Genzyme to Provide $900,000 Grant to University of Florida Researcher

Company Website:
http://www.genzyme.com
CAMBRIDGE, Mass. -- (Business Wire)
Genzyme,
a Sanofi company (EURONEXT: SAN and NYSE: SNY), today announced the
establishment of a research collaboration with the University of Florida
and the University of Pennsylvania to develop a gene therapy for the
treatment of a rare genetic disease that causes childhood blindness.
Leber congenital amaurosis type 1 (LCA-1) is usually diagnosed in
children who are less than a year old, and patients remain severely
visually impaired for the rest of their lives.
Genzyme is providing $900,000 in funding over three years to Dr. Shannon
Boye, assistant professor of ophthalmology at the University of Florida,
to fund her LCA-1 research. Dr. Boye’s research is focused on a gene
called guanylate cyclase (GUCY2D) that is mutated in LCA-1
patients. The GUCY2D gene normally makes GC1, a protein expressed
in photoreceptors, which are located in the retina of the eye and
convert light into electrical signals that the brain interprets as
vision. Genzyme’s funding supplements current funding from the
Foundation Fighting Blindness.
The majority of the early stage LCA-1 research is being conducted at the
University of Florida, with Genzyme taking on increasingly more
activities as the program advances toward clinical trials. Genzyme has
the option to in-license the potential treatment before it enters
clinical trials.
“Genzyme is a very collaborative partner and has been wonderful to work
with,” said Dr. Boye. “We share a heartfelt commitment to helping LCA-1
patients and their families and to pursuing a treatment building upon
prior, promising non-clinical studies.”
The gene therapy is administered by inserting a healthy copy of the GUCY2D
gene into the eye. The healthy gene is put into an adeno associated
viral (AAV) vector whose viral DNA has already been removed. The viral
vector is injected into the retina and transfers the healthy gene to the
photoreceptors, with the goal of treating the disease with a single
treatment.
“This research is both very promising and very important,” said Abraham
Scaria, Senior Scientific Director and Project Leader for the LCA-1
program. “We are excited by the prospect of what this treatment would
mean for children diagnosed with this disease.”
Treating physicians of LCA-1 patients from the University of
Pennsylvania are also playing a key role in this research. They provide
information to the University of Florida and Genzyme about indicators to
look for in trials to know whether or not the therapy is working. They
are also conducting a natural history study, which tracks how the retina
of an LCA-1 patient progresses over time if untreated.
“We are proud to partner with Dr. Shannon Boye and her team at the
University of Florida, who are leading experts in the field of ocular
gene therapy, as well as our clinical colleagues from the University of
Pennsylvania, who are sharing important insights about LCA-1 patients’
needs,” said Rich Gregory, Ph.D., Head of the Sanofi Genzyme R&D Center.
“Together, we are striving to provide new hope to children who might not
otherwise be able to see.”
About Genzyme, a Sanofi Company
Genzyme has pioneered the development and delivery of transformative
therapies for patients affected by rare and debilitating diseases for
over 30 years. We accomplish our goals through world-class research and
with the compassion and commitment of our employees. With a focus on
rare diseases and multiple sclerosis, we are dedicated to making a
positive impact on the lives of the patients and families we serve. That
goal guides and inspires us every day. Genzyme’s portfolio of
transformative therapies, which are marketed in countries around the
world, represents groundbreaking and life-saving advances in medicine.
As a Sanofi company, Genzyme benefits from the reach and resources of
one of the world’s largest pharmaceutical companies, with a shared
commitment to improving the lives of patients. Learn more at www.genzyme.com.
About Sanofi
Sanofi, a global and diversified healthcare leader, discovers, develops
and distributes therapeutic solutions focused on patients’ needs. Sanofi
has core strengths in the field of healthcare with seven growth
platforms: diabetes solutions, human vaccines, innovative drugs,
consumer healthcare, emerging markets, animal health and the new
Genzyme. Sanofi is listed in Paris (EURONEXT: SAN) and in New York
(NYSE: SNY).
Forward Looking Statements
This press release contains forward-looking statements as defined in
the Private Securities Litigation Reform Act of 1995, as amended.
Forward-looking statements are statements that are not historical facts.
These statements include projections and estimates and their underlying
assumptions, statements regarding plans, objectives, intentions and
expectations with respect to future financial results, events,
operations, services, product development and potential, and statements
regarding future performance. Forward-looking statements are generally
identified by the words “expects”, “anticipates”, “believes”, “intends”,
“estimates”, “plans” and similar expressions. Although Sanofi’s
management believes that the expectations reflected in such
forward-looking statements are reasonable, investors are cautioned that
forward-looking information and statements are subject to various risks
and uncertainties, many of which are difficult to predict and generally
beyond the control of Sanofi, that could cause actual results and
developments to differ materially from those expressed in, or implied or
projected by, the forward-looking information and statements. These
risks and uncertainties include among other things, the uncertainties
inherent in research and development, future clinical data and analysis,
including post marketing, decisions by regulatory authorities, such as
the FDA or the EMA, regarding whether and when to approve any drug,
device or biological application that may be filed for any such product
candidates as well as their decisions regarding labelling and other
matters that could affect the availability or commercial potential of
such product candidates, the absence of guarantee that the product
candidates if approved will be commercially successful, the future
approval and commercial success of therapeutic alternatives, the Group’s
ability to benefit from external growth opportunities, trends in
exchange rates and prevailing interest rates, the impact of cost
containment policies and subsequent changes thereto, the average number
of shares outstanding as well as those discussed or identified in the
public filings with the SEC and the AMF made by Sanofi, including those
listed under “Risk Factors” and “Cautionary Statement Regarding
Forward-Looking Statements” in Sanofi’s annual report on Form 20-F for
the year ended December 31, 2013. Other than as required by applicable
law, Sanofi does not undertake any obligation to update or revise any
forward-looking information or statements.

Contacts:
Genzyme
Lori Gorski, 617-768-9344
Lori.Gorski@genzyme.com
Source: Genzyme
© 2026 Canjex Publishing Ltd. All rights reserved.