Recent Updates
Recently added Catalysts
ENLV

Enlivex Announces Closing of Previously Announced Bought Deal Offering of Approximately $46.0 Million Ordinary Shares Nes Ziona, Israel

Key Takeaway: Enlivex Announces Closing of Previously Announced Bought Offering of Approximately $46.0 Million Ordinary Shares Feb. 12, 2021, Enlivex Therapeutics Ltd. (NASDAQ: ENLV), a clinical-stage macrophage reprogramming immunotherapy company targeting diseased macrophages in patients

Full Press Release Details

Enlivex Announces Closing of Previously Announced Bought
Offering of Approximately $46.0 Million Ordinary Shares
Feb. 12, 2021, Enlivex Therapeutics Ltd. (NASDAQ: ENLV), a clinical-stage macrophage reprogramming immunotherapy company
targeting diseased macrophages in patients with sepsis, COVID-19 and solid tumors, today announced the closing of its previously
announced offering of 2,296,107 ordinary shares, par value NIS 0.40 per share, of the Company at a price to the public of $20.00
per ordinary share, less underwriting discounts and commissions.
Co. acted as the sole book-running manager for the offering.
The Company also has
granted to the underwriter a 30-day option to purchase up to 344,416 additional ordinary shares at the public offering price, less
underwriting discounts and commissions.
to Enlivex, before deducting underwriting discounts and commissions and offering expenses, are approximately $45.92 million. The
Company intends to use the net proceeds from this offering for (i) clinical, regulatory, manufacturing and research and development
activities; (ii) potential acquisitions and in-licensing; and (iii) other general corporate purposes.
The securities described
above were offered by Enlivex pursuant to a "shelf" registration statement on Form F-3 (File No. 333-232009) previously
filed with the Securities and Exchange Commission (the "SEC") on June 7, 2019 and declared effective by the SEC on
June 21, 2019 and the Form F-3MEF filed on February 9, 2021 (File No. 333-252926). The offering of the securities described above
was made only by means of a prospectus, including a prospectus supplement, forming a part of the effective registration statement.
A final prospectus supplement and accompanying prospectus relating to the securities offered have been filed with the SEC and are
available on the SEC's website at http://www.sec.gov or by contacting H.C. Wainwright & Co., LLC at 430 Park
Avenue, 3rd Floor, New York, NY 10022, by phone at (646) 975-6996 or e-mail at placements@hcwco.com.
shall not constitute an offer to sell or a solicitation of an offer to buy these securities, nor shall there be any sale of these
securities in any state or other jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration
or qualification under the securities laws of any such state or other jurisdiction.
is a clinical stage macrophage reprogramming immunotherapy company developing AllocetraTM, a universal, off-the-shelf
cell therapy designed to reprogram macrophages into their homeostatic state. Resetting non-homeostatic macrophages into their
homeostatic state is critical for immune system rebalancing and resolution of life-threatening conditions. For more information,
Safe Harbor Statement:
This press release contains forward-looking statements, which may be identified by words such as "expects," "plans,"
"projects," "will," "may," "anticipates," "believes," "should,"
"would", "could," "intends," "estimates," "suggests," "has the
potential to" and other words of similar meaning, including statements regarding expected cash balances, market opportunities
for the results of current clinical studies and preclinical experiments, the effectiveness of, market opportunities for, ALLOCETRATM programs,
and statements relating to the bought deal offering, including as to the intended use of proceeds. All such forward-looking statements
are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Investors are cautioned
that forward-looking statements involve risks and uncertainties that may affect Enlivex's business and prospects, including
market and other conditions and the risks that Enlivex may not succeed in generating any revenues or developing any commercial
products; that the products in development may fail, may not achieve the expected results or effectiveness and/or may not generate
data that would support the approval or marketing of these products for the indications being studied or for other indications;
that ongoing studies may not continue to show substantial or any activity; and other risks and uncertainties that may cause results
to differ materially from those set forth in the forward-looking statements. The results of clinical trials in humans may produce
results that differ significantly from the results of clinical and other trials in animals. The results of early-stage trials may
differ significantly from the results of more developed, later-stage trials. The development of any products using the ALLOCETRATM product
line could also be affected by a number of other factors, including unexpected safety, efficacy or manufacturing issues, additional
time requirements for data analyses and decision making, the impact of pharmaceutical industry regulation, the impact of competitive
products and pricing and the impact of patents and other proprietary rights held by competitors and other third parties.
In addition to the risk factors described above, investors should consider the economic, competitive, governmental, technological
and other factors discussed in Enlivex's filings with the Securities and Exchange Commission, including in the Company's
most recent Annual Report on Form 20-F filed with the Securities and Exchange Commission. The forward-looking statements
contained in this press release speak only as of the date the statements were made, and we do not undertake any obligation to update
forward-looking statements, except as required under applicable law.
Shachar Shlosberger,
Enlivex Therapeutics,
Last updated: Feb 12, 2021