NEW YORK, July 16, 2018 (GLOBE NEWSWIRE) -- SELLAS Life Sciences Group, Inc. (NASDAQ:SLS) (“SELLAS” or the
“Company”), a clinical-stage biopharmaceutical company focused on the development of novel cancer immunotherapies for a broad range
of cancer indications, today announced the closing of its previously announced underwritten public offering of 6,845,000 shares of
common stock, 4,675,000 pre-funded warrants exercisable for shares of common stock, and accompanying common stock warrants to
purchase an aggregate of 11,520,000 shares of common stock. At closing, SELLAS received aggregate net proceeds from the offering of
approximately $21.6 million, after deducting underwriting discounts and commissions and estimated offering expense.
SELLAS intends to use the net proceeds from the offering to commence a pivotal Phase 3 trial of GPS in acute myeloid leukemia
(AML), and to develop GPS in combination with pembrolizumab (Keytruda) in a Phase 1/2 proof of concept study, as well as for
general corporate purposes and funding its working capital needs.
Cantor Fitzgerald & Co. and Oppenheimer & Co. Inc. acted as joint book-running managers for the offering. Maxim Group LLC acted
as lead manager.
A registration statement on Form S-1 relating to the offering was filed with the Securities and Exchange Commission (the "SEC")
on May 23, 2018, amended on June 26, 2018 and July 11, 2018 and was declared effective on July 11, 2018. The offering was made only
by means of a prospectus. SELLAS’ SEC filings are available to the public from the SEC's website at www.sec.gov. Copies of the final prospectus relating to the offering may also be obtained by
contacting Cantor Fitzgerald & Co., Attention: Equity Capital Markets, 499 Park Avenue, 6th Floor New York, New York 10022 or by
email at prospectus@cantor.com or Oppenheimer & Co. Inc., Attention: Equity Capital Markets, 85 Broad
Street, 26th Floor, New York, NY 10004 or by email at EquityProspectus@opco.com.
This press release shall not constitute an offer to sell or the 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.
About SELLAS
SELLAS is a clinical-stage biopharmaceutical company focused on novel cancer immunotherapeutics for a broad range of cancer
indications. SELLAS’ lead product candidate, galinpepimut-S (GPS), is licensed from Memorial Sloan Kettering Cancer Center and
targets the Wilms Tumor 1 (WT1) protein, which is present in an array of tumor types. GPS has potential as a monotherapy or in
combination to address a broad spectrum of hematologic malignancies and solid tumor indications. SELLAS has Phase 3 clinical trials
planned (pending funding availability) for GPS in two indications, acute myeloid leukemia (AML) and malignant pleural mesothelioma
(MPM) and is also developing GPS as a potential treatment for multiple myeloma (MM) and ovarian cancer. SELLAS plans to study GPS
in up to four additional indications. SELLAS has received Orphan Drug designations for GPS from the U.S. Food & Drug Administration
(FDA) for AML, MPM, and MM, as well as from the European Medicines Agency, for AML and MPM; GPS also received Fast Track
designation for AML and MPM from the FDA. SELLAS’ second product candidate, NeuVax™ (nelipepimut-S), is a HER2-directed cancer
immunotherapy being investigated for the prevention of the recurrence of breast cancer after standard of care treatment in the
adjuvant setting. NeuVax™ has received Fast Track status designation by FDA for the treatment of patients with early stage breast
cancer with low to intermediate HER2 expression, otherwise known as HER2 1+ or 2+, following standard of care.
Forward-Looking Statements
This press release contains forward-looking statements, including, but not limited to, statements related to SELLAS’ future
expectations, plans and prospects. These forward-looking statements are based on current plans, objectives, estimates, expectations
and intentions, and inherently involve significant risks and uncertainties. Actual results and the timing of events could differ
materially from those anticipated in such forward-looking statements as a result of these risks and uncertainties, which include,
without limitation, risks and uncertainties associated with clinical trials. These risks and uncertainties are described more fully
in Amendment No. 2 to Registration Statement on Form S-1 filed with the SEC on July 11, 2018 and other filings with
the Securities and Exchange Commission. Other risks and uncertainties of which SELLAS is not currently aware may also affect
SELLAS’ forward-looking statements. The forward-looking statements herein are made only as of the date hereof. SELLAS undertakes no
obligation to update or supplement any forward-looking statements to reflect actual results, new information, future events,
changes in its expectations or other circumstances that exist after the date as of which the forward-looking statements were
made.
Investor Contact:
Will O’Connor
Stern Investor Relations, Inc.
212-362-1200
ir@sellaslife.com
David Moser, JD
Sellas Life Sciences Group
813-864-2571
info@sellaslife.com
