Multiple Myeloma Research Foundation (MMRF) Celebrates the FDA Accelerated Approval of Pomalyst® (pomalidomide) for the

  Multiple Myeloma Research Foundation (MMRF) Celebrates the FDA Accelerated
  Approval of Pomalyst® (pomalidomide) for the Treatment of Relapsed and
  Refractory Multiple Myeloma

The MMRF and the Multiple Myeloma Research Consortium (MMRC) Provided Integral
         Support that Accelerated the Phase I and II Clinical Trials

Business Wire

NORWALK, Conn. -- February 8, 2013

The Multiple Myeloma Research Foundation (MMRF) today joined the multiple
myeloma community in celebrating the U.S. Food and Drug Administration’s (FDA)
decision to grant accelerated approval of Pomalyst^® (Celgene Corporation,
pomalidomide) for the treatment of patients with relapsed and refractory
multiple myeloma who no longer respond to currently available treatments. A
critical advance for the treatment of this incurable blood cancer, together
with Kyprolis^TM (carfilzomib), Pomalyst marks the second treatment to receive
accelerated approval in the last seven months, which is unparalleled in any
other cancer.

“Today marks another historic day - the availability of an unprecedented
second breakthrough therapy for this fatal disease within just seven months
for patients who have run out of treatment options,” stated Kathy Giusti,
Founder and CEO of the MMRF and the Multiple Myeloma Research Consortium
(MMRC), and a multiple myeloma patient. “We are grateful for the FDA’s
decision and for the unwavering commitment of our partner Celgene to the
multiple myeloma patient community, and are proud to have accelerated the
development of this promising new treatment.”

In 2008, the MMRC entered into collaboration with Celgene and bolstered the
clinical development of Pomalyst. Since that time, the MMRC:

  *Facilitated the Phase I and Phase II clinical trials that provided the
    basis for the accelerated approval, which included assistance with
    protocol development and Institutional Review Board (IRB) submissions.
  *Drove rapid patient enrollment to the Phase I and Phase II registration
    trials, enrolling 100% of patients in the Phase I trial and more than 80%
    in the Phase II trial, completing enrollment in less than two years and
    exceeding timeline expectations by several months.
  *Provided dedicated site management and guidance on key safety and efficacy
    issues throughout the Phase I and Phase II registration trials.
  *Supported further investigation of Pomalyst for multiple myeloma; to date,
    the MMRC has opened four trials involving pomalidomide, two of which are
    novel combinations that are currently open for enrollment.

Pomalyst was approved by the FDA for patients who have received at least two
prior therapies including Revlimid^® (lenalidomide) and Velcade^® (bortezomib)
and have demonstrated disease progression on or within 60 days of completion
of the last therapy, and will only be available in the United States through
POMALYST REMS™, a restricted distribution program.

About the Multiple Myeloma Research Foundation (MMRF)

The Multiple Myeloma Research Foundation (MMRF) was established in 1998 as a
501(c)(3) non-profit organization by twin sisters Karen Andrews and Kathy
Giusti, soon after Kathy's diagnosis with multiple myeloma. The mission of the
MMRF is to relentlessly pursue innovative means that accelerate the
development of next-generation multiple myeloma treatments to extend the lives
of patients and lead to a cure. As the world's number-one private funder of
multiple myeloma research, the MMRF has raised over $200 million since its
inception and directs 90% of total budget to research and related programming.
As a result, the MMRF has been awarded Charity Navigator’s coveted four-star
rating for nine consecutive years, the highest designation for outstanding
fiscal responsibility and exceptional efficiency. For more information about
the MMRF, please visit

About the Multiple Myeloma Research Consortium

The Multiple Myeloma Research Consortium (MMRC) is a 509(a)3 non-profit
organization that integrates leading academic institutions to accelerate drug
development in multiple myeloma. It is led from MMRC offices in Norwalk,
Conn., and comprises 16 member institutions: Barbara Ann Karmanos Cancer
Institute, Baylor Charles A. Sammons Cancer Center at Dallas, City of Hope,
Dana-Farber Cancer Institute, Emory University's Winship Cancer Institute, the
John Theurer Cancer Center at Hackensack University Medical Center, Mayo
Clinic, Mount Sinai School of Medicine, Ohio State University, Sarah Cannon
Research Institute, University Health Network (Princess Margaret Hospital),
University of California-San Francisco, University of Chicago, University of
Michigan, Virginia Cancer Specialists, and Washington University in St. Louis.

The MMRC is the only consortium to join academic institutions through
membership agreements, customized IT systems, and an integrated tissue bank.
For more information, please visit


Anne Quinn Young, 203-536-8691
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