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Quintiles Creates Strategic Biostatistics Unit to Help Sponsors Reduce Time, Costs of Clinical Drug Development

    New unit concentrates expertise in adaptive design, other innovative
                           statistical approaches

    RESEARCH TRIANGLE PARK, N.C., July 24 /PRNewswire/ -- Quintiles
Transnational Corp. today announced the creation of the Strategic
Biostatistics Unit to help customers cut the time and reduce the costs of
drug development through the "adaptive design" of clinical trials and other
innovative statistical approaches.
    A study design is called "adaptive" if it allows modification of an
essential design feature (e.g., sample size, randomization ratio, number of
treatment arms), based on accruing data from within that clinical trial,
with the possible adaptations fully pre-specified for confirmatory trials,
and in all cases carried out without compromising the integrity of the
trial.
    "The FDA's Critical Path Initiative highlights adaptive design as one
way to reduce the time and costs of clinical drug development while
retaining the ability to reach good statistical decisions," said Stephen C.
Smeach, Ph.D., Senior Vice President, Global Biostatistics & Medical
Writing, Quintiles. "We're at the cutting edge with respect to adaptive
design, both for Phase III and for Phase IIB-III trials. The FDA's
facilitation of adaptive design methodology could in many cases lead to
getting new medicines to patients faster and at less cost."
    "Quintiles has already developed or implemented at least 10 adaptive
designs within the last few years," said Jonathan R. Smith, Ph.D., Vice
President, Strategic Biostatistics Unit, incorporating one or more of the
following elements:
     - Sample size reassessment, e.g., to compensate for variability larger
       than anticipated and thus improving the chances of a statistically
       successful trial;
     - Combination of the Phase IIB dose selection stage with the Phase III
       confirmatory stage to produce a seamless Phase IIB-III trial, which can
       save substantial development time;
     - Bayesian adaptive design features that can save time and cost by
       incorporating data from earlier trials (or from earlier stages of the
       current trial).
    Quintiles also has developed or implemented many traditional group-
sequential designs that incorporate:
     - Stopping a clinical trial for futility, to cut costs when there is
       little chance that a statistically significant result can be obtained;
     - Stopping for early demonstration of efficacy, which can save both time
       and cost.
    The members of the Strategic Biostatistics Unit (Smith; Jorgen Seldrup,
Ph.D.; Michael O'Kelly, Ph.D.; and Zoran Antonijevic), based in the U.S.
and in Europe, have an average of more than 20 years of experience and
provide input to sponsors on innovative statistical approaches to cut time,
decrease costs or increase chance of success for individual studies or for
whole programs. The group also provides a corresponding service for
Quintiles' strategic investment unit, NovaQuest.
    About Quintiles
    Quintiles is the global leader in pharmaceutical services, improving
healthcare worldwide by providing innovative, quality professional
expertise, market intelligence and partnering solutions to meet the dynamic
needs of the pharmaceutical, biotechnology and healthcare industries.
Quintiles has 16,000 specialized employees and offices in more than 50
countries. For more information visit the company's Web site at
http://www.quintiles.com.


SOURCE Quintiles Transnational Corp.




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    CONTACT:
    Dick Jones, Media Relations, +1-919-998-2091,
    or media.info@quintiles.com, or Greg Connors, Investor Relations,
    +1-919-998-2000, or invest@quintiles.com , both of Quintiles
    Transnational Corp.