefits of its
research and development programs, strategic partnerships, licensing programs or other collaborations; regulatory requirements or developments
and the combined company's ability to obtain necessary approvals from the U.S. Food and Drug Administration or other regulatory
authorities; changes to clinical trial designs and regulatory pathways; competitive responses to the Merger and changes in expected or
existing competition; unexpected costs, charges or expenses resulting from the Merger; potential adverse reactions or changes to business
relationships resulting from the completion of the Merger; legislative, regulatory, political and economic developments; and those risks
and uncertainties and other factors more fully described in filings with the Securities and Exchange Commission ("SEC"),
including reports filed on Form 10-K, 10-Q and 8-K, in other filings that ARCA makes and will make with the
SEC in connection with the proposed Merger, including the Proxy Statement/Prospectus described below under "Important Additional
Information About the Proposed Transaction Filed with the SEC," and in other filings made by ARCA with the SEC from time to
time and available at www.sec.gov. These forward-looking statements are based on current expectations, and with regard to the proposed
transaction, are based on ARCA's current expectations, estimates and projections about the expected date of closing of the proposed
transaction and the potential benefits thereof, its business and industry, management's beliefs and certain assumptions made by
ARCA, all of which are subject to change. Such forward-looking statements are made as of the date of this release, and the parties undertake
no obligation to update such statements to reflect subsequent events or circumstances, except as otherwise required by securities and
other applicable law.
is not intended to and do not constitute (i) a solicitation of a proxy, consent or approval with respect to any securities or in
respect of the proposed transactions (the "Proposed Transactions") between ARCA and Oruka or (ii) an offer to
sell or the solicitation of an offer to subscribe for or buy or an invitation to purchase or subscribe for any securities pursuant to
the Proposed Transactions or otherwise, nor shall there be any sale, issuance or transfer of securities in any jurisdiction in contravention
of applicable law. No offer of securities shall be made except by means of a prospectus meeting the requirements of the Securities Act
of 1933, as amended, or an exemption therefrom. Subject to certain exceptions to be approved by the relevant regulators or certain facts
to be ascertained, the public offer will not be made directly or indirectly, in or into any jurisdiction where to do so would constitute
a violation of the laws of such jurisdiction, or by use of the mails or by any means or instrumentality (including without limitation,
facsimile transmission, telephone and the internet) of interstate or foreign commerce, or any facility of a national securities exchange,
of any such jurisdiction.

Frequently Asked Questions

What is ARCA's reverse stock split ratio?

ARCA's reverse stock split ratio is 1-for-12.

When will ARCA start trading under the name Oruka?

Trading as Oruka Therapeutics will begin on September 3, 2024.

How many shares will ARCA have after the split?

Post-split, ARCA will have approximately 1,208,928 outstanding shares.

What will happen to fractional shares after the split?

Stockholders will receive cash payments for any fractional shares.

What is Oruka Therapeutics focused on?

Oruka Therapeutics develops biologics for chronic skin diseases, including psoriasis.

Last updated: Aug 23, 2024