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PALATINE, Ill., Sept. 16, 2019 (GLOBE NEWSWIRE) -- Acura Pharmaceuticals, Inc., a specialty pharmaceutical company engaged in the research, development and commercialization of technologies and product candidates intended to mitigate the risk of outcomes associated with product misuse announced today financial results for the three and twelve months ended December 31, 2018.
The Company reported a net loss of $3.8 million or ($0.18) per diluted share for 2018 compared to a net loss of $5.7 million or ($0.36) per diluted share for 2017. For the fourth quarter 2018 the Company reported net income of $8 thousand or $0.00 per diluted share, compared to a net loss of $1.7 million or (0.08) per diluted share for the same period in 2017.
The Company recorded royalty revenue of $0.4 million and $0.3 million for the twelve month periods ended December 31, 2018 and 2017, respectively, and $0.1 million and $0.1 million in royalty revenue for the three months ended December 31, 2018 and 2017, respectively.
Research and development costs and expenses from our development facility and product candidates were $1.8 million for the twelve month period ended December 31, 2018, compared to $3.7 million for the same period in 2017. These expenses were $0.1 million for the fourth quarter 2018, compared to $0.9 million for the same period in 2017.
General and administrative expenses were $2.6 million for the twelve month period ended December 31, 2018, versus $4.3 million in the same period last year which includes selling and marketing expenses we incurred with respect to the Nexafed product line during the first half of 2017. We out-licensed this product line in March of 2017 and discontinued selling efforts at that time. General and administrative expenses were $0.2 million for the fourth quarter 2018, compared to $0.9 million for the same period in 2017.
The Company delayed filing the Form 10-K for 2018 pending the completion of the License, Development and Commercialization Agreement (the “Agreement”) with Abuse Deterrent Pharmaceuticals, LLC (”AD Pharma”) for our lead product candidate, LTX-03 (hydrocodone bitartrate with acetaminophen immediate-release tablets utilizing Acura’s patented LIMITx™ technology). We entered into the Agreement at June 28, 2019. The Agreement is described in our press release dated July 2, 2019 and our Form 8-K filed July 5, 2019. This Agreement provided the capital necessary to fund ongoing operations, including the expense associated with our annual audit and quarterly SEC filings. The Company plans to file the first and second quarter 2019 Form 10-Qs as quickly as possible and then return to timely submission of our required SEC filings.
As of September 12, 2019, the Company had cash of $0.75 million. Additionally, the Agreement provides that AD Pharma will pay the Company monthly license payments of $350,000 from July 2019 through November 2020, subject to AD Pharma’s right to terminate such payments, and pay all outside development costs for LTX-03. We expect these amounts will fund operations through 2020.
About Acura Pharmaceuticals
Acura Pharmaceuticals is a specialty pharmaceutical company engaged in the research, development and commercialization of technologies and product candidates intended to mitigate the risk of outcomes associated with product misuse. The Company has three proprietary technologies: LIMITx™ Technology, AVERSION® Technology and IMPEDE® Technology.
LIMITx™ Technology utilizes acid neutralizing ingredients to precisely control gastric acidity, which limits the release of drug from tablets and its subsequent systemic absorption when multiple tablets are ingested. LIMITx™ Technology is useful with products whose side effect risks can be mitigated by limiting exposure to a drug in overdose situations.
AVERSION® Technology, used in the FDA approved drug OXAYDO® (oxycodone HCl) marketed by Zyla Life Sciences, utilizes polymers designed to limit the abuse of the product by nasal snorting and injection. AVERSION® Technology is also licensed to KemPharm for use in certain of their products.
IMPEDE® Technology, used in NEXAFED® (pseudoephedrine HCl) and NEXAFED® Sinus (pseudoephedrine HCl/acetaminophen) marketed by MainPointe Pharmaceuticals, utilizes polymers and other ingredients to disrupt the extraction and processing of pseudoephedrine from the tablets into methamphetamine.
Certain statements in this press release constitute “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Such forward-looking statements involve known and unknown risks, uncertainties and other factors which may cause our actual results, performance or achievements to be materially different from any future results, performance, or achievements expressed or implied by such forward-looking statements. Forward-looking statements may include, but are not limited to:
In some cases, you can identify forward-looking statements by terms such as "may," “will”, "should," "could," "would," "expects," "plans," "anticipates," "believes," "estimates," “indicates”, "projects," “predicts," "potential" and similar expressions intended to identify forward-looking statements. These statements reflect our current views with respect to future events and are based on assumptions and subject to risks and uncertainties. Given these uncertainties, you should not place undue reliance on these forward-looking statements. We discuss many of these risks in greater detail in our filings with the Securities and Exchange Commission.
ACURA PHARMACEUTICALS, INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
|December 31,||December 31,|
|Assets - current||$||461||$||2,566|
|Property, plant and equipment, net||606||679|
|Liabilities - current||$||1,435||$||1,237|
|Accrued interest - current portion||-||700|
|Debt – current, net||-||2,694|
|Accrued interest to related party, non-current portion||110||-|
|Debt to related party - non-current portion, net||4,224||-|
|Total liabilities and stockholders' deficit||$||2,152||$||4,604|
ACURA PHARMACEUTICALS, INC.
CONSOLIDATED STATEMENTS OF LOSS (INCOME)
(in thousands, except per share amounts)
Twelve Months Ended
Three Months Ended
|License fee revenue||$||-||$||2,500||$||-||$||-|
|Total revenues, net||410||2,966||63||74|
|Cost and expenses:|
|Cost of sales (excluding inventory provisions)||-||128||-||-|
|Research and development||1,759||3,721||83||913|
|Selling, marketing, general and administrative||2,566||4,342||234||915|
|Total cost and expenses||4,325||8,191||317||1,828|
|Operating (loss) income||(3,915||)||(5,225||)||(254||)||(1,754||)|
|Non-operating income (expense):|
|Interest expense, net||(223||)||(592||)||(34||)||(119||)|
|Total other income (expense), net||73||(592||)||262||(119||)|
|(Loss) income before income taxes||(3,842||)||(5,817||)||8||(1,873||)|
|Provision for income taxes||-||(135||)||-||(135||)|
|Net (loss) income||$||(3,842||)||$||(5,682||)||8||$||(1,738||)|
|Loss per share:|
|Weighted average number of shares outstanding:|