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Liquidity and management's plans
6 Months Ended
Jun. 30, 2014
Accounting Policies [Abstract]  
Liquidity and management's plans

2. Liquidity and management’s plans:

Since inception, the Company has financed its operations principally from the sale of equity securities, proceeds from short-term borrowings or convertible notes, funded research arrangements and revenue generated as a result of its worldwide license and development agreement with Meda regarding ONSOLIS® and revenue generated as a result of its January 2012 agreement with Endo regarding its BEMA® Buprenorphine product candidate. The Company intends to finance its research and development, commercialization and working capital needs from existing cash, royalty revenue, new sources of debt and equity financing, existing and new licensing and commercial partnership agreements and, potentially, through the exercise of outstanding Common Stock options and warrants to purchase Common Stock.

Significant new financing and operating sources during the six months ended June 30, 2014 consisted of:

 

    approximately $58.2 million in net proceeds from certain institutional investors related to a definitive securities purchase agreement (see note 9);

 

    approximately $3.9 million in net proceeds via an “at-the-market” offering program utilizing the Company’s universal shelf registration (see note 9);

 

    approximately $21.9 million in contract revenue under the Endo agreement (see note 4);

 

    approximately $10.8 million in research and development reimbursements under the Endo agreement (see note 4);

 

    approximately $0.4 million in net royalties under the Meda agreements;

 

    approximately $2.8 million from the exercise of stock options; and

 

    approximately $4.0 million from the exercise of warrants.

Significant new financing and operating sources during the year ended December 31, 2013 consisted of:

 

    approximately $19.8 million in net proceeds from a secured loan facility from MidCap Financial SBIC, LP, as agent and lender (“MidCap”) (see note 7);

 

    approximately $2.8 million in research and development reimbursements under the Endo agreement;

 

    approximately $1.8 million in net royalties under the Meda agreements;

 

    approximately $0.3 million in contract revenue from licensing and supply agreement (see note 6); and

 

    approximately $0.4 million from the exercise of stock options and warrants.

At June 30, 2014, the Company had cash and cash equivalents of approximately $78.4 million. The Company used $8.7 million of cash from operations during the six months ended June 30, 2014. As of June 30, 2014, the Company had stockholders’ equity of $61.8 million, versus deficit of $(0.8) million at December 31, 2013. The Company believes that existing cash as of the date of this Quarterly Report, together with the June 6, 2014 approval and the upcoming commercialization of BUNAVAIL™ , and, the BEMA® Buprenorphine program’s expected regulatory milestones is sufficient to fully fund the Company’s planned level of operations through the end of 2015.

Additional capital may be required to support commercialization activities for BUNAVAIL™, including sales force sizing, the clinical development of Clonidine Topical Gel for painful diabetic neuropathy, the final regulatory activities prior to the relaunch of ONSOLIS®, for potential new product acquisitions or in-licenses, and for general working capital. Based on product development timelines and agreements with the Company’s development partners, the ability to scale up or reduce personnel and associated costs are factors considered throughout the product development life cycle. Also, available capital may be consumed more rapidly than currently anticipated, resulting in the need for additional funding. In addition, there can be no assurance that additional funding, when and if required, will be available at commercially available terms, if at all.