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NewLink Genetics Corporation Reports Second Quarter 2012 Financial Results

Recap of Data From Phase-2 HyperAcute® Pancreas (algenpantucel-L) Immunotherapy Trial:

Treated patients demonstrated statistically significant improvement in 12-month disease free survival and there was a strong suggestion of improvements in 12 month overall survival (OS) (observed 86% v. predicted 63% indicating a 37% improvement). Kaplan-Meier analysis suggests the improvement in OS increases over time with the 2-year and 3-year observed survival rates of 51% and 42% suggesting relative improvement of 59% and 121% in comparison to expected survival of 32% and 19% predicted by nomogram analysis.

Upcoming Activities

NewLink expects to present at the following investor conferences:
  • 2 nd Annual Canaccord Global Growth Conference, August 14-16, in Boston, MA.
  • Stifel Nicolaus Weisel Healthcare Conference 2012, September 4-7, in Boston, MA.
  • Robert W. Baird Health Care Conference, September 5-6, in New York City.
  • 9 th Annual Lazard Capital Markets Healthcare Conference, November 13-14, in New York City.

About NewLink Genetics Corporation

NewLink Genetics Corporation is a biopharmaceutical company focused on discovering, developing and commercializing novel immunotherapeutic products to improve cancer treatment options for patients and physicians. NewLink's portfolio includes biologic and small-molecule immunotherapy product candidates intended to treat a wide range of oncology indications. NewLink's product candidates are designed with an objective to harness multiple components of the innate immune system to combat cancer, either as a monotherapy or in combination with current treatment regimens, without incremental toxicity. NewLink's lead product candidate, HyperAcute® Pancreas cancer immunotherapy (algenpantucel-L) is being studied in a Phase 3 clinical trial in surgically-resected pancreatic cancer patients (patient information is available at ). This clinical trial is being performed under a Special Protocol Assessment with the U.S. Food and Drug Administration. NewLink and its collaborators have completed patient enrollment for a Phase 1/2 clinical trial evaluating its HyperAcute® Lung cancer immunotherapy (tergenpumatucel-L) product candidate for non-small cell lung cancer and a Phase 2 clinical trial for its HyperAcute® Melanoma cancer immunotherapy product candidate. NewLink also is developing indoximod (d-1-methyltryptophan, or D-1MT), a small-molecule, orally bioavailable product candidate from NewLink's proprietary indoleamine-(2, 3)-dioxygenase, or IDO, pathway inhibitor technology. Through NewLink's collaboration with the National Cancer Institute, NewLink is studying indoximod in various chemotherapy and immunotherapy combinations in two Phase 1B/2 safety and efficacy clinical trials. For more information please visit .

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements of NewLink that involve substantial risks and uncertainties. All statements, other than statements of historical facts, contained in this press release are forward-looking statements, within the meaning of The Private Securities Litigation Reform Act of 1995. The words "anticipate," "believe," "estimate," "expect," "intend," "may," "plan,""target," "potential," "will,""could," "should,""seek," or the negative of these terms or other similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. These forward-looking statements include, among others, statements about: NewLink's financial guidance for 2012; the timing for completion of enrollment of our Phase 3 clinical trial for our HyperAcute Pancreas cancer immunotherapy; the timing of release of clinical data from ongoing clinical studies; its plans related to moving additional indications into clinical development; NewLink's future financial performance, results of operations or sufficiency of capital resources to fund its operating requirements; and any other statements other than statements of historical fact. Actual results or events could differ materially from the plans, intentions and expectations disclosed in the forward-looking statements that NewLink makes due to a number of important factors, including those risks discussed in "Risk Factors" and elsewhere in NewLink's Annual Report on Form 10-K for the period ended December 31, 2011, in its Quarterly Report on Form 10-Q for the period ended June 30, 2012, and in its other filings with the Securities and Exchange Commission. The forward-looking statements in this press release represent NewLink's views as of the date of this press release. NewLink anticipates that subsequent events and developments will cause its views to change. However, while it may elect to update these forward-looking statements at some point in the future, it specifically disclaims any obligation to do so. You should, therefore, not rely on these forward-looking statements as representing NewLink's views as of any date subsequent to the date of this press release.
NewLink Genetics Corporation
Condensed Consolidated Statements of Operations
(In thousands, except share and per share amounts)
  Three Months Ended Six Months Ended
  June 30, June 30, June 30, June 30,
  2012 2011 2012 2011
Grant revenue $590 $537 $1,061 $1,141
Operating expenses:        
Research and development 4,740 3,795 8,570 6,975
General and administrative 2,151 1,136 3,609 2,452
Loss from operations (6,301) (4,394) (11,118) (8,286)
Other (expense) income, net (8) (33) (6)
Net loss $(6,309) $(4,394) $(11,151) $(8,292)
Net loss attributable to NewLink $(6,309) $(4,394) $(11,151) $(8,291)
Net loss per common share, basic and diluted $(0.31) $(1.20) $(0.54) $(2.28)
Weighted average number of common shares outstanding 20,684,944 3,646,973 20,649,045 3,641,539

NewLink Genetics Corporation
Condensed Consolidated Balance Sheets
(In thousands, except share and per share amounts)
  June 30, December 31,
  2012 2011
Current assets:    
Cash, cash equivalents and certificates of deposit $31,074 $41,980
Prepaid expenses and other current assets 1,797 808
Total current assets 32,871 42,788
Property and equipment, net 6,265 5,591
Total assets $39,136 $48,379
Liabilities and Equity    
Current liabilities:    
Accounts payable and accrued expenses $2,341 $3,537
Deferred rent 71 913
Other current liabilities 204 6,214
Total current liabilities 2,616 10,664
Long-term liabilities:    
Royalty obligation payable 6,000
Notes payable and obligations under capital leases, excluding current portion 854 942
Deferred rent, excluding current portion 1,434
Total long-term liabilities 8,288 942
Total liabilities 10,904 11,606
Stockholders' equity:    
Preferred Stock
Common stock 208 206
Additional paid-in capital 120,651 118,043
Deficit accumulated during the development stage (92,627) (81,476)
Total NewLink Genetics stockholders' equity 28,232 36,773
Total equity 28,232 36,773
Total liabilities and equity $39,136 $48,379
CONTACT: Gordon Link
         Chief Financial Officer

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