Trubion Pharmaceuticals Inc. Reports First Quarter 2008 Results

SEATTLE, May 8 /PRNewswire-FirstCall/ -- Trubion Pharmaceuticals Inc. today announced financial results for its first quarter ended March 31, 2008.

First Quarter 2008 Financial Results

Revenue for the first quarter ended March 31, 2008, was $4.0 million, compared with $4.8 million in 2007. The decrease was primarily due to an extension of the recognition of the up-front fee and a slight decrease in reimbursement revenue from the Wyeth collaboration related to the Phase 2b clinical trial for our lead product candidate, TRU-015 for rheumatoid arthritis (RA).

Revenue in the three months ended March 31, 2008 and 2007, included $1.5 million and $2 million, respectively, for amortization of the $40 million up-front fee from the Wyeth collaboration. This up-front fee is being deferred and recognized on a straight-line basis over the estimated term of the research and development service period of six years and three months.

Total operating expenses for the first quarter ended March 31, 2008, were $10.5 million, compared with $10.9 million in 2007. The decrease was primarily due to lower outside manufacturing costs for TRU-016. The decrease was partially offset by increased personnel-related expenses.

Net loss for the first quarter ended March 31, 2008, was $6.0 million, or $0.33 per diluted common share, compared with a net loss of $5.0 million, or $0.29 per diluted common share, in 2007.

Trubion had $72.1 million in cash, cash equivalents and investments as of March 31, 2008, compared with $78.5 million as of December 31, 2007.

“We have already achieved several important milestones in 2008 in advancing the clinical development of our alliance-based and proprietary therapeutic compounds for autoimmune and inflammatory diseases and cancer,” said Peter Thompson, M.D., FACP, Trubion’s president, chief executive officer and chairman. “We look forward to continued advancement of both our clinical and preclinical programs throughout the rest of the year.”

2008 Financial Guidance

Trubion anticipates 2008 revenues to be in the range of $15 million to $20 million earned through the company’s Wyeth collaboration. Total operating expenses are expected to be approximately $53 million to $58 million for 2008. The planned increase in 2008 operating expenses is primarily attributable to clinical trial expenses associated with the retreatment study being completed by Trubion for its lead product candidate, TRU-015, manufacturing and clinical costs associated with its TRU-016 product candidate, and increased personnel-related expense. Operating cash requirements in 2008 are expected to be approximately $35 million to $40 million.

Conference Call Details

Trubion will host a conference call and webcast to discuss its first quarter 2008 financial results. The call will be held today at 2 p.m. Pacific time (5 p.m. Eastern time). The live event will be available from Trubion’s Web site at http://investors.trubion.com/events.cfm, or by calling (877) 545-1488 or (719) 325-4899. Beginning later today, a replay of the discussion will be available from Trubion’s Web site or by calling (888) 203-1112 or (719) 457-0820 and entering 7602146. Replay will be available at 8 p.m. EDT until midnight, Monday, May 12. The webcast replay will be available in the events section of Trubion’s Web site.

About Trubion

Trubion is a biopharmaceutical company that is creating a pipeline of novel protein therapeutic product candidates to treat autoimmune and inflammatory diseases and cancer. The company’s mission is to develop a variety of first-in-class and best-in-class product candidates, customized for optimal safety, efficacy, and convenience that it believes may offer improved patient experiences. Trubion’s current product candidates are novel single-chain protein, or SMIP(TM), therapeutics, and are designed using its custom drug assembly technology. Trubion’s product pipeline includes CD20-directed candidates such as TRU-015 and SBI-087 for autoimmune and inflammatory diseases, developed under the company’s Wyeth collaboration. Trubion’s product pipeline also includes Trubion’s proprietary product candidate, TRU-016, a novel CD37-targeted therapy for the treatment of B-cell malignancies that is currently in Phase 1/2 clinical evaluation. In addition to Trubion’s current product candidates, the company is also developing additional alliance and proprietary product candidates that build on its product development experience. More information is available in the investors section of Trubion’s website: investors.trubion.com.

Forward-Looking Statements

Certain statements in this release may constitute “forward-looking statements” within the meaning of Section 21E of the Securities Exchange Act of 1934 and Section 27A of the Securities Act of 1933. These statements include, but are not limited to, those related to the company’s future clinical development programs and the timing thereof, the company’s future regulatory filings and the timing and outcome thereof and the company’s expected financial and operating results. These statements are based on current expectations and assumptions regarding future events and business performance and involve certain risks and uncertainties that could cause actual results to differ materially. These risks include, but are not limited to, risks associated with the company’s Wyeth collaboration, including Wyeth’s control over development timelines, the risks that the Company is unable to advance its clinical development programs and regulatory applications and action at the rate it expects, the risk that the Company does not achieve the financial and operating results it expects, and such other risks as identified in the company’s quarterly report on Form 10-Q for the period ended March 31, 2008, and from time to time in other reports filed by Trubion with the U.S. Securities and Exchange Commission. These reports are available on the Investors page of the company’s corporate Web site at http://www.trubion.com. Trubion undertakes no duty to update any forward-looking statement to conform the statement to actual results or changes in the company’s expectations.

CONTACT: Jim DeNike, Senior Director, Corporate Communications of Trubion
Pharmaceuticals Inc., +1-206-838-0500, jdenike@trubion.com; or Amy Petty,
Senior Account Executive of Waggener Edstrom Healthcare, +1-617-576-5788,
amyp@waggeneredstrom.com, for Trubion Pharmaceuticals Inc.

Web site: http://www.trubion.com/
http://investors.trubion.com/events.cfm//

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