RAMSEY, N.J., Aug. 11, 2017 (GLOBE NEWSWIRE) -- ADMA Biologics, Inc. (NASDAQ:ADMA) (“ADMA” or the “Company”), a vertically integrated biopharmaceutical and specialty immunoglobulin company that develops, manufactures and markets specialty plasma-based biologics for the treatment of Primary Immune Deficiency Disease (“PIDD”) and the prevention and treatment of certain infectious diseases, today announced its financial results for the quarter ended June 30, 2017 and provided a corporate update.
“We are very pleased with the Company’s transformative progress achieved during the second quarter of 2017. Most importantly, we successfully completed the acquisition of certain assets pertaining to the Biotest Pharmaceuticals Corporation Therapy Business Unit (“BTBU”), continued to integrate business operations, implemented certain departmental synergies and generated accretive revenues, which helped drive quarter-over-quarter sales growth by approximately 50%,” stated Adam Grossman, President and Chief Executive Officer of ADMA.
Mr. Grossman continued, “Also, during the second quarter of 2017, we engaged a leading consulting firm that manages a robust team of Subject Matter Experts (“SMEs”) with a focus on plasma derived products and biologics drugs, and which has extensive experience in remediating U.S. Food and Drug Administration (“FDA”) compliance and inspection matters. The role of this SME advisory firm is to assist and augment the Company’s resources in order to expeditiously resolve the inherited issues related to the acquired Boca Raton, FL Facility’s (the “Boca Facility”) quality management systems. Most recently, in July 2017 we were issued another patent attributable to RI-002, our lead pipeline product candidate, which encompasses methods of providing immunotherapy to patients using immune globulin compositions proprietary to ADMA, thus enhancing our intellectual proprietary portfolio and continuing to provide exclusivity until January 2035,” Mr. Grossman concluded.
2017 YTD Achievements and Anticipated Goals
- Consummated and closed the acquisition of the BTBU, making ADMA a vertically integrated manufacturer and provider of specialty immune globulin products
- Ongoing successful integration of BTBU operations into ADMA
- Established a timeline and engaged SMEs to assist with the remediation of the FDA warning letter for the acquired Boca Facility
- Set a corporate goal to be “Inspection Ready” by year end 2017
- Continue to generate and build on additional accretive revenues from FDA approved BTBU acquired assets
- Initiated the buildout of another ADMA BioCenter plasma collection facility
- Issued a second patent for immunotherapeutics methods for RI-002
Financial Results for the Three Months Ended June 30, 2017
ADMA reported revenues of $3.4 million for the second quarter ended June 30, 2017, compared to $2.3 million for the second quarter ended June 30, 2016, representing a quarter-over-quarter increase of approximately 50%. This growth was primarily attributable to sales generated from our second plasma center, as well as sales of Nabi-HB® as a result of our recent acquisition of certain BTBU assets, which include the commercial rights to Nabi-HB®.
The consolidated net loss for the quarter ended June 30, 2017 was $9.0 million, or $0.55 per basic and diluted share, as compared to a consolidated net loss of $6.0 million, or $0.50 per basic and diluted share, for the quarter ended June 30, 2016. The increase in net loss was primarily attributable to increased manufacturing costs, Boca Facility costs and third-party consultant fees pertaining to the remediation efforts in response to the FDA warning letter at the Boca Facility of $3.2 million. The increased net loss was also attributed to professional fees and other expenses incurred for the acquisition of the BTBU assets of $1.2 million. The increased net loss was partially offset by decreased research and development expenses of $2.0 million as a result of lower validation, testing and production costs related to RI-002 along with increased revenues from our plasma centers and sales of Nabi-HB®. Included in the net loss for the second quarter ended June 30, 2017 were non-cash expenses of $0.3 million for stock-based compensation and $0.2 million for depreciation and amortization.
Financial Results for the Six Months Ended June 30, 2017
ADMA reported revenues of $6.0 million for the six months ended June 30, 2017, as compared to $4.4 million for the six months ended June 30, 2016, representing an increase of 37%, which was a result of the continued growth in the plasma collection business and sales of Nabi-HB®.
The consolidated net loss for the six months ended June 30, 2017 was $15.6 million, or $1.06 per basic and diluted share, as compared to a consolidated net loss of $10.6 million, or $0.93 per basic and diluted share, for the six months ended June 30, 2016. The increase in net loss was primarily attributable to professional fees and other expenses incurred for the acquisition of the BTBU assets of $3.8 million and increased manufacturing costs and remediation consulting fees associated with the Boca Facility FDA warning letter, partially offset by decreased research and development expenses. Included in the net loss for the six months ended June 30, 2017 were non-cash expenses of $0.5 million for stock-based compensation and $0.4 million for depreciation and amortization.
At June 30, 2017, ADMA had cash and cash equivalents of $25.6 million, as compared to $15.3 million at December 31, 2016. ADMA’s net working capital as of June 30, 2017 was $28.6 million, as compared to $10.4 million as of December 31, 2016.
About ADMA Biologics, Inc. (ADMA)
ADMA is a vertically integrated biopharmaceutical and specialty immunoglobulin company that develops, manufactures and markets 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 medical reasons. ADMA has received U.S. Patents 9,107,906 and 9,714,283 related to certain aspects of its product candidate, RI-002. For more information, please visit www.admabiologics.com.
This press release contains "forward-looking statements" pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. 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," "intend," "target,” “will," “is likely,” "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 concerning our ability to develop, manufacture, and commercialize specialty plasma-based biologics for the proposed treatment of immune deficiencies and the prevention of certain infectious diseases, the success of our work with our third party vendors and the U.S. Food and Drug Administration 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 PIDD or other indications and our ability to realize increased prices for plasma growth in the plasma collection industry. These forward-looking statements also involve risks and uncertainties concerning the anticipated benefits and synergies of the recently completed acquisition transaction with Biotest, anticipated future combined businesses, operations, products and services, and liquidity, debt refinancing and/or repayment and capital return expectations, as well as ADMA’s ability to raise capital following closing of the Biotest transaction. Actual events or results may differ materially from those described in this document due to a number of important factors. These factors include, but are not limited to, the outcome of regulatory reviews with respect to the acquired BTBU assets, the ability of ADMA to successfully integrate the acquired therapy business, operations (including manufacturing and supply operations), sales and distribution channels, business and financial systems and infrastructures, research and development, technologies, products, services and employees; the ability of the parties to retain their customers and suppliers; the ability of the parties to minimize the diversion of their managements’ attention from ongoing business matters; ADMA’s ability to manage the increased scale, complexity and globalization of its business, operations and employee base post-closing, among others. Forward-looking statements are subject to many risks and uncertainties 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 those risks and uncertainties described in our filings with the U.S. Securities and Exchange Commission, including our most recent reports on Forms 10-K, 10-Q and 8-K, and any amendments thereto. Therefore, 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 inherent in the forward-looking statements included herein, the inclusion of such information should not be regarded as a representation or warranty by ADMA or any other person that the objectives and plans of ADMA will be achieved in any specified time frame, if at all. 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.
|ADMA BIOLOGICS, INC. AND SUBSIDIARIES|
|CONSOLIDATED STATEMENTS OF OPERATIONS|
|Three and Six Months Ended June 30, 2017 and 2016|
|Three Months Ended June 30,||Six Months Ended June 30,|
|License and other revenue||35,709||35,709||71,417||71,417|
|Cost of product revenue||4,334,019||1,344,241||5,950,306||2,610,662|
|Research and development||1,358,409||3,399,889||2,551,136||5,427,601|
|Amortization of intangibles||73,021||-||73,021||-|
|General and administrative||4,435,650||1,724,163||8,713,034||3,432,033|
|TOTAL OPERATING EXPENSES||11,801,269||7,762,594||20,367,143||14,045,016|
|LOSS FROM OPERATIONS||(8,401,868||)||(5,490,850||)||(14,338,871||)||(9,649,386||)|
|OTHER INCOME (EXPENSE):|
|OTHER EXPENSE, NET||(634,627||)||(521,485||)||(1,234,587||)||(975,418||)|
|BASIC AND DILUTED LOSS PER COMMON SHARE||$||(0.55||)||$||(0.50||)||$||(1.06||)||$||(0.93||)|
|WEIGHTED AVERAGE COMMON SHARES OUTSTANDING:|
|Basic and Diluted||16,427,054||12,121,500||14,666,677||11,407,918|
|ADMA BIOLOGICS, INC. AND SUBSIDIARIES|
|CONDENSED CONSOLIDATED Balance Sheets:|
|June 30,||December 31,|
|Cash, cash equivalents and short-term investments||$||25,574,009||$||15,305,051|
|Prepaid expenses and other current assets||2,408,459||313,914|
|Assets held for sale||845,389||-|
|Total current assets||44,270,864||21,657,138|
|Property and equipment, net||28,626,668||94,567|
|Intangible assets, net||6,011,003||-|
|Assets to be transferred under purchase agreement||1,698,755||1,906,217|
|LIABILITIES AND STOCKHOLDERS' EQUITY (DEFICIT)|
|Accounts payable and accrued expenses||$||8,816,128||$||4,950,037|
|Current portion of notes payable||6,666,667||6,111,111|
|Other current liabilities||162,216||161,713|
|Total current liabilities||15,645,011||11,222,861|
|Oxford notes payable, net of discount||11,150,708||14,111,640|
|Deferred revenue, net of current portion||2,618,616||2,690,033|
|Note payable - related party, net of discount||14,827,148||-|
|Purchase price payable||12,621,844||-|
|Other non-current liabilities||93,937||117,813|
|TOTAL STOCKHOLDERS' EQUITY (DEFICIT)||27,681,989||(4,457,262||)|
|TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY (DEFICIT)||$||84,639,253||$||23,685,085|
CONTACT: Brian Lenz Vice President and Chief Financial Officer | 201-478-5552 | www.admabiologics.com INVESTOR RELATIONS CONTACT: Matthew Duffy Managing Director, LifeSci Advisors, LLC | 212-915-0685 |
Released August 11, 2017