MOUNTAIN VIEW, Calif.
Aug. 21, 2012
/PRNewswire/ -- Alexza Pharmaceuticals, Inc. (Nasdaq: ALXA) announced today that the company has received its EU Certificate of GMP Compliance of a Manufacturer. In
, Alexza hosted an EU GMP inspection, which was conducted by the Agencia Espanola de Medicamentos y Productos Sanitarios. Based upon the outcome from this inspection of the company's
Mountain View, CA
facility and additional Company responses, the Spanish authorities, on behalf of the EU, considered that the Alexza facility complies with the principles and guidelines of Good Manufacturing Practice set forth in Directive 2003/94/EC. The initial certificate is valid through
May 15, 2015
About Alexza Pharmaceuticals, Inc.
Alexza is a pharmaceutical company focused on the research, development and commercialization of novel, proprietary products for the acute treatment of central nervous system conditions. Alexza's technology, the Staccato
system, vaporizes unformulated drug to form a condensation aerosol that, when inhaled, allows for rapid systemic drug delivery through deep lung inhalation. With the
system, a drug is quickly absorbed through the lungs into the bloodstream, providing speed of therapeutic onset that is comparable to intravenous administration, but with greater ease, patient comfort and convenience. (Click
to see an animation of how the
loxapine) is Alexza's lead program, which is being developed for the acute treatment of agitation associated with schizophrenia or bipolar I disorder in adults. Alexza completed and announced positive results from both of its Phase 3 clinical trials and initially submitted the ADASUVE New Drug Application (NDA) in December 2009. In
, the Company received a complete response letter (CRL) from the U.S. Food and Drug Administration (FDA) regarding the application. The Company completed an end-of-review meeting with the FDA in
, a REMS guidance meeting with the FDA in
, and the ADASUVE NDA was resubmitted in August 2011. In
, the ADASUVE NDA was the subject of an advisory committee meeting. In
, Alexza received notice of a 90-day extension of the PDUFA goal date, from
February 4, 2012
, 2012. In
, Alexza received a second CRL from the FDA regarding the ADASUVE NDA and on
June 22, 2012
, the Company resubmitted the ADASUVE NDA. The resubmitted ADASUVE NDA has a PDUFA goal date of
December 21, 2012
, the Company established a commercial partnership for ADASUVE with
Grupo Ferrer Internacional
is a leading pharmaceutical company in
with extensive operations in the Americas, and is Alexza's partner in the commercialization of ADASUVE in
and the Commonwealth of Independent States countries. Alexza filed its ADASUVE Marketing Authorization Application (MAA) with the European Medicines Agency (EMA) in October 2011. In
, Alexza submitted its responses to the Committee for Medicinal Products for Human Use (CHMP) Consolidated List of Questions (Day 120 List of Questions). According to the published EMA timetables, Alexza expects to receive the Day 180 List of Outstanding Issues for the ADASUVE MAA in late
and Alexza currently projects that it will receive the Day 210 CHMP Opinion for the ADASVUE MAA in
For more information about Alexza, the
system technology or the Company's development programs, please visit
. ADASUVE™ is a registered trademark of Alexza Pharmaceuticals, Inc.
Safe Harbor Statement
This news release contains
forward-looking statements that involve significant risks and uncertainties. Any statement describing the Company's expectations or beliefs is a forward-looking statement, as defined in the Private Securities Litigation Reform Act of 1995, and should be considered an at-risk statement. Such statements are subject to certain risks and uncertainties, particularly those inherent in the process of developing and commercializing drugs,
including the adequacy of the Company's capital to support the Company's operations, the Company's ability to raise additional funds and the potential terms of such potential financing,
the timing and prospects for regulatory approval to market ADASUVE in Europe, Latin America, Russia and the Commonwealth of Independent States countries, the timing of the FDA's review of the resubmitted ADASUVE NDA and the eventual prospects that ADASUVE will be approved for marketing in the U.S. The Company's forward-looking statements also involve assumptions that, if they prove incorrect, would cause its results to differ materially from those expressed or implied by such forward-looking statements. These and other risks concerning Alexza's business are described in additional detail in the Company's Annual Report on Form 10-K for the year ended December 31, 2011 and the Company's other Periodic and Current Reports filed with the Securities and Exchange Commission. Forward-looking statements contained in this announcement are made as of this date, and the Company undertakes no obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise.
SOURCE Alexza Pharmaceuticals, Inc.