Enzo Biochem Inc. (NYSE:ENZ) announced today that favorable results of
the Company’s clinical trial for treatment of non-alcoholic
steatohepatitis (NASH) were presented at the annual meeting of the
American Association for the Study of Liver Diseases. The study was a
randomized double blind placebo controlled format of EGS21, Enzo’s
orally administered beta glucosylceramide formulation, designed to
evaluate safety and efficacy of the study drug in patients with NASH and
its associated metabolic syndrome.
Enzo scientists and collaborators presented data showing that "oral
administration of EGS21 appears to be safe and biologically active in
patients with insulin resistance and NASH, leading to decreased hepatic
steatosis, and improved insulin resistance.”
Twenty one patients with biopsy proven NASH were enrolled and received
an oral dose of EGS21 or placebo daily during the 40-week study. The
patients were followed by measuring the effect of treatment on BMI (body
mass index), lipid profile, insulin sensitivity, HbA1c (glycated
hemoglobin) and glucose tolerance. Quantification of hepatic fat was
determined by MRI, and liver damage was assessed by a repeat liver
biopsy and measurement of liver enzymes. The immune modulatory effect of
EGS21 was determined by a measurement of circulatory immune cells, CD4,
CD8 and NKT cells.
No treatment-related adverse events were observed during treatment or
follow-up in any of the patients, they added.
Treatment with EGS21 was associated with an improvement in the metabolic
syndrome. Of the primary endpoints, HbA1c decreased by 0.1% compared
with a 0.09% in the placebo group. Of the secondary endpoints, glucose
tolerance improved in 50% of the patients compared with 38% of the
placebo group. HDL levels increased in 33% of the treated patients
compared with none in the placebo group. Patients treated with EGS21
showed a decrease in the hepatic fat score measured by MRI of 14%
compared to 7.7% in the placebo group, indicating a reduction in hepatic
steatosis. No significant change in liver enzymes was noted between the
two patient groups.
The observed changes were associated with changes in peripheral immune
cells. A 52% increase in peripheral NKT lymphocytes was observed
compared with a 74% decrease in the placebo group, and a 57% decrease in
the CD4/CD8 ratio of treated patients compared with a 138% increase in
patients who received placebo. These data support the role of immune
cell therapies in patients with insulin resistance and NASH.
EGS21 is a proprietary formulation of beta glucosylceramide, a naturally
occurring gylcosphingolipid that was shown to improve hepatic steatosis,
steatohepatitis and insulin resistance in animal models of non-alcoholic
fatty liver disease (NAFLD) by exerting an NKT regulatory lymphocyte
dependent immune modulatory effect.
NASH, or nonalcoholic fatty liver disease, is the most common form of
chronic liver disease in the Western world. NASH is one stage in a
disease spectrum that ranges from simple fatty liver or steatosis to
steatohepatitis, advanced fibrosis, and end-state cirrhosis. NASH
affects 2 to 5 percent of Americans and is becoming more common,
possibly because of the greater number of Americans with obesity,
according to The National Institute of Diabetes and Digestive and Kidney
Diseases.
The causes of NASH are not well defined, and currently there is no
effective medical therapy available.
"Study data support the role of NKT-based immunotherapies in patients
with insulin resistance and NASH, and is consistent with Enzo’s
pre-clinical and clinical studies involving the development of new
therapeutic platforms for immune mediated diseases,” said Elazar
Rabbani, Ph.D., Enzo Chairman and CEO.
About Enzo
Enzo Biochem is engaged in the research, development, manufacture and
licensing of innovative health care products and technologies based on
molecular biology and genetic engineering techniques, and in providing
diagnostic services to the medical community. Enzo’s Life Sciences
division develops, produces and markets proprietary labeling and
detection products for gene sequencing, genetic analysis and
immunological research among others. Its catalog of over 40,000
products serves the molecular biology, drug discovery and pathology
research markets. The Company's therapeutic division is in various
stages of clinical evaluation of its proprietary immune regulation
medicines for uveitis and Crohn's disease and conducts pre-clinical
research on several candidate compounds aimed at producing new mineral
and organic bone, including technology that could provide therapy for
osteoporosis and fractures, among other applications. Enzo’s Clinical
Labs division provides routine and esoteric reference laboratory
services for physicians in the New York Metropolitan and New Jersey
areas. Underpinning the Company’s technology and operations is an
extensive intellectual property estate in which Enzo owns or licenses
over 230 patents worldwide, and has pending applications for over 200
more. For more information visit the Company’s website www.enzo.com.
Except for historical information, the matters discussed in this news
release may be considered "forward-looking" statements within the
meaning of Section 27A of the Securities Act of 1933, as amended and
Section 21E of the Securities Exchange Act of 1934, as amended. Such
statements include declarations regarding the intent, belief or current
expectations of the Company and its management. Investors are cautioned
that any such forward-looking statements are not guarantees of future
performance and involve a number of risks and uncertainties that could
materially affect actual results. The Company disclaims any obligations
to update any forward-looking statement as a result of developments
occurring after the date of this press release.