Full Press Release Details
ADMA Biologics Reports Successful Close-Out
of its April 2018 FDA Compliance Inspection
FDA Establishment Inspection Report ("EIR")
RAMSEY, N.J. and BOCA RATON, FL., - July 26,
2018 - ADMA Biologics, Inc. (NASDAQ: ADMA) ("ADMA" or the "Company"), a vertically
integrated commercial biopharmaceutical company that manufactures, markets and develops specialty plasma-based biologics for
the prevention and treatment of certain infectious diseases, announces that the Company has received formal notice from the
U.S. Food and Drug Administration (the "FDA" or the "Agency") of the successful close-out for the
April 2018 compliance inspection of the Boca Raton, FL production facility. This is the first EIR issued to the site since
The EIR received by the Company contains detailed information
about the April 2018 FDA inspection, discussions had with the investigators, requests for clarification and information, as well
as a summary of potential next steps for the review of the Prior Approval Supplement ("PAS") for BIVIGAM . According
to FDA guidance, when the Agency concludes that an inspection is "closed" under 21 CFR 20.64(d) (3), it releases a
copy of the EIR to the inspected establishment.
The EIR discusses many improvements and resolutions made by
the Company to the majority of observations previously existing from the 2014 and 2016 FDA inspections of the Boca Raton, FL facility
while owned and operated by Biotest Pharmaceuticals Corporation ("Biotest"). The Agency has requested specific clarification
to certain historical inspectional deficiencies (from 2014 and 2016), some of which, the Company believes, will be addressed during
the ongoing review of the PAS for BIVIGAM . The EIR states that the FDA investigators were unable to review real time production
of BIVIGAM during the inspection and the report notes that the PAS had not yet been on file at the time of the April 2018
inspection. The Company believes that in order for FDA to make a final determination regarding the 2014 Warning Letter Close-Out,
a review of the PAS submission for BIVIGAM as well as a potential Pre-Approval Inspection ("PAI") of the manufacturing
process may be required. Based on separate informal correspondence received between the Company and FDA staff within the Center
for Biologics Evaluation and Research ("CBER"), the Company has been informed that its compliance status is currently
Voluntary Action Indicated ("VAI"), which remains to be confirmed with CBER's Office of Compliance and Biologics
Quality ("OCBQ"). In addition, the FDA has stated to the Company that the 483 responses have been reviewed and corrective
actions will be assessed at the next FDA inspection of the establishment, which is anticipated by the Company to occur on or before
the end of April 2020.
The Company's assessment of the information received by
FDA results in the following determinations:
"We are pleased that the FDA has determined our responses
to be satisfactory for the April 2018 FDA compliance inspection and that the FDA has accepted our plan for remediation to their
observations and closed this inspection. We believe that we have successfully remediated the production and significant compliance
issues identified in the 2014 Warning Letter and subsequent 2016 cGMP inspection issued to Biotest as evidenced by the successful
production of three conformance batches for BIVIGAM , which were the basis for our June 2018 PAS submission. Furthermore, we
believe that once the FDA has reviewed the PAS and performed an inspection of the manufacturing operations for BIVIGAM , we
will be in position to relaunch BIVIGAM in the U.S. and further improve our compliance status," stated Adam Grossman, President
and Chief Executive Officer of ADMA Biologics, Inc.
Mr. Grossman further stated, "We are thankful for the
extraordinary efforts of our dedicated and hard-working employees who have been relentlessly committed to improving the Company's
FDA compliance status."
The receipt of this EIR does not change the Company's
previously reported timelines for activities, regulatory submissions and approvals. The Company remains on target to have the BIVIGAM
PAS approved and the BLA for RI-002 refiled with the FDA during the second half of 2018.
ADMA Biologics, Inc. (ADMA)
ADMA Biologics is a vertically integrated commercial biopharmaceutical company that manufactures, markets and develops specialty
plasma-based biologics for the treatment of Primary Immune Deficiency Disease ("PIDD") and the prevention and treatment
of certain infectious diseases. ADMA's mission is to develop and commercialize plasma-derived, human immune globulins targeted
to niche patient populations for the treatment and prevention of certain infectious diseases. The target patient populations include
immune-compromised individuals who suffer from an underlying immune deficiency disease, or who may be immune-compromised for other
medical reasons. ADMA has received U.S. Patents 9,107,906, 9,714,283, 9,815,886 and 9,969,793 related to certain aspects of its
lead product candidate, RI-002. For more information, please visit www.admabiologics.com.
BIVIGAM is an intravenous immune globulin indicated for
the treatment of primary humoral immunodeficiency. This includes, but is not limited to, agammaglobulinemia, common variable immunodeficiency,
Wiskott-Aldrich syndrome and severe combined immunodeficiency. These primary immunodeficiencies ("PI") are a group
of genetic disorders. Initially thought to be very rare, it is now believed that as many as 250,000 people in the U.S. have some
form of PI. BIVIGAM contains a broad range of antibodies similar to those found in normal human plasma. These antibodies are
directed against bacteria and viruses, and help to protect PIDD patients against serious infections. BIVIGAM is a purified,
sterile, ready-to-use preparation of concentrated polyclonal Immunoglobulin ("IgG") antibodies. Antibodies are proteins
in the human immune system that work to defend against infections and disease. FDA approval for BIVIGAM was received by Biotest
Pharmaceuticals Corporation ("BPC" or "Biotest") on December 19, 2012, and production of BIVIGAM was
halted by Biotest in December 2016. ADMA Biologics obtained ownership and all rights, title and interest in BIVIGAM on June
6, 2017 as part of the Biotest Therapy Business Unit ("BTBU") asset acquisition. ADMA optimized the production process
for BIVIGAM and submitted a Prior Approval Supplement ("PAS") to the United States Food and Drug Administration
("FDA") to amend the Biologics License Application ("BLA") for BIVIGAM in June of 2018, with a target
action date of October 25, 2018 under the Prescription Drug User Fee Act ("PDUFA"). If the PAS is approved by the FDA,
ADMA expects to be able to relaunch the product for commercial sale by the end of the first quarter of 2019.
ADMA's lead portfolio product candidate, RI-002, which has demonstrated positive Phase III pivotal clinical trial data, is a specialty
plasma-derived, polyclonal, intravenous immune globulin ("IVIG") derived from human plasma containing naturally occurring
polyclonal antibodies (e.g., Streptococcus pneumoniae, H. influenza type B, cytomegalovirus ("CMV"), measles, tetanus,
etc.) as well as plasma from donors tested to have high levels of neutralizing antibodies to respiratory syncytial virus ("RSV").
ADMA is pursuing an indication for the use of this specialty IVIG product for treatment of patients diagnosed with PIDD. Polyclonal
antibodies are the primary active component of IVIG products. Polyclonal antibodies are proteins that are used by the body's immune
system to neutralize microbes, such as bacteria and viruses and prevent against infection and disease. Data review which has been
published in peer reviewed journals indicates that the polyclonal antibodies present in RI-002 support its ability to prevent infections
in immune-compromised patients. This data and other information about RI-002 or ADMA Biologics products can be found on the Company
website at: www.admabiologics.com/therapies and www.admabiologics.com. RI-002 is protected by U.S. Patents: 9,107,906, 9,714,283,
9,815,886 and 9,969,793, the latter of which affords the Company patent exclusivity for the use of an immune globulin as a prevention
and/or treatment for any type of respiratory infection.
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 the words "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 also include, but are not limited to, statements concerning our plans to develop,
manufacture, market, launch and expand our own commercial infrastructure and commercialize our current products and future products,
the safety, efficacy and expected timing of, and our ability to, obtain and maintain regulatory approvals of our current products
and product candidates, and the labeling or nature of any such approvals, the success of our work with our third party vendors
and the U.S. Food and Drug Administration (the "FDA") in furtherance of and progress towards an approval of our Biologics
License Application for specialty plasma-based biologics and the ability of such third parties to respond adequately or in a timely
manner to the issues raised by the FDA, our ability to successfully pursue commercialization and prelaunch activities, the timeframe
within which we may receive approval from the FDA for specialty plasma-based biologics, if at all, the potential of our specialty
plasma-based biologics to provide meaningful clinical improvement for patients living with Primary Immune Deficiency Disease or
other indications, our ability to realize increased prices for plasma growth in the plasma collection industry and our expectations
for future capital requirements. Actual events or results may differ materially from those described in this document 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. In light of the significant uncertainties