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Synergy Pharmaceuticals Reports 2012 Fourth Quarter And Full-Year Financial Results

Synergy had approximately 67 million common shares outstanding at December 31, 2012.

About Synergy Pharmaceuticals Inc.

Synergy is a biopharmaceutical company focused on the development of new drugs to treat gastrointestinal disorders and diseases. Synergy's lead proprietary drug candidate plecanatide is a synthetic analog of the human gastrointestinal (GI) hormone uroguanylin, and functions by activating the guanylate cyclase C receptor on epithelial cells of the GI tract. Synergy previously completed a Phase I study of plecanatide in healthy volunteers, a Phase IIa clinical trial in CIC patients. On January 2, 2013, Synergy announced positive results in a large multicenter clinical trial of plecanatide to treat CIC. Plecanatide is also being developed to treat patients with IBS-C. Synergy's second GC-C agonist SP-333 is in clinical development to treat inflammatory bowel diseases, and is presently in a Phase I trial in healthy volunteers. More information is available at .

Forward-Looking Statements

Certain statements in this press release are forward-looking within the meaning of the Private Securities Litigation Reform Act of 1995. These statements may be identified by the use of forward-looking words such as "anticipate," "planned," "believe," "forecast," "estimated," "expected," and "intend," among others. These forward-looking statements are based on Synergy's current expectations and actual results could differ materially. There are a number of factors that could cause actual events to differ materially from those indicated by such forward-looking statements. These factors include, but are not limited to, substantial competition; our ability to continue as a going concern; our need for additional financing; uncertainties of patent protection and litigation; uncertainties of government or third party payer reimbursement; limited sales and marketing efforts and dependence upon third parties; and risks related to failure to obtain FDA clearances or approvals and noncompliance with FDA regulations. As with any pharmaceutical under development, there are significant risks in the development, regulatory approval and commercialization of new products. There are no guarantees that future clinical trials discussed in this press release will be completed or successful or that any product will receive regulatory approval for any indication or prove to be commercially successful. Investors should read the risk factors set forth in Synergy's Form 10-K for the year ended December 31, 2012 and other periodic reports filed with the Securities and Exchange Commission. While the list of factors presented here is considered representative, no such list should be considered to be a complete statement of all potential risks and uncertainties. Unlisted factors may present significant additional obstacles to the realization of forward-looking statements. Forward-looking statements included herein are made as of the date hereof, and Synergy does not undertake any obligation to update publicly such statements to reflect subsequent events or circumstances.
Condensed Consolidated Balance Sheets ($ in thousands)
(unaudited) December 31, 2012 December 31, 2011
Cash, cash equivalents and short term available for sale securities $32,502 $13,245
Prepaid expenses and other current assets 1,547 1,063
Total current assets 34,049 14,308
Other assets 3,356 1,562
Total assets $37,405 $15,870
Liabilities and Stockholders' Equity    
Accounts payable 5,255 $1,416
Accrued expenses 2,060 1,331
Total current liabilities 7,315 2,747
Derivative financial instruments -warrants 5,258 3,325
Total Liabilities 12,573 6,072
Total stockholders' equity 24,832 9,798
Total liabilities and stockholders' equity $37,405 $15,870
Condensed Consolidated Statement of Operations        
($ in thousands except shares, and per share data) Three Months ended December 31, 2012 Three Months ended December 31, 2011 Year ended December 31, 2012 Year Ended December 31, 2011
Revenues $  -- $  -- $  -- $  --
Costs and Expenses:        
Research and development 9,085 5,703 29,294 13,419
Purchased in-process research and development -- -- 1,000 --
General and administrative 2,447 2,222 7,941 6,745
Loss from Operations (11,532) (7,925) (38,235) (20,164)
Other income 250 362 506  362
Interest and investment income 68 26 218 90
Interest expense -- -- -- (12)
Change in Fair Value of Financial Instruments (764) 1,911 (1,933) 5,257
Net Loss $(11,978) $(5,626) $(39,444) $(14,467)
Net Loss per common share, basic and diluted $ (0.18) $ (0.12) $ (0.64) $ (0.30)
Weighted Average Common Shares Outstanding (a) 66,194,306 48,657,013 61,702,277 47,598,240
CONTACT: Investor Contact Information:
         Danielle Spangler
         The Trout Group
         (646) 378-2924

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