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Monogram Announces HERmark(TM) Oral Presentation at the 44th ASCO Annual Meeting
Monogram Announces HERmark(TM) Oral Presentation at the 44th ASCO Annual Meeting
SOUTH SAN FRANCISCO, Calif., May 16 /PRNewswire-FirstCall/ -- Monogram
Biosciences, Inc. (Nasdaq: MGRM) today announced that scientific collaborators
will present results on HERmark(TM), the company's novel oncology assay, as a
means to measure HER2 and predict response to Herceptin(R) (trastuzumab) in
patients with metastatic breast cancer at the upcoming 44th ASCO Annual
Meeting taking place inChicago, Illinois.
The oral presentation, entitled "Total HER2 and HER2 Homodimer Levels
Predict Response to trastuzumab", which will take place on Monday, June 2,
2008 from 1:15PM - 2:45PM, will discuss the findings of a study that
investigated the HERmark assay's ability to identify and discriminate among
patients with metastatic breast cancer who experienced different degrees of
response to trastuzumab. The results of the study, by Allan Lipton, M.D. and
colleagues at the Experimental Oncology Research Lab at Penn State/Hershey
Medical Center will be presented by Kim Leitzel, M.Sc., Senior Research
Associate in Dr. Lipton's laboratory.
"Current testing methods for determination of the likelihood of benefit
from Herceptin are not adequate," said Allan Lipton M.D., Professor of
Medicine & Oncology at Hershey Medical Center/Penn State University. "HERmark
represents a promising new technology that could provide enhanced information
on which patient therapy decisions may be based."
"HERmark is the first diagnostic built upon our VeraTag technology," said
Monogram CEO Bill Young. "We believe HERmark represents an advance in the
field by providing very reproducible quantitative measures of HER2 protein
expression levels and, for the first time, measurements of HER2 homodimers.
We believe these measurements will make the selection of patients for
Herceptin therapy more precise, as well as provide quantitative tools for the
ongoing investigation of HER2 biology in clinical specimens."
The study used Monogram's proprietary HERmark assay to analyze tissue
samples from patients with metastatic breast cancer who were treated with
Herceptin. Patients had been previously selected for Herceptin therapy by IHC
or FISH testing. Using HERmark to measure total HER2 and HER2 homodimer
levels, the results were compared with the patients' response to treatment
with Herceptin.
While current testing methods identified all these patients as being
equally likely to respond to Herceptin treatment, Monogram's HERmark assay was
able to distinguish separate sub-groups of patients with different clinical
outcomes, and those outcomes correlated with the quantitative measurements of
HER2 status provided by HERmark.
Patients with higher levels of HER2 and HER2 homodimers correlated with a
higher probability of objective response (an endpoint in tumor evaluation) to
Herceptin therapy. In addition, those patients with higher HER2 expression
levels had a median time to progression of 11.6 months while those in the
lower half of the distribution had a median time to progression of 5.4 months.
This was also true of patients with higher levels of HER2 homodimers who had a
median time to progression of 11.6 months compared to those with lower HER2
levels who had a median time to progression of 5.8 months. Further analysis
revealed that there was a trend in favor of higher HER2 expression and longer
overall survival (median survival 37.4 months vs. 28.7 months) although this
was not statistically significant (p=0.2). Finally, Cox multivariate analyses
identified HER2 expression and HER2 homodimer levels as independent correlates
of both time to progression and overall survival.
About HERmark
HERmark is a proprietary diagnostic that accurately quantifies HER2
expression and dimerization in patients with breast cancer. Preliminary data
from three cohorts of Herceptin-treated patients with metastatic breast cancer
who were identified as "HER2 positive" by conventional assays suggest that
HERmark can identify patients who are likely to respond to Herceptin with
greater precision than currently available tests, permitting stratification of
patients according to their degree of clinical benefit from the drug.
Additional studies of HERmark for breast cancer in both the metastatic and
adjuvant settings are in progress.
About VeraTag
VeraTag is a proximity-based assay technology platform that accurately
quantifies proteins and functional protein complexes. This platform provides a
researcher or clinician a more thorough understanding of protein-protein
interactions or signaling pathway activity allowing for disease
characterization at the molecular level. VeraTag is designed to run on
standard formalin-fixed paraffin embedded (FFPE) patient samples.
About Monogram
Monogram is advancing individualized medicine by discovering, developing
and marketing innovative products to guide and improve treatment of serious
infectious diseases and cancer. The Company's products are designed to help
doctors optimize treatment regimens for their patients that lead to better
outcomes and reduced costs. The Company's technology is also being used by
numerous biopharmaceutical companies to develop new and improved anti-viral
therapeutics and vaccines as well as targeted cancer therapeutics. More
information about the Company and its technology can be found on its web site
at http://www.monogrambio.com.
Forward Looking Statements
Certain statements in this press release are forward-looking. These
forward-looking statements include references to, the ability of VeraTag
technology and the HERmark assay to predict response to Herceptin or to
significantly improve the information available to physicians, results of
studies intended to demonstrate clinical utility of HERmark, and potential
commercialization of the HERmark assay. These forward-looking statements are
subject to risks and uncertainties and other factors, which may cause actual
results to differ materially from the anticipated results or other
expectations expressed in such forward-looking statements. These risks and
uncertainties include, but are not limited to: risks and uncertainties
relating to the performance of our products, including HERmark; the growth in
revenues; the risk that our VeraTag assays, including HERmark may not predict
response to Herceptin or other therapeutic agents; the risk that we may not be
able to obtain additional cohorts of patient samples for additional VeraTag
studies, our ability to successfully conduct clinical studies and the results
obtained from those studies; whether larger confirmatory clinical studies will
confirm the results of initial studies; our ability to establish reliable,
high-volume operations at commercially reasonable costs; actual market
acceptance of our products for patient use and adoption of our technological
approach and products by pharmaceutical and biotechnology companies; our
estimate of the size of our markets; our estimates of the levels of demand for
our products; the impact of competition; whether payers will authorize
reimbursement for our products and services and the amount of such
reimbursement that may be allowed; whether the FDA or any other agency will
decide to further regulate our products or services; whether the draft
guidance on Multivariate Index Assays issued by FDA will be subsequently
determined to apply to our current or planned products; whether we will
encounter problems or delays in automating our processes; the ultimate
validity and enforceability of our patent applications and patents; the
possible infringement of the intellectual property of others; whether licenses
to third party technology will be available; whether we are able to build
brand loyalty and expand revenues; restrictions on the conduct of our business
imposed by the Pfizer, Merrill Lynch and other debt agreements; the impact of
additional dilution if our convertible debt is converted to equity; and
whether we will be able to raise sufficient capital in the future, if
required. For a discussion of other factors that may cause actual events to
differ from those projected, please refer to our most recent annual report on
Form 10-K and quarterly reports on Form 10-Q, as well as other subsequent
filings with the Securities and Exchange Commission. We do not undertake, and
specifically disclaim any obligation, to revise any forward-looking statements
to reflect the occurrence of anticipated or unanticipated events or
circumstances after the date of such statements.
VeraTag and HERmark are trademarks of Monogram Biosciences, Inc.
Herceptin is a registered trademark of Genentech, Inc.
Contacts: Alfred G. Merriweather Jeremiah Hall
Chief Financial Officer Feinstein Kean Healthcare
Tel: 650 624-4576 Tel: 415 677-2700
amerriweather@monogrambio.com jeremiah.hall@fkhealth.com
SOURCE Monogram Biosciences, Inc.
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Copyright © 2008, NewsBlaze,
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