ALXA Share Price

Open 0.00 Change Price %
High 0.00 1 Day 0.00 0.00
Low 0.00 1 Week 0.00 0.00
Close 0.94 1 Month 0.00 0.00
Volume 100 1 Year -0.19 -16.81
52 Week High 1.23
52 Week Low 0.00
ALXA Important Levels
Resistance 2 0.94
Resistance 1 0.94
Pivot 0.31
Support 1 0.94
Support 2 0.94
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Alexza Pharmaceuticals, Inc. (NASDAQ: ALXA)

ALXA Technical Analysis 4
As on 20th Jun 2016 ALXA Share Price closed @ 0.94 and we RECOMMEND Buy for LONG-TERM with Stoploss of 0.85 & Strong Buy for SHORT-TERM with Stoploss of 0.75 we also expect STOCK to react on Following IMPORTANT LEVELS.
ALXA Target for October
1st Target up-side N/A
2nd Target up-side N/A
3rd Target up-side N/A
1st Target down-side N/A
2nd Target down-side N/A
3rd Target down-side N/A
ALXA Other Details
Segment EQ
Market Capital 64712160.00
Sector Healthcare
Industry Drug Manufacturers - Other
Offical website
ALXA Address
2091 Stierlin Court
Mountain View, CA 94043
United States
Phone: 650-944-7000
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ALXA Business Profile
Alexza Pharmaceuticals, Inc. (Alexza), incorporated on December 19, 2000, is a pharmaceutical company focused on the research, development and commercialization of products for the acute treatment of central nervous system (CNS) conditions. Alexza’s product candidates are based on its technology, the Staccato system. The Staccato system vaporizes an excipient-free drug to form a condensation aerosol that, when inhaled, allows for systemic drug delivery. As of December 31, 2011, the Company had screened more than 400 drug compounds, identifying approximately 200 drug compounds that demonstrate initial vaporization. The Company's product candidate is ADASUVE (Staccato loxapine). Its other product candidates in active development are AZ-007 (Staccato zaleplon) and Staccato nicotine. Its product candidates not in active development are AZ-104 (Staccato loxapine, low-dose), AZ-002 (Staccato alprazolam) and AZ-003 (Staccato fentanyl). In January 2011, Cypress was acquired by Royalty Pharma. Alexza is developing ADASUVE for the acute treatment of agitation in adults with schizophrenia or bipolar disorder. In August 2011, the Company resubmitted the ADASUVE NDA, which was accepted for filing by the Food and Drug Administration (FDA) as a complete, class 2 response to the FDA's CRL. The FDA indicated a Prescription Drug User Fee Act (PDUFA), goal date for the ADASUVE NDA of February 4, 2012. The Company has completed Phase I testing for AZ-007. This product candidate is being developed for the treatment of insomnia in patients who have difficulty falling asleep, including patients who awake in the middle of the night and have difficulty falling back asleep. In the Phase I study, AZ-007 delivered an IV-like pharmacokinetic profile with a median time to peak drug concentration of 1.6 minutes. During the year ended December 31, 2011, it completed the process development work to transfer AZ-007 from its original single-dose clinical product device to the current single-dose commercial product device.