• Second indication
for Galapagos candidate drug G100192
• Sponsored by Charley’s Fund and Nash Avery
Foundation
• Initiation of preclinical development
Mechelen, Belgium
and Great Barrington, Massachusetts, USA; 17 September 2009
– Galapagos NV (Euronext: GLPG), Charley’s Fund
Inc. and the Nash Avery Foundation announced today that
they will collaborate to investigate the potential effectiveness
of Galapagos’ SARM candidate drug, G100192, in treating
Duchenne muscular dystrophy. G100192 is an orally-available
small molecule therapeutic, which has demonstrated successful
Proof of Concept in pre-clinical studies for cachexia (the
loss of weight and muscle mass).
Charley’s Fund and
the Nash Avery Foundation will support the costs of pre-clinical
studies to assess the potential effectiveness of G100192
in treating Duchenne muscular dystrophy. While investigating
this new indication, Galapagos will continue to develop
the SARM therapeutic for cachexia, and plans to initiate
a Phase I clinical trial in healthy volunteers in the beginning
of 2010.
“Working with Charley’s
Fund, the Nash Avery Foundation and experts in the field
of Duchenne gives us the opportunity to explore a second
indication for G100192 and expand the potential therapeutic
benefit of this candidate drug,” said Onno van de
Stolpe, CEO of Galapagos.
“The SARM therapeutic
that Galapagos is developing for cachexia could be of potential
benefit in treating Duchenne muscular dystrophy,”
said Benjamin Seckler, M.D., President of Charley’s
Fund. “If the pre-clinical models show efficacy in
treating this disease, G100192 could become one of the first
small molecule candidate drugs for Duchenne - complementing
the gene therapy and biologic approaches in development.”
About Duchenne muscular
dystrophy
Duchenne muscular dystrophy is the most common fatal genetic
disorder to affect children around the world. Approximately
one in every 3,500 boys worldwide is afflicted with Duchenne
muscular dystrophy with 20,000 new cases reported each year.
It is a devastating and incurable muscle-wasting disease
associated with specific inborn errors in the gene that
codes for dystrophin, a protein that plays a key structural
role in muscle fiber function. Symptoms usually appear in
male children before age six. Progressive muscle weakness
of the legs and pelvis eventually spreads to the arms, neck,
and other areas. By age 10, braces may be required for walking,
and most patients are confined to a wheelchair by age 12.
Eventually, this progresses to complete paralysis and increasing
difficulty in breathing. The condition is terminal and death
usually occurs before the age of 30. The outpatient cost
of care for a non-ambulatory Duchenne muscular dystrophy
patient is among the highest of any disease. There is currently
no cure for Duchenne muscular dystrophy, but for the first
time in decades, there are promising therapies in or moving
into development.
About Charley’s Fund
Charley’s Fund Inc. is a not-for-profit foundation
that finances therapeutics development for Duchenne muscular
dystrophy. The foundation’s mission is to expedite
a treatment or cure in time to help this generation of children
who suffer from Duchenne muscular dystrophy. Charley’s
Fund Inc. targets translational research — research
that moves science from the lab into human clinical trials.
The 501 (c)(3) public charity was co-founded in 2004 by
Benjamin Seckler, M.D. and Tracy Kramer Seckler, whose son
Charley has Duchenne muscular dystrophy. More info at: www.charleysfund.org.
About Nash Avery
Foundation
The Nash Avery Foundation is a not-for-profit private foundation
that is focused on financially supporting programs that
will slow and eventually stop Duchenne muscular dystrophy.
Nash Avery Foundation was founded by Angela and Tom Wicka
after their son Nash was diagnosed with DMD. The Foundation
believes that the solution in stopping this disease will
come from a combination of well funded science and getting
talented people focused on this disease. More info at: www.nashaveryfoundation.org.
About Galapagos
Galapagos (Euronext: GLPG; OTC: GLPYY) is a drug discovery
and development company with small molecule programs in
bone and joint diseases, bone metastasis, cachexia, anti-infectives
and metabolic diseases. It has established risk sharing
alliances with GSK, Janssen Pharmaceutica, Eli Lilly and
Merck and Co. Through an alliance with MorphoSys, Galapagos
is also developing new antibody therapies in bone and joint
diseases. Its division BioFocus DPI offers a full suite
of target-to-drug discovery products and services to pharmaceutical
and biotech companies and to patient foundations, encompassing
target discovery and validation, screening and drug discovery
through to delivery of pre-clinical candidates. Galapagos
currently employs 495 people and operates facilities in
six countries, with global headquarters in Mechelen, Belgium.
More info at: www.glpg.com.
CONTACTS
Galapagos NV
Onno van de Stolpe, CEO
Tel: +31 6 2909 8028
ir@glpg.com
Charley’s Fund Inc.
Benjamin D. Seckler, M.D., President
Tel: +1 413 528 5744 or +1 877 436 3363 (877-4-END-DMD)
info@charleysfund.org
Nash Avery Foundation
Tom C. Wicka, President and Founder
tom.wicka@iwco.com
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