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Trophos SA Receives Grant from The Michael J. Fox Foundation to
Evaluate Compounds in Parkinson's Disease Model
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Neurodegenerative disease specialist to collaborate with UCLA scientists
to test a new therapeutic approach in a preclinical model of Parkinson's disease
Marseille, February 8th, 2008 - Trophos SA, a biopharmaceutical company
specializing in the discovery and development of drugs for neurological
disorders, announces today that The Michael J. Fox Foundation (MJFF) has awarded
the company a Therapeutics Development Initiative grant to pursue the evaluation
of compounds preventing mitochondrial dysfunction to treat Parkinson's disease
(PD).
The project aims to establish the ability of two Trophos compounds to arrest or
prevent the early PD-like behavioral changes observed in a preclinical model
overexpressing human alpha-synuclein. Mutations in alpha-synuclein cause
familial PD and the protein accumulates in affected neurons in sporadic forms of
the disease. The model has been extensively studied by Marie-Françoise Chesselet,
MD, PhD, and her team at UCLA, who will conduct the project in collaboration
with Trophos. Dr. Chesselet is the Charles Markham Professor of Neurology at
UCLA and Chair of the Department of Neurobiology. She has an extensive
background in the basic science of neurological disorders and is a world expert
on the biology of central nervous system (CNS) diseases such as PD.
PD is caused by a broad pathology, including the death of brain dopaminergic
neurons that are essential for controlling movement. While the exact cause of PD
is not known, evidence suggests that mitochondrial malfunction occurs in
stressed dopaminergic neurons. Several environmental toxins that produce
symptoms remarkably like PD and several genes associated with familial PD lead
to mitochondrial malfunction. The team at UCLA has documented early PD-like
behavioral changes in the preclinical model overexpressing human alpha-synuclein.
Trophos has identified a family of compounds that enhance the survival of motor
neurons in models of motor neuron degeneration. These compounds bind to
mitochondrial proteins and thereby maintain mitochondrial function in cells
subjected to various types of stress. The two Trophos compounds to be studied
have been extensively characterized, and one of them, TRO19622, has already
demonstrated a very good safety profile in human clinical trials. Should either
compound show potential therapeutic benefit in the PD model, it could progress
to clinical testing in patients with PD.
"We are very pleased that Trophos has been awarded funding under the
Therapeutics Development Initiative for the preclinical evaluation of Trophos
compounds in the PD model," said Rebecca Pruss, CSO at Trophos. "Evidence that a
Trophos compound that targets mitochondria has a beneficial effect could
establish a new therapeutic approach to the treatment of PD and potentially
other neurodegenerative diseases."
"By funding industry partners directly, MJFF's TDI initiative helps us to
optimize and advance the most promising treatments that might otherwise get
stuck at the pre-clinical stage for lack of funding," said Katie Hood, CEO of
The Michael J. Fox Foundation. "The grant to Trophos is an excellent example of
how our capital, while comparatively modest, can serve as a 'carrot' to leverage
companies' expertise and infrastructure and speed the development of treatments
that could have an immense impact on patients' quality of life."
About Trophos: www.trophos.com
Trophos is a biopharmaceutical company committed to the discovery and
development of novel therapeutic compounds to treat neurological disorders and
other diseases with high unmet medical needs. The Trophos discovery strategy has
enabled it to develop a proprietary portfolio of products, such as our lead
product TRO19622 & drug candidate TRO40303, that confer a survival benefit upon
both neuronal and non-neuronal cells. This is achieved through a
mitochondria-based mechanism of action with a robust therapeutic rationale
predicted to exhibit a therapeutic benefit in diseases such as neuropathic pain,
ischemia-reperfusion injury and hepatotoxicity. The company is focusing its
efforts on the orphan indicates ALS, SMA and Huntington's disease, while seeking
to establish clinical proof of concept and partnerships in other indications,
such as PD. The company is currently performing two clinical studies with
TRO19622, a Phase IIa trial in painful diabetic neuropathy and a Phase Ib study
in SMA.
Trophos was founded in 1999, is based in Marseille, France and currently has 32
employees.
About the Michael J. Fox Foundation:
www.michaeljfox.org
Founded in 2000, The Michael J. Fox Foundation for Parkinson's Research is
dedicated to ensuring the development of a cure for Parkinson's disease within
this decade through an aggressively funded research agenda. The Foundation has
funded over (USD) 115 million in research to date.
For further information, please contact:
Andrew Lloyd & Associates
Andrew Lloyd / Neil Hunter
Tel: +44 1273 675100
allo@ala.com /
neil@ala.com
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