SAN DIEGO, Feb. 20 /PRNewswire-FirstCall/ -- Anadys Pharmaceuticals, Inc. , a biopharmaceutical company dedicated to improving patient care by developing novel medicines in the areas of hepatitis C and oncology, today reported its financial results and highlights for the fourth quarter and year ended December 31, 2007.
"In the fourth quarter we continued to advance our two development programs," said Steve Worland, Ph.D., President and Chief Executive Officer of Anadys. "Our IND for ANA773, an oral toll-like receptor 7 (TLR7) agonist prodrug for the treatment of cancer, was accepted by the FDA and we initiated a Phase I clinical trial to be conducted in patients with advanced solid tumors. We continued preclinical studies for ANA598, our non-nucleoside polymerase inhibitor for the treatment of hepatitis C, and remain on track to file the IND for this compound in the second quarter of 2008." Commenting on the outlook for 2008 and the impact of the Company's strategic restructuring undertaken in mid-2007, Dr. Worland added, "In the coming year we expect the cost savings from our restructuring will largely offset the increased development expenses for ANA598 and ANA773, resulting in planned cash utilization in 2008 approximately the same as in 2007."
Financial Results
The Company had revenues of $0.2 million for the fourth quarter of 2007, compared to $1.2 million for the fourth quarter of 2006. Revenues for the quarter ended December 31, 2007 were derived from the successful completion of our screening collaboration with Aphoenix, Inc. Revenues for the quarter ended December 31, 2006, were primarily derived from the amortization of an upfront payment and milestone payment previously received under our former collaboration with Novartis for the development of ANA975, which was discontinued in 2007.
Research and development expenses were $6.9 million for the fourth quarter of 2007 compared to $6.4 million for the fourth quarter of 2006. The $0.5 million increase was primarily due to an increase in external preclinical development costs for ANA598 and ANA773. The increase was partially offset by a decrease in development costs associated with ANA975 and cost savings associated with our restructuring.
General and administrative expenses were $1.8 million for the fourth quarter of 2007 compared to $3.5 million for the fourth quarter of 2006. The $1.7 million decrease is primarily due to a decrease in share-based compensation expense and, to a lesser extent, a decrease in personnel expenses.
Operating expenses were $8.8 million for the fourth quarter of 2007, compared to $9.9 million for the fourth quarter of 2006. Included as a component of Anadys' operating expenses was non-cash share-based expense of $0.6 million and $2.2 million for the three months ended December 31, 2007 and 2006, respectively.
Net loss was $7.8 million for the fourth quarter of 2007, compared to a net loss of $7.6 million for the fourth quarter of 2006. Basic and diluted net loss per common share was $0.27 in the fourth quarter of 2007 and 2006. Non-cash share-based expense resulted in a $0.02 and $0.08 decrease in basic and diluted net loss per share for the three months ended December 31, 2007 and 2006, respectively.
Revenues for the twelve months ended December 31, 2007 were $24.1 million compared to $5.4 million in 2006. Revenues for the twelve months ended December 31, 2007 were primarily attributable to the recognition of the remainder of the $20 million up-front payment and the $10 million IND milestone payment, each of which were received from Novartis in 2005. For the twelve months ended December 31, 2007, Anadys reported a net loss of $9.2 million compared to a net loss of $26.8 million for the prior year. The reduction in Anadys' cumulative operating losses for the twelve months ended December 31, 2007 compared to the same period in 2006 was almost entirely attributable to the termination of the ANA975 development program and the resulting recognition of deferred revenue from payments previously received from Novartis. Included as a component of net loss for the fourth quarter of 2007 were severance related costs of $0.9 million associated with our restructuring. Basic and diluted net loss per common share was $0.32 for the twelve months ended December 31, 2007, compared to $0.94 for the same period in 2006.
As of December 31, 2007, the Company's cash, cash equivalents and securities available-for-sale totaled $56.5 million.
Webcast of Conference Call
Anadys will host a conference call at 5:00 p.m. EST today to discuss its fourth quarter and year-end financial results and the status of its development programs. A live webcast of the call will be available online at http://www.anadyspharma.com. A telephone replay will also be available approximately one hour after completion of the call. To access the telephone replay, dial 888-286-8010 (domestic) or 617-801-6888 (international), passcode 63692537. The webcast and telephone replay will be available through March 5, 2008.
About Anadys
Anadys Pharmaceuticals, Inc. is a biopharmaceutical company dedicated to improving patient care by developing novel medicines in the areas of hepatitis C and oncology. The Company is developing ANA598, a small-molecule, non-nucleoside inhibitor of the NS5B polymerase for the treatment of chronic hepatitis C and ANA773, an oral TLR7 agonist prodrug for cancer.
Safe Harbor Statement
Statements in this press release that are not strictly historical in nature constitute "forward-looking statements." Such statements include, but are not limited to, references to the expected timing and planned development activities for ANA598 and ANA773, Anadys' expected cash utilization during 2008, the anticipated future clinical benefits of ANA598 and ANA773, and the ability to modulate immunostimulatory responses to ANA773 by schedule of administration and develop ANA773 as an anti-cancer agent. Such forward-looking statements involve known and unknown risks, uncertainties and other factors, which may cause Anadys' actual results to be materially different from historical results or from any results expressed or implied by such forward-looking statements. For example, the results of preclinical studies may not be predictive of future results, and Anadys cannot provide any assurances that ANA598 or ANA773 will not have unforeseen safety issues, will have favorable results in future clinical trials or will receive regulatory approval. In addition, Anadys' results may be affected by competition from other biotechnology and pharmaceutical companies, its effectiveness at managing its financial resources, its ability to successfully develop and market products, difficulties or delays in its preclinical studies or clinical trials, difficulties or delays in manufacturing its clinical trials materials, the scope and validity of patent protection for its products, regulatory developments involving future products and its ability to obtain additional funding to support its operations. Risk factors that may cause actual results to differ are more fully discussed in Anadys' SEC filings, including Anadys' Form 10-K for the year ended December 31, 2006 and Anadys' Form 10-Q for the quarter ended September 30, 2007. All forward-looking statements are qualified in their entirety by this cautionary statement. Anadys is providing this information as of this date and does not undertake any obligation to update any forward-looking statements contained in this document as a result of new information, future events or otherwise.
(1) Includes $36 and ($254) as additional (reduction in) research and development expense, which represents an estimate of the net payable due to (reimbursement by) Novartis of ANA975 research and development costs for the three months ended December 31, 2007 and 2006, respectively. Includes ($478) and ($3,677) as an offset in research and development expense, which represents an estimate of the net reimbursement by Novartis of ANA975 research and development costs for the twelve months ended December 31, 2007 and 2006, respectively.
(2) Includes non-cash operating expenses of $615 and $2,182 determined in accordance with Statement of Financial Accounts Standards No. 123(R), "Share-Based Payment" (SFAS No. 123(R)) or approximately $0.02 and $0.08 effect on basic and diluted net income (loss) per common share for the three months ended December 31, 2007 and 2006, respectively. Research and development expense and general and administrative expense includes $275 and $340 of non-cash operating expenses determined in accordance with SFAS No. 123(R) for the three months ended December 31, 2007. Includes non-cash operating expenses of $4,113 and $7,130 determined in accordance with Financial Accounts Standards Board Statement 123(R), "Share-Based Payment" or approximately $0.14 and $0.25 effect on basic and diluted net loss per common share for the twelve months ended December 31, 2007 and 2006, respectively. Research and development expense and general and administrative expense includes $2,463 and $1,650 of non-cash operating expenses determined in accordance with SFAS No. 123(R) for the twelve months ended December 31, 2007.
CONTACT: Investors, James T. Glover, SVP, Operations & CFO of Anadys
Pharmaceuticals, Inc., +1-858-530-3763, jglover@anadyspharma.com; or Media,
Ian Stone, ian.stone@russopartnersllc.com, or David Schull,
david.schull@russopartnersllc.com, +1-619-814-3510, both of Russo Partners,
LLC, for Anadys Pharmaceuticals, Inc.
Web site: http://www.anadyspharma.com/
