SRPT Share Price

Open 32.06 Change Price %
High 32.82 1 Day 0.69 2.15
Low 31.22 1 Week 4.03 14.05
Close 32.71 1 Month 1.88 6.10
Volume 2906453 1 Year 19.44 146.50
52 Week High 63.73
52 Week Low 8.00
SRPT Important Levels
Resistance 2 34.19
Resistance 1 33.58
Pivot 32.25
Support 1 31.84
Support 2 31.23
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Sarepta Therapeutics, Inc. (NASDAQ: SRPT)

SRPT Technical Analysis 3
As on 27th Feb 2017 SRPT Share Price closed @ 32.71 and we RECOMMEND Buy for LONG-TERM with Stoploss of 29.61 & Buy for SHORT-TERM with Stoploss of 30.73 we also expect STOCK to react on Following IMPORTANT LEVELS.
SRPT Target for February
1st Target up-side 37.69
2nd Target up-side 42.33
3rd Target up-side 46.98
1st Target down-side 24.43
2nd Target down-side 19.79
3rd Target down-side 15.14
SRPT Other Details
Segment EQ
Market Capital 539801792.00
Sector Healthcare
Industry Biotechnology
Offical website http://www.sareptatherapeutics.com
SRPT Address
SRPT
215 First Street
Suite 415
Cambridge, MA 02142
United States
Phone: 857-242-3700
Interactive Technical Analysis Chart Sarepta Therapeutics, Inc. ( SRPT NASDAQ USA )
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SRPT Business Profile
Sarepta Therapeutics Inc., formerly AVI BioPharma, Inc., biopharmaceutical company focused on the discovery and development of ribonucleic acid (RNA)-based therapeutics for the treatment of rare and infectious diseases. Its product candidates include Eteplirsen, AVI-6002, AVI-6003, and AVI-7100. As of December 31, 2011, the Company primarily focused on advancing the development of its Duchenne muscular dystrophy drug candidates, including its lead product candidate, eteplirsen, which is in a Phase IIb trial. It is also focused on developing therapeutics for the treatment of infectious diseases, including its lead infectious disease programs aimed at the development of drug candidates for the Ebola and Marburg hemorrhagic fever viruses. program focuses on the development of disease-modifying therapeutic candidates for Duchenne muscular dystrophy (DMD). It initiated a Phase IIb trial for eteplirsen in August 2011 with an objective of initiating a pivotal trial subsequent to 2011.