ADMA Biologics Announces Partial Paydown of Senior Term Loan Credit Facility
December 20 2024 - 7:00AM
ADMA Biologics, Inc. (Nasdaq: ADMA) (“ADMA” or the “Company”), an
end-to-end commercial biopharmaceutical company dedicated to
manufacturing, marketing and developing specialty biologics, today
announced it has repaid $30 million from its original $62.5 million
senior secured term loan facility with Ares Capital. Following the
partial paydown, ADMA has further reduced its total gross debt to
$75 million, comprised of its $42.5 million revolving credit
facility and $32.5 million now outstanding under its term loan
credit facility. The partial paydown was funded by utilizing cash
on hand.
"ADMA’s organically generated cash flow has
enabled the pay down of $30 million of our senior secured credit
facility,” said Adam Grossman, President and Chief Executive
Officer of ADMA. “The second paydown of our senior credit facility
in four months reduces our total gross debt by 29%, and the lowered
interest expense is expected to further enhance our earnings growth
potential in the immediate periods ahead. This decision is a
testament to our confidence in the sustained growth of earnings and
the anticipated ongoing cash generation. We expect to further
reduce and optimize ADMA’s cost of both debt and equity capital
going forward.”
About ADMA Biologics, Inc.
(ADMA)
ADMA Biologics is an end-to-end commercial
biopharmaceutical company dedicated to manufacturing, marketing and
developing specialty biologics for the treatment of immunodeficient
patients at risk for infection and others at risk for certain
infectious diseases. ADMA currently manufactures and markets three
United States Food and Drug Administration (FDA)-approved
plasma-derived biologics for the treatment of immune deficiencies
and the prevention of certain infectious diseases: BIVIGAM® (immune
globulin intravenous, human) for the treatment of primary humoral
immunodeficiency (PI); ASCENIV™ (immune globulin intravenous, human
– slra 10% liquid) for the treatment of PI; and NABI-HB® (hepatitis
B immune globulin, human) to provide enhanced immunity against the
hepatitis B virus. ADMA manufactures its immune globulin products
at its FDA-licensed plasma fractionation and purification facility
located in Boca Raton, Florida. Through its ADMA BioCenters
subsidiary, ADMA also operates as an FDA-approved source plasma
collector in the U.S., which provides its blood plasma for the
manufacture of its products. ADMA’s mission is to manufacture,
market and develop specialty biologics and human immune globulins
targeted to niche patient populations for the treatment and
prevention of certain infectious diseases and management of immune
compromised patient populations who suffer from an underlying
immune deficiency, or who may be immune compromised for other
medical reasons. ADMA holds numerous U.S. and foreign patents
related to and encompassing various aspects of its products and
product candidates. For more information, please visit
www.admabiologics.com.
Cautionary Note Regarding
Forward-Looking Statements
This press release contains “forward-looking
statements” pursuant to the safe harbor provisions of the Private
Securities Litigation Reform Act of 1995, about ADMA Biologics,
Inc. (“we,” “our” or the “Company”). Forward-looking statements
include, without limitation, any statement that may predict,
forecast, indicate, or imply future results, performance or
achievements, and may contain such words as “confident,”
“estimate,” “project,” “intend,” “forecast,” “target,”
“anticipate,” “plan,” “planning,” “expect,” “believe,” “will,” “is
likely,” “will likely,” “should,” “could,” “would,” “may,” or, in
each case, their negative, or words or expressions of similar
meaning. These forward-looking statements include, but are not
limited to, statements about the Company’s future results of
operations, including, but not limited to, the Company’s earnings
growth outlook, cash balance and cost of debt and equity capital,
as well as expected benefits from paying down outstanding debt.
Actual events or results may differ materially from those described
in this press release due to a number of important factors. Current
and prospective security holders are cautioned that there also can
be no assurance that the forward-looking statements included in
this press release will prove to be accurate. Except to the extent
required by applicable laws or rules, ADMA does not undertake any
obligation to update any forward-looking statements or to announce
revisions to any of the forward-looking statements. Forward-looking
statements are subject to many risks, uncertainties and other
factors that could cause our actual results, and the timing of
certain events, to differ materially from any future results
expressed or implied by the forward-looking statements, including,
but not limited to, the risks and uncertainties described in our
filings with the U.S. Securities and Exchange Commission, including
our most recent reports on Form 10-K, 10-Q and 8-K, and any
amendments thereto.
INVESTOR RELATIONS
CONTACT:Michelle Pappanastos Senior Managing Director,
Argot Partners | 212-600-1902 | michelle@argotpartners.com
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