ArQule, Inc.  

(Public, NASDAQ:ARQL)   Watch this stock  
Find more results for ARQL
2.73
-0.02 (-0.73%)
May 24 - Close
NASDAQ real-time data - Disclaimer
Currency in USD
Range 2.70 - 2.77
52 week 1.98 - 6.98
Open 2.77
Vol / Avg. 129,797.00/268,325.00
Mkt cap 170.96M
P/E     -
Div/yield     -
EPS -0.20
Shares 62.62M
Beta 1.27
Inst. own 64%
Aug 1, 2013
Q2 2013 ArQule, Inc. Earnings Release Add to calendar
May 20, 2013
ArQule, Inc. Annual Shareholder Meeting
May 8, 2013
Q1 2013 ArQule, Inc. Earnings Conference Call
May 8, 2013
Q1 2013 ArQule, Inc. Earnings Release
Apr 30, 2013
ArQule, Inc. at Needham Healthcare Conference
Mar 14, 2013
Q4 2012 ArQule, Inc. Earnings Conference Call
Mar 14, 2013
Q4 2012 ArQule, Inc. Earnings Release
Mar 6, 2013
ArQule, Inc. at Cowen Health Care Conference
Feb 26, 2013
ArQule, Inc. at RBC Capital Markets' Healthcare Conference
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Key stats and ratios

Q1 (Mar '13) 2012
Net profit margin -102.01% -29.86%
Operating margin -104.58% -31.32%
EBITD margin - -28.40%
Return on average assets -17.98% -8.65%
Return on average equity -29.38% -19.63%
Employees 97 -
Carbon Disclosure Rating - -

Address

19 Presidential Way
WOBURN, MA 01801-5140
United States - Map
+1-781-9940300 (Phone)
+1-781-3766019 (Fax)

Website links

External links

Analyst Estimates - MarketWatch
SEC Filings - EDGAR Online
Major Holders - MSN Money
Discussion Group - Google Finance

Description

ArQule, Inc. is a clinical-stage biotechnology company engaged in the research and development of cancer therapeutics. It employs technologies, such as its ArQule Kinase Inhibitor Platform to design and develop drugs. Its product is ARQ 197, an orally administered inhibitor of the c-Met receptor tyrosine kinase (c-Met). C-Met is a target for cancer therapy, based on its multiple roles in cancerous cell proliferation, tumor spread, new blood vessel formation and resistance to certain drug therapies. It has licensed commercial rights to ARQ 197 for human cancer indications to Daiichi Sankyo in the United States, Europe, South America and the rest of the world, excluding Japan and other Asian countries, where it has licensed commercial rights to Kyowa Hakko Kirin. In August 2011, Kyowa Hakko Kirin announced the initiation of the Phase III ATTENTION (Asian Trial of Tivantinib plus Erlotinib vs. Erlotinib for NSCLC without EGFR Mutation) trial of tivantinib in combination with erlotinib.

Officers and directors

Patrick J. Zenner Independent Chairman of the Board
Age: 65
Bio & Compensation  - Reuters
Peter S. Lawrence President, Chief Operating Officer
Age: 49
Bio & Compensation  - Reuters
Paolo Pucci Chief Executive Officer, Director
Age: 52
Bio & Compensation  - Reuters
Brian Schwartz M.D. Chief Medical Officer
Age: 51
Bio & Compensation  - Reuters
Timothy C. Barabe Independent Director
Age: 59
Bio & Compensation  - Reuters
Susan L. Kelley M.D. Independent Director
Age: 58
Bio & Compensation  - Reuters
Ronald M. Lindsay Ph.D. Independent Director
Age: 65
Bio & Compensation  - Reuters
Michael D. Loberg Ph.D. Independent Director
Age: 64
Bio & Compensation  - Reuters
William G Messenger D. Min. Independent Director
Age: 51
Bio & Compensation  - Reuters