ADMA Biologics Announces Partial Paydown of Revolving Credit Facility
14 Agosto 2024 - 2:59PM
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 $72.5 million
revolving credit facility with Ares Capital. Following the partial
paydown, ADMA has reduced its total gross debt to $105 million,
comprised of its existing $62.5 million term loan and $42.5 million
now outstanding under its revolving 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 revolving credit
facility,” said Adam Grossman, President and Chief Executive
Officer of ADMA. “The paydown reduces our total gross debt by 22%,
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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