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RAMSEY, N.J. and BOCA RATON, Fla., Aug 05, 2020 (GLOBE NEWSWIRE via COMTEX) — Generated Total Revenues of $18.0 Actor for the Aboriginal Bisected of 2020, Reflecting a 78% Admission Over Aboriginal Bisected of 2019

Joined CoVIg-19 Claret Alliance and Auspiciously Opened New ADMA BioCenters Claret Accumulating Center



Company Anticipates Breeding $250 Actor or Added in Anniversary Revenues Aural Abutting Three to Bristles Agenda Years



Management to Host Appointment Alarm and Webcast Today at 4:30 p.m. ET

RAMSEY, N.J. and BOCA RATON, Fla., Aug. 05, 2020 (GLOBE NEWSWIRE) — ADMA Biologics, Inc. (Nasdaq: ADMA) (“ADMA”), an end-to-end bartering biopharmaceutical aggregation committed to manufacturing, business and developing specialty plasma-derived biologics, today appear business highlights and banking after-effects for its budgetary added division and six months assured June 30, 2020, and provided an overview of contempo advance and accomplishments.

“The aboriginal bisected of 2020 was apparent by several achievements and challenges as we cross through these aberrant macro-market conditions,” said Adam Grossman, President and Chief Executive Officer of ADMA. “Total revenues for the aboriginal bisected of 2020 added about 78% compared to the aforementioned above-mentioned year period. While the added division 2020 revenues were about 19% college than added division 2019 revenues, ADMA, and assertive of its third-party vendors, accomplished impacts from the all-around COVID-19 communicable which resulted in abrupt accumulation alternation disruptions. These COVID-19 disruptions were primarily accompanying to delays with final artefact Accepted Acceptable Accomplishment Practice (“cGMP”) absolution testing by third-party vendors. This agency that a few of our assembly batches were accomplished on agenda but we were clumsy to abide for U.S. Food and Drug Administration (“FDA”) lot absolution allotment due to delayed analysis results.

“These delays were mainly accomplished during the closing allotment of the added division and accept back been bound during July. In acknowledgment to these delays, and in affiliation with the FDA, we added added absolution testing laboratories to our accustomed bunch and accept we accept absolutely bound the affair and do not ahead added testing or accumulation absolution delays activity forward.

“Market appeal for our immunoglobulin artefact portfolio charcoal able and we ahead ample acquirement advance for the added bisected of the year and are aflame for the advancing assembly aggregate increases from our accommodation amplification efforts in 2021 and beyond. We additionally accept we abide on clue to accomplish our declared ambition of breeding $250 actor or added in anniversary revenues aural the abutting three to bristles agenda years.

“In accordance with our declared accumulated objectives, during the division we completed architecture of a new claret accumulating center, accomplished donor collections and submitted a Biologics License Appliance (“BLA”) to the FDA, with an approval accommodation accepted in mid-2021. We additionally installed and able a new antibacterial fill-finish apparatus at our Boca Raton facility, and bogus acclimation batches of BIVIGAM(R) at an added calibration that will ultimately acquiesce us to accomplish at alert the aggregate as the action that is in abode today. And finally, we abutting the CoVIg-19 Claret Alliance and began accumulating of claret from COVID-19 convalesced patients. We are appreciative of these important achievements and milestones and accept we accept set the date to now be in a position to ensure the U.S. bazaar has a connected accumulation of BIVIGAM(R), ASCENIV(TM) and NABI-HB(R). We are on ambition for accession our operations to capitalize on the connected forecasted advance of the claret articles industry. Our assembly throughput and accomplished artefact accumulation charcoal on clue to activate acumen the allowances from these initiatives as aboriginal as mid-2021,” assured Mr. Grossman.

Second Division 2020 Highlights and Contempo Events

COVID-19 Impacts

Financial After-effects for the Three Months Assured June 30, 2020

Total revenues for the division assured June 30, 2020 were $7.8 million, compared to $6.6 actor for the division assured June 30, 2019, apery an admission of about $1.2 million, or about 19%. The admission is primarily due to sales of BIVIGAM, ASCENIV and intermediates, compared to no sales from these articles during the aforementioned above-mentioned year period. ADMA’s revenues for the added division of 2020, compared to the added division of 2019, were agreeably impacted by the FDA approvals of BIVIGAM and ASCENIV on May 9, 2019 and April 1, 2019, respectively, and by the accomplishment and accumulation acceding ADMA entered into in January 2020 to aftermath and advertise average fractions to a assertive customer.

Consolidated net accident for the division assured June 30, 2020 was $20.2 million, or $(0.23) per basal and adulterated share, compared to a circumscribed net accident of $13.2 million, or $(0.25) per basal and adulterated share, for the division assured June 30, 2019. The admission in net accident of $7.0 actor was primarily due to added amount of artefact acquirement of $3.0 actor accompanying to sales of FDA-approved immunoglobulin articles not present in the aforementioned above-mentioned year period, forth with the absolute costs associated with the accomplishment of BIVIGAM’s added claret basin acclimation lots as allotment of our planned accommodation expansion, partially account by a abatement in unabsorbed accomplishment amount at the Boca Raton, FL assembly facility. The admission in net accident during the added division of 2020 is additionally attributable to college analysis and development costs of $1.1 million, abundantly due to costs associated with the testing and development of a new bushing band at one of our third-party ample finishers, and to added selling, accepted and authoritative costs of $2.6 million, mainly due to increases in agent advantage costs and added costs in abutment of our commercialization efforts for BIVIGAM and ASCENIV. In addition, absorption amount for the division added by $1.0 actor due to our accessing added debt during the added division of 2019 and aboriginal division of 2020. Included in the net accident for the added division of 2020 were non-cash costs of about $2.0 actor for stock-based compensation, abrasion and amortization, and non-cash absorption expense.

Financial After-effects for the Six Months Assured June 30, 2020

Total revenues for the six months assured June 30, 2020 were $18.0 million, compared to $10.1 actor for the six months assured June 30, 2019, apery an admission of $7.9 million, or about 78%. The admission in revenues was primarily attributable to sales of BIVIGAM, ASCENIV and intermediates, compared to no sales from these articles during the aforementioned above-mentioned year period.

Consolidated net accident for the six months assured June 30, 2020 was $39.4 million, or $(0.49) per basal and adulterated share, compared to a circumscribed net accident of $26.3 million, or $(0.53) per basal and adulterated share, for the six months assured June 30, 2019. The admission in net accident of $13.1 actor was primarily attributable to added amount of artefact acquirement of $10.4 actor accompanying to sales of BIVIGAM, ASCENIV and intermediates not present during the aboriginal bisected of 2019, forth with the costs associated with the accomplishment of BIVIGAM’s added claret basin acclimation lots as allotment of our planned accommodation expansion, forth with added assembly initiatives and investments at the Boca Raton facility. Added factors accidental to the admission in net accident include: college analysis and development costs attributed to costs associated with testing and development of a new ample band at our third-party ample finisher and costs incurred for a abstraction we commenced to potentially extend ASCENIV’s accustomed and labeled cessation dating, college selling, accepted authoritative costs in abutment of our commercialization efforts of BIVIGAM’s relaunch and ASCENIV’s barrage and the all-embracing advance in the admeasurement and ambit of the Company’s operations forth with college absorption amount due to accessing added debt during the added division of 2019 and aboriginal division of 2020. Included in the net accident for the aboriginal bisected of 2020 were non-cash costs of about $3.9 actor for stock-based compensation, abrasion and amortization, and non-cash absorption expense.

At June 30, 2020, ADMA had banknote and banknote equivalents of $75.8 actor and accounts receivable of $6.5 million, compared to banknote and banknote equivalents of $26.8 actor and accounts receivable of $3.5 actor at December 31, 2019. ADMA’s net alive basic as of June 30, 2020 was $130.1 million, compared to $71.8 actor as of December 31, 2019.

Conference Alarm Information

ADMA will host a appointment alarm today, Wednesday, August 5, 2020, at 4:30 p.m. Eastern Time, to altercate the added division 2020 banking after-effects and contempo accumulated updates. To admission the appointment call, amuse punch (855) 884-8773 (local) or (615) 622-8043 (international) at atomic 10 account above-mentioned to the alpha time and accredit to appointment ID 8992308. A alive audio webcast of the alarm will be accessible beneath “Events & Webcasts” in the Investor area of the Company’s website, https://ir.admabiologics.com/events-webcasts. An archived webcast will be accessible on the Company’s website about two hours afterwards the event.

About BIVIGAM(R)

BIVIGAM (immune globulin intravenous, animal – 10% liquid) is a plasma-derived, polyclonal, intravenous allowed globulin (IVIG). BIVIGAM was accustomed by the FDA in May 2019 and is adumbrated for the analysis of primary humoral immunodeficiency (PI), including, but not bound to the afterward accumulation of abiogenetic disorders: X-linked and complete agammaglobulinemia, accepted capricious immunodeficiency, Wiskott-Aldrich affection and astringent accumulated immunodeficiency. BIVIGAM contains a ample ambit of antibodies agnate to those begin in accustomed animal plasma. These antibodies are directed adjoin bacilli and bacilli and advice to assure PI patients adjoin austere infections. BIVIGAM is a purified, sterile, ready-to-use alertness of concentrated animal Immunoglobulin (IgG) antibodies.

About ASCENIV(TM)

ASCENIV (immune globulin intravenous, animal – slra 10% liquid) is a plasma-derived, polyclonal, intravenous allowed globulin (IVIG). ASCENIV was accustomed by the FDA on April 1, 2019 and is adumbrated for the analysis of primary humoral immunodeficiency (PI), additionally accepted as primary allowed absence ache (PIDD), in adults and adolescents (12 to 17 years of age). ASCENIV is bogus appliance ADMA’s unique, patented claret donor screening alignment and tailored claret pooling design, which blends accustomed antecedent claret and claret from donors activated appliance the Company’s proprietary microneutralization assay. ASCENIV contains artlessly occurring polyclonal antibodies, which are proteins that are acclimated by the body’s allowed arrangement to abrogate microbes, such as bacilli and bacilli and anticipate adjoin infection and disease. ASCENIV is adequate by U.S. Patents: 9,107,906, 9,714,283 and 9,815,886.

About Nabi-HB(R)

Nabi-HB(R) is a hyperimmune globulin that is affluent in antibodies to the Hepatitis B virus. Nabi-HB(R) is a antiseptic animal polyclonal antibiotic artefact calm from claret donors who accept been ahead vaccinated with a Hepatitis B vaccine. Nabi-HB(R) is adumbrated for the analysis of astute acknowledgment to claret absolute Hepatitis B apparent antigen (“HBsAg”), prenatal acknowledgment to breed built-in to HBsAg-positive mothers, animal acknowledgment to HBsAg-positive bodies and domiciliary acknowledgment to bodies with astute Hepatitis B virus infection. Hepatitis B is a potentially life-threatening alarmist infection acquired by the Hepatitis B virus. It is a above all-around bloom botheration and can account abiding infection and put bodies at aerial accident of afterlife from cirrhosis and alarmist cancer. Nabi-HB(R) has a well-documented almanac of abiding affirmation and capability back its antecedent bazaar introduction. Assertive abstracts and added advice about Nabi-HB(R) or ADMA Biologics and its articles can be begin on the Company’s website at www.admabiologics.com.

About ADMA BioCenters

ADMA BioCenters is an FDA accountant adeptness specializing in the accumulating of animal claret acclimated to accomplish adapted medications for the analysis and blockage of diseases. Managed by a aggregation of experts who accept decades of acquaintance in the specialized acreage of claret collection, ADMA BioCenters provides a safe, able and affable donation environment. ADMA BioCenters carefully follows FDA regulations and advice and enforces cGMP (current acceptable accomplishment practices) in all of its facilities. For added advice about ADMA BioCenters, amuse appointment www.atlantaplasma.com.

About ADMA Biologics, Inc. (ADMA)

ADMA Biologics is an end-to-end bartering biopharmaceutical aggregation committed to manufacturing, business and developing specialty plasma-derived biologics for the analysis of immunodeficient patients at accident for infection and others at accident for assertive communicable diseases. ADMA currently articles and markets three United States Food and Drug Administration (FDA) accustomed plasma-derived biologics for the analysis of allowed deficiencies and the blockage of assertive communicable diseases: ASCENIV(TM) (immune globulin intravenous, animal – slra 10% liquid) for the analysis of primary humoral immunodeficiency (PI); BIVIGAM(R) (immune globulin intravenous, human) for the analysis of PI; and NABI-HB(R) (hepatitis B allowed globulin, human) to accommodate added amnesty adjoin the hepatitis B virus. ADMA articles its allowed globulin articles at its FDA-licensed claret fractionation and ablution adeptness amid in Boca Raton, Florida. Through its ADMA Bio Centers subsidiary, ADMA additionally operates as an FDA-approved antecedent claret beneficiary in the U.S., which provides a allocation of its claret claret for the accomplish of its products. ADMA’s mission is to manufacture, bazaar and advance specialty plasma-derived, animal allowed globulins targeted to alcove accommodating populations for the analysis and blockage of assertive communicable diseases and administration of allowed compromised accommodating populations who ache from an basal allowed deficiency, or who may be allowed compromised for added medical reasons. ADMA has accustomed U.S. Patents: 9,107,906, 9,714,283, 9,815,886, 9,969,793 and 10,259,865 accompanying to assertive aspects of its articles and artefact candidates. For added information, amuse appointment www.admabiologics.com.

Cautionary Agenda Regarding Forward-Looking Statements

This columnist absolution contains “forward-looking statements” pursuant to the safe anchorage accoutrement of the Private Securities Litigation Reform Act of 1995, about ADMA Biologics, Inc. (“we,” “our” or the “Company”). Advanced statements include, after limitation, any account that may predict, forecast, indicate, or betoken approaching results, achievement or achievements, and may accommodate such words as “estimate,” “project,” “intend,” “forecast,” “target,” “anticipate,” “plan,” “planning,” “expect,” “believe,” “will,” “should,” “could,” “would,” “may,” or, in anniversary case, their negative, or words or expressions of agnate meaning. These advanced statements additionally include, but are not bound to, statements about ADMA’s approaching after-effects of operations, including the ambition of breeding $250 actor or added in anniversary revenues aural the abutting three to bristles agenda years; our acceptance that we accept adapted third-party absolution testing adjournment issues through the accession of absolution testing laboratories to our FDA-approved consortium; the aftereffect and timing of our BLA appliance for our new claret center; the accepted allowances from the new antibacterial fill-finish apparatus installed at our Boca Raton facility; the connected forecasted advance of the claret articles industry and our apprehension to capitalize thereon; the architecture and aperture of claret accumulating centers and the timing thereof; the accepted and advised use by the CoVIg-19 Claret Alliance of claret that we collect; the allowances accepted from our several accomplishment and accumulation alternation enhancement, the accepted timing for acumen those benefits, and our plan to abide adapted applications to the FDA accompanying thereto; and the accepted allowances from accepting added third-party laboratories to accomplish cGMP absolution testing. Absolute contest or after-effects may alter materially from those declared in this certificate due to a cardinal of important factors. Accepted and -to-be aegis holders are cautioned that there additionally can be no affirmation that the advanced statements included in this columnist absolution will prove to be accurate. Except to the admeasurement appropriate by applicative laws or rules, ADMA does not undertake any obligation to amend any advanced statements or to advertise revisions to any of the advanced statements. Advanced statements are accountable to abounding risks, uncertainties and added factors that could account our absolute results, and the timing of assertive events, to alter materially from any approaching after-effects bidding or adumbrated by the advanced statements, including, but not bound to, the risks and uncertainties declared in our filings with the U.S. Securities and Exchange Commission, including our best contempo letters on Form 10-K, 10-Q and 8-K, and any amendments thereto.

COMPANY CONTACT:

Brian Lenz

Executive Vice President and Chief Banking Officer | 201-478-5552 |www.admabiologics.com

INVESTOR RELATIONS CONTACT:

Sam Martin

Managing Director, Argot Partners | 212-600-1902 | [email protected]

ADMA BIOLOGICS, INC. AND SUBSIDIARIESCONSOLIDATED STATEMENTS OF OPERATIONS

ADMA BIOLOGICS, INC. AND SUBSIDIARIESCONDENSED CONSOLIDATED BALANCE SHEETS

COMTEX_368950655/2471/2020-08-05T23:02:42

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The MarketWatch News Department was not complex in the conception of this content.

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