Contact Information: Contact: Rachel Levine Director Corporate Development & Communications Cleveland BioLabs, Inc. T: (646) 284-9439 E: rlevine@cbiolabs.com
Cleveland BioLabs Receives First U.S. Patent for Radiation Protection Drug CBLB502
| Source: Cleveland BioLabs, Inc.
BUFFALO, NY--(Marketwire - January 6, 2010) - Cleveland BioLabs, Inc. (NASDAQ : CBLI )
announced today that the U.S. Patent and Trademark Office has issued US
Patent No. 7,638,485 titled "Modulating Apoptosis" covering the method of
protecting a mammal from radiation using flagellin or its derivatives,
including CBLB502. This patent was already granted by the nine member
countries of the Eurasian Patent Organization (EAPO), and two additional
nations.
Cleveland BioLabs has also filed two additional new patent applications
related to Protectan technology in the U.S. around various aspects and
properties for CBLB502 and related Protectan compounds, including new
methods of use of flagellin derivatives and screening for new compounds
with similar properties.
Yakov Kogan, Ph.D., MBA, Chief Operating Officer of Cleveland BioLabs,
noted, "With more than 13 sets of patents filed to date in the U.S. and
internationally around various properties of CBLB502 and related compounds,
we believe we have protected the potentially broad uses of our Protectan
technology. The receipt of our first U.S. patent for protection from
radiation is a major milestone in our development of CBLB502 and we
continue to advance our work in this and other areas of protection from
acute stresses."
About CBLB502
CBLB502 is a derivative of a microbial protein, which has demonstrated the
capacity to reduce injury from acute stresses, such as radiation in animal
models. CBLB502 mobilizes several cell protective mechanisms, including
inhibition of programmed cell death (apoptosis), reduction of oxidative
damage and induction of regeneration-promoting cytokines.
CBLB502 is being developed under the U.S. Food and Drug Administration's
Animal Efficacy Rule to treat Acute Radiation Syndrome (ARS) or radiation
poisoning from any exposure to radiation such as a nuclear or radiological
weapon/ dirty bomb, or from a nuclear accident. This approval pathway
requires demonstration of efficacy in representative animal models and
safety and drug metabolism testing in healthy human volunteers.
Evidence of CBLB502's mechanism of action and activity in animal models was
published in Science Magazine in April 2008 (Science, 2008, vol. 320, pp.
226-230). Data from 50 subjects in an initial Phase I safety and
tolerability study indicated that CBLB502 was well tolerated and that
normalized biomarker results corresponded to previously demonstrated
activity in animal models of ARS. There is currently no FDA approved
medical countermeasure to treat ARS.
CBLB502 is also being developed as a supportive care measure to reduce and
prevent occurrence of side effects of radiotherapy or chemotherapy in
cancer treatment.
About Cleveland BioLabs, Inc.
Cleveland BioLabs, Inc. is a drug discovery and development company
leveraging its proprietary discoveries around programmed cell death to
develop treatments for cancer and protection of normal tissues from
exposure to radiation and other stresses. The Company has strategic
partnerships with the Cleveland Clinic, Roswell Park Cancer Institute,
ChemBridge Corporation and the Armed Forces Radiobiology Research
Institute. To learn more about Cleveland BioLabs, Inc., please visit the
company's website at http://www.cbiolabs.com.
This press release contains forward-looking statements within the meaning
of the Private Securities Litigation Reform Act of 1995. Forward-looking
statements reflect management's current expectations, as of the date of
this press release, and involve certain risks and uncertainties. The
Company's actual results could differ materially from those anticipated in
these forward-looking statements as a result of various factors. Some of
the factors that could cause future results to materially differ from the
recent results or those projected in forward-looking statements include the
"Risk Factors" described in the Company's periodic filings with the
Securities and Exchange Commission.