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Last $44.27 USD
Change Today +1.24 / 2.88%
Volume 664.3K
As of 7:40 PM 06/30/15 All times are local (Market data is delayed by at least 15 minutes).

newlink genetics corp (NLNK) Snapshot

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52 Week High
04/9/15 - $58.73
52 Week Low
10/13/14 - $17.32
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Average Volume 10 Days
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Dividend Yield
Current Stock Chart for NEWLINK GENETICS CORP (NLNK)

newlink genetics corp (NLNK) Details

NewLink Genetics Corporation, a biopharmaceutical company, focuses on discovering, developing, and commercializing immunotherapeutic products to enhance treatment options for patients with cancer. Its portfolio includes biologic product candidates based on its HyperAcute immunotherapy technology, which is designed to stimulate the human immune system; and small-molecule product candidates that are focused on breaking the immune system's tolerance to cancer by inhibiting the indoleamine-(2,3)-dioxygenase pathway and the tryptophan-(2.3)-dioxygenase pathway. The company’s lead product candidate, HyperAcute Pancreas immunotherapy, is being studied in Phase III clinical trials in surgically-resected pancreatic cancer patients, as well as in patients with advanced pancreatic cancer. It is also developing HyperAcute Lung immunotherapy for treating advanced non-small cell lung cancer; and HyperAcute Melanoma immunotherapy for treating advanced melanoma, as well as HyperAcute immunotherapies for renal, prostate, and breast cancers. In addition, the company is developing IDO pathway inhibitors comprising indoximod and NLG919 for metastatic breast cancer and metastatic prostate cancer; NLG2101 for patients with metastatic breast cancer; NLG2102 for treating refractory malignant brain tumors; NLG2103 for patients with advanced melanoma; and NLG2014 for patients with metastatic pancreatic cancer. NewLink Genetics Corporation was founded in 1999 and is headquartered in Ames, Iowa.

130 Employees
Last Reported Date: 03/16/15
Founded in 1999

newlink genetics corp (NLNK) Top Compensated Officers

Founder, Chairman, Chief Executive Officer an...
Total Annual Compensation: $573.2K
President, Chief Operations Officer and Chief...
Total Annual Compensation: $453.6K
Chief Financial Officer, Executive Vice Presi...
Total Annual Compensation: $90.0K
Vice President of Business Development
Total Annual Compensation: $262.5K
Compensation as of Fiscal Year 2014.

newlink genetics corp (NLNK) Key Developments

W. Jay Ramsey Retires as Quality Assurance Officer and as an Officer of Newlink Genetics Corporation

On May 22, 2015, W. Jay Ramsey, M.D., Ph.D. retired as Quality Assurance Officer and as an officer of NewLink Genetics Corporation. In connection with Dr. Ramsey's retirement, the company and Dr. Ramsey entered into a letter agreement, dated as of May 22, 2015.

NewLink Genetics Corporation Presents at Jefferies 2015 Global Healthcare Conference, Jun-03-2015 02:00 PM

NewLink Genetics Corporation Presents at Jefferies 2015 Global Healthcare Conference, Jun-03-2015 02:00 PM. Venue: The Grand Hyatt Hotel, New York, New York, United States.

NewLink Genetics Corporation Provides Update on Phase 3 Pancreatic Cancer Trial

NewLink Genetics Corporation announced the continuation without any modification or sample size adjustment for its pivotal, Phase 3 IMmunotherapy for Pancreatic RESectable cancer Study, called "IMPRESS," of algenpantucel-L for patients with surgically resected pancreatic cancer following the second planned interim data analysis. IMPRESS is a multi-center, open-label clinical trial assessing the safety and efficacy of algenpantucel-L, NewLink Genetics' HyperAcute® Pancreatic Cancer immunotherapy candidate, conducted in more than 70 leading cancer centers. With 722 patients enrolled, IMPRESS is the large trial to be completed in the United States for patients with resected pancreatic cancer. Algenpantucel-L has received fast-track status and orphan drug designation from the U.S. Food and Drug Administration (FDA). NewLink Genetics and the FDA reached agreement in January 2010 on a Special Protocol Assessment (SPA) on the trial design, clinical endpoints and statistical analyses plan for IMPRESS to be used in support of a Biologic License Application (BLA). After careful consideration, including a series of communications with the FDA regarding the statistical analysis plan, the Company decided to retain the benefit of the SPA and not to change the statistical analysis plan as defined in the original protocol. For the second interim analysis, the independent data safety monitoring committee (DSMC) reviewed available patient data with the originally planned log-rank analysis and sample size recalculation, in all respects consistent with the SPA. No other statistical methods were used. The DSMC recommended the study proceed without any modifications, including sample size adjustment, to final analysis. Therefore the Company believes the trial remains powered to determine efficacy upon the occurrence of 444 events.


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Price/Earnings 11.2x
Price/Sales 5.7x
Price/Book 5.3x
Price/Cash Flow 10.0x
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