ARIA Share Price

Open 13.25 Change Price %
High 13.25 1 Day -0.93 -6.79
Low 12.32 1 Week -0.31 -2.37
Close 12.76 1 Month 3.49 37.65
Volume 9331212 1 Year 6.54 105.14
52 Week High 14.42
52 Week Low 0.00
ARIA Important Levels
Resistance 2 13.62
Resistance 1 13.27
Pivot 12.78
Support 1 12.25
Support 2 11.90
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ARIAD Pharmaceuticals, Inc. (NASDAQ: ARIA)

ARIA Technical Analysis 4
As on 7th Dec 2016 ARIA Share Price closed @ 12.76 and we RECOMMEND Strong Buy for LONG-TERM with Stoploss of 8.60 & Buy for SHORT-TERM with Stoploss of 12.19 we also expect STOCK to react on Following IMPORTANT LEVELS.
ARIA Target for December
1st Target up-side 16.64
2nd Target up-side 18.85
3rd Target up-side 21.06
1st Target down-side 10.32
2nd Target down-side 8.11
3rd Target down-side 5.9
ARIA Other Details
Segment EQ
Market Capital 3671460096.00
Sector Healthcare
Industry Biotechnology
Offical website http://www.ariad.com
ARIA Address
ARIA
26 Landsdowne Street
Cambridge, MA 02139
United States
Phone: 617-494-0400
Fax: 617-494-8144
Interactive Technical Analysis Chart ARIAD Pharmaceuticals, Inc. ( ARIA NASDAQ USA )
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ARIA Business Profile
ARIAD Pharmaceuticals, Inc. (ARIAD), incorporated on on April 12, 1991, is a global oncology company focused on the discovery, development and commercialization of medicines for the cancer patients. ARIAD’s first medicine, Iclusig, is approved in the United States for the treatment of adult patients with chronic, accelerated or blast phase chronic myeloid leukemia that is resistant or intolerant to prior tyrosine kinase inhibitor (TKI) therapy or Philadelphia chromosome-positive acute lymphoblastic leukemia that is resistant or intolerant to prior TKI therapy. As of January 11, 2013, additional clinical trials of Iclusig in other cancers were ongoing. As of January 11, 2013, ARIAD also studied AP26113, another molecularly targeted medicine, in certain forms of lung cancer. As of January 11, 2013, the Company’s pipeline contained four compounds: ponatinib, AP26113, ridaforolimus and AP1903. AP26113 is a potent dual inhibitor of anaplastic lymphoma kinase (ALK) and epidermal growth factor receptor (EGFR). AP1903 is a dimerizer drug licensed to Bellicum Pharmaceuticals, Inc. In December 2012, the Company was granted accelerated approval of Iclusig ponatinib for the treatment of adult patients with chronic, accelerated or blast phase chronic myeloid leukemia (CML) that is resistant or intolerant to prior tyrosine kinase inhibitor (TKI) therapy or Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ ALL) that is resistant or intolerant to prior TKI therapy. Ponatinib is a BCR-ABL inhibitor that also selectively inhibits certain other tyrosine kinases in preclinical studies, including FLT3, RET, KIT, and the members of the FGFR, PDGFR and VEGFR families of kinases. The EPIC (Evaluation of Ponatinib versus Imatinib inChronic Myeloid Leukemia) trial is designed to provide definitive clinical data to support regulatory approval of ponatinib in treatment-nave CML patients. The PACE (Ponatinib Ph+ ALL and CML Evaluation) trial is a pivotal Phase 2 clinical trial of the Company’s investigational pan-BCR-ABL inhibitor, ponatinib (formerly AP24534).