Pharsight Launches PK Accelerator(TM)
June 24 2008 - 5:30AM
PR Newswire (US)
PK Accelerator Bundled Solution Accelerates Pharmacokinetic
Analysis and Reporting MOUNTAIN VIEW, Calif., June 24
/PRNewswire-FirstCall/ -- Pharsight Corporation (NASDAQ:PHST), a
leading provider of software, strategic consulting, and regulatory
services for optimizing clinical drug development, today announced
that it will be launching PK Accelerator (PKA(TM)), a system of
bundled software coupled with a rapid deployment service provided
at a fixed price and fixed scope. Adopting PK Accelerator will
allow small to mid-sized organizations to deploy Pharsight's "best
practices" solution for end-to-end pharmacokinetic analysis and
validatable CFR 21 part 11 reporting in as little as 90 days. Small
to mid-sized research oriented pharmaceutical and biotech companies
deploying PK Accelerator will be able to take advantage of the
operational efficiencies Pharsight's enterprise and desktop
software packages were designed to deliver. The software components
of the PKA bundle will consist of the Pharsight(R) Knowledgebase
Server(TM) (PKS), WinNonlin(R) Autopilot(TM), PKS Reporter(TM), the
PKS and WinNonlin Validation Suites(TM), upgrades to WinNonlin
Enterprise, and a choice of two of the following database
connectors: Watson(TM), Excel(TM), or CDISC. All of these
components have been designed for seamless interoperability and
will be implemented as a complete system with minimal
configuration. PK Accelerator will bring state-of-the-art clinical
pharmacology archiving, analysis, and reporting capabilities within
reach of smaller firms by standardizing the system's training and
deployment procedures and leveraging Pharsight's best practices
recommendations for system configuration and implementation.
Standardized connector settings and transformations, standardized
validation scripts, standardized software settings, standardized
analysis and reporting templates and standardized business rules
will all work together to improve the ROI for Pharsight's PK
accelerating technologies. "PK Accelerator allows you to integrate
data into standardized PK-ready analysis formats, perform the
analysis, and generate final NCA reports in as little as a day,"
said Shawn O'Connor, president, chief executive officer and
chairman of Pharsight. "Pharsight is leveraging its lessons learned
on 22 previous PKS and numerous AutoPilot and Reporter deployments
and streamlining the process in order to accommodate the needs of
small to mid-sized pharma and biotech companies." About PKS
Pharsight(R) Knowledgebase Server(TM) (PKS) is a high-productivity,
regulatory-compliant enterprise data repository that manages
modeling and simulation data. PKS enables pharmaceutical and
biotechnology companies to better manage and control preclinical
and clinical PK/PD data and analyses, thus supporting higher
modeling productivity as called for in the FDA's Critical Path
Initiative. Companies also use PKS to build PK/PD data management
architecture that complies with the FDA's regulation 21 CFR Part
11, which has set new standards for computer system validation and
usage. PKS is directly integrated with WinNonlin Enterprise,
Pharsight's industry-leading PK/PD modeling and analysis tool, for
state-of-the-art modeling and analyses, and supports direct access
to any ODBC-capable data source. PKS also supports analysis with
leading tools such as NONMEM(R), and SAS(R), and data import from
leading clinical data management and laboratory information
management systems such as Watson LIMS(TM). PKS software is
designed to complement other Pharsight products, including Trial
Simulator(TM) and Drug Model Explorer(R) (DMX(R)), which are used
for computer-based drug-disease modeling, clinical trial
simulation, and drug model visualization. About WinNonlin AutoPilot
WinNonlin(R) AutoPilot(TM) orchestrates PK analyses by selecting
input data from a user's local file system or Pharsight
Knowledgebase Server(TM) ("PKS"), and then directs WinNonlin to
perform analyses and produce report quality tables, figures, and
text output (e.g., in Microsoft(R) Excel(TM), SigmaPlot(R), and
Microsoft Word(TM)) for regulatory submissions and interim reports.
Formatted PK analyses outputs must reflect the requirements and
SOPs of each research organization, and WinNonlin AutoPilot
provides a user interface that allows extensive configuration of
formatting and business rules to enable clear communication of
standards and immediate use across the organization. PK analyses
that can be automated include noncompartmental analysis for
different study designs and inferential statistics (e.g.,
bioequivalence testing), as well as comparisons between analytes,
dose routes or other conditions. Used in conjunction with PKS and
PKS Reporter(TM), WinNonlin AutoPilot provides standardized,
regulatory compliant, secure and automatic generation of routine
analyses and reports. Used independently of PKS and PKS Reporter,
WinNonlin AutoPilot can provide significant return on investment
through productivity gains and quality improvements in PK analysis
and reporting. About PKS Reporter PKS Reporter(TM) addresses the
need for streamlined, systematic, and automated report generation
and signature. Using PKS as an underlying source of secure,
regulatory-compliant report content, PKS Reporter allows
researchers to use familiar tools such as WinNonlin and Microsoft
Word(R) to construct, update, review and approve any type of
report. About WinNonlin Validation Suite The WinNonlin Validation
Suite(TM) streamlines your on-site validation of the WinNonlin
product. The Validation Suite provides a selection of automated
tests, each of which runs a specific WinNonlin analysis or function
and tests the results against standardized, known output. About PKS
Validation Suite The PKS Validation Suite(TM) streamlines your
on-site validation of the PKS product. The Validation Suite
provides document templates, test data, and a collection of
automated and manual test scripts. Leveraging the PKS Validation
Suite as a starting point for validation efforts can save months of
planning, testing, and reporting time. About Pharsight Corporation
Pharsight(R) Corporation develops and markets integrated products
and services that enable pharmaceutical and biotechnology companies
to achieve significant and enduring improvements in the development
and use of therapeutic products. The company's goal is to help
customers reduce the time, cost and risk of drug development, as
well as optimize the post-approval marketing and use of
pharmaceutical products. Pharsight's approach enhances the
fundamental element of drug development success: strong
decision-making. By adopting the Pharsight approach, customers
acquire a new decision-making process with the potential to
systematically improve every level and phase of their business and
scientific processes. Pharsight is headquartered in Mountain View,
California. Information about Pharsight is available at
http://www.pharsight.com/. Forward-Looking Statements The
statements in this press release related to the functionality,
performance, and benefits of the PK Accelerator(TM) bundled
software are forward-looking statements. Forward-looking statements
are inherently speculative, and the actual results and customer's
experience may differ materially from Pharsight's expectations due
to a variety of factors, including: changes in FDA regulations and
customers may not perceive the benefits of the IVIVC Toolkit(TM)
for WinNonlin(R) to be the same as Pharsight believes them to be.
Other risk factors relating to Pharsight are disclosed in the
company's most recent Form 10-Q filed with the Securities and
Exchange Commission on February 14, 2008. All forward-looking
statements are based on information available to the company on the
date hereof, and the company assumes no obligation to update such
statements. Registered Trademarks and Trademarks Pharsight is a
registered trademark of Pharsight Corporation. All other brand and
product names are trademarks or registered trademarks of their
respective holders. DATASOURCE: Pharsight Corporation CONTACT:
investors, Douglas Sherk or Matthew Selinger, +1-415-896-6820, or
media, Steve DiMattia or Donald Takaya, +1-646-201-5445, all of EVC
Group, for Pharsight Corporation Web site:
http://www.pharsight.com/
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