New Non-Profit Organization to Speed Pharmaceutical R&D
Ten leading biopharmaceutical companies announced today that they have
formed a non-profit organization to accelerate the development of new
medicines. Abbott, AstraZeneca, Boehringer Ingelheim, Bristol-Myers
Squibb, Eli Lilly and Company, GlaxoSmithKline, Johnson & Johnson,
Pfizer, Genentech a member of the Roche Group, and Sanofi launched TransCelerate
BioPharma Inc. (“TransCelerate”), the largest ever initiative of
its kind, to identify and solve common drug development challenges with
the end goals of improving the quality of clinical studies and bringing
new medicines to patients faster.
Through participation in TransCelerate, each of the ten
founding companies will combine financial and other resources, including
personnel, to solve industry-wide challenges in a collaborative
environment. Together, member companies have agreed to specific
outcome-oriented objectives and established guidelines for sharing
meaningful information and expertise to advance collaboration.
“There is widespread alignment among the heads of R&D at major
pharmaceutical companies that there is a critical need to substantially
increase the number of innovative new medicines, while eliminating
inefficiencies that drive up R&D costs,” said newly appointed acting CEO
of TransCelerate BioPharma, Garry Neil, MD, Partner at
Apple Tree Partners and formerly Corporate Vice President, Science &
Technology, Johnson & Johnson. “Our mission at TransCelerate
BioPharma is to work together across the global research and
development community and share research and solutions that will
simplify and accelerate the delivery of exciting new medicines for
patients.”
Members of TransCelerate have identified clinical study
execution as the initiative’s initial area of focus. Five projects have
been selected by the group for funding and development, including:
development of a shared user interface for investigator site portals,
mutual recognition of study site qualification and training, development
of risk-based site monitoring approach and standards, development of
clinical data standards, and establishment of a comparator drug supply
model.
As shared solutions in clinical research and other areas are developed, TransCelerate
will involve industry alliances including Clinical Data Interchange
Standards Consortium (CDISC), Critical-Path Institute (C-Path), Clinical
Trials Transformation Initiative (CTTI), Innovative Medicines Initiative
(IMI), regulatory bodies including the US Food and Drug Administration
(FDA) and European Medicines Agency (EMA), and Contract Research
Organizations (CROs).
Janet Woodcock, MD, director of FDA's Center for Drug Evaluation and
Research, said, “We applaud the companies in TransCelerate
BioPharma for joining forces to address a series of longstanding
challenges in new drug development. This collaborative approach in the
pre-competitive arena, utilizing the collective experience and resources
of 10 leading drug companies and others to follow, has the promise to
lead to new paradigms and cost savings in drug development, all of which
would strengthen the industry and its ability to develop innovative and
much-needed therapies for patients.”
"These leading pharmaceutical companies are in a position to
significantly influence changes in the way that clinical trials are
done, so that better answers about the benefits and risks of drugs and
other therapies are provided in a more efficient manner,” said Robert
Califf, MD, Co-Chair of CTTI and Director of the Duke Translational
Medicine Institute. “This initiative is complementary to efforts of
CTTI, and we look forward to working with TransCelerate BioPharma
to improve the conduct of clinical trials.”
TransCelerate BioPharma evolved from relationships
fostered via the Hever Group, a forum for executive R&D leadership to
discuss relevant issues facing the industry and solutions for addressing
common challenges. TransCelerate was incorporated in early
August 2012 and will file for non-profit status this fall. The Board of
Directors includes R&D heads of ten member companies. Membership in TransCelerate
is open to all pharmaceutical and biotechnology companies who can
contribute to and benefit from these shared solutions. TransCelerate’s
headquarters will be located in Philadelphia, PA.

Media:Porter NovelliVirginia Amann, 608-207-0082Virginia.Amann@PorterNovelli.comorShannon Caudill740-281-3715 or 614-378-9042Shannon.Caudill@PorterNovelli.com