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Can-Fite BioPharma Signed a Cooperative Research and Development Agreement (CRADA) with the U.S. National Institute of Health (NIH).


PETACH TIKVA, Israel -- Can-Fite BioPharma (TASE TASE Tel Aviv Stock Exchange
TASE The All Seeing Eye
TASE Tactical Air Support Element
TASE Thrust Assessment Support Environment
TASE Telecontrol Application Service Elements (IEC communications protocol) 
:CFBI CFBI California Family Business Institute, LLC
CFBI Center for Functional Brain Imaging
) announced today on the signing of a Cooperative Research and Development Agreement “CRADA” redirects here. For other uses, see CRADA (disambiguation).

A Cooperative Research and Development Agreement (CRADA) is an agreement between a government agency and a private company to work together.
 (CRADA CRADA Cooperative Research And Development Agreement ) with the National Institute of Health in the U.S. The CRADA relates to new small molecules that are agonists of the A(3) adenosine receptor (A(3)AR), invented in the laboratory of Prof. Kenneth A. Jacobson from the NIH "Not invented here." See digispeak.

NIH - The United States National Institutes of Health.
. The A(3)AR is the prime target of Can-Fite's drug development efforts. The focus of the CRADA will be to identify such agonists with potential therapeutic use in the treatment of autoimmune inflammatory diseases and cancer.

Prof. Jacobson is a world renowned medicinal chemist with interests in the structure and pharmacology of receptors and in developing drugs that interact with G protein-coupled receptors (GPCRs), to which the A(3)AR belongs. He is a leading scientist in research relating to the A(3)AR and devoted much of his research to these receptors and to the synthesis of molecules that interact with them. He was the first scientist to synthesize agonists and antagonists to this receptor. One such agonist is CF101, Can-Fite's lead drug that was exclusively licensed by Can-Fite from the NIH and is scheduled to enter Phase IIb clinical studies in the 2nd quarter of 2006.

The CRADA will provide the company with a unique access to a new class of small molecule agonists to the A(3)AR that emerge from Prof. Jacobson's laboratory and hence with the ability to enrich its pipeline of small molecule drugs. Prof. Pnina Fishman, Can-Fite's CEO (1) (Chief Executive Officer) The highest individual in command of an organization. Typically the president of the company, the CEO reports to the Chairman of the Board.  indicated that she and the Can-Fite team are very pleased to collaborate with a scientist and a research institute of this caliber and stated her confidence that the CRADA will bear fruits that will be very beneficial to Can-Fite.

About Can-Fite

Can-Fite BioPharma Ltd. is a public company, traded on the Tel-Aviv Stock Exchange that is headquartered in Petach-Tikva, Israel. The company, which began its operations at the end of 2000 was founded based on the work by Professor Pnina Fishman, formerly a Tumor Immunologist in the Rabin Medical Center The Rabin Medical Center is a medical center in Petah Tikva, Israel. It is currently the second largest medical center in Israel after Sheba Medical Center, having lost the title of largest in 2006.  and currently the company's CEO, together with Dr Ilan Cohn, Patent Attorney and Senior Partner at Reinhold Cohn and Partners, a leading Israeli Patent Attorney firm. The Company has research laboratories and offices in Israel. The Company's lead drug, CF101, for the treatment of rheumatoid arthritis rheumatoid arthritis

Chronic, progressive autoimmune disease causing connective-tissue inflammation, mostly in synovial joints. It can occur at any age, is more common in women, and has an unpredictable course.
 is currently in Phase II clinical trials and to date went through clinical trials in the USA, UK and Israel.

About CF101

CF101 is a small molecule, which is administered to patients orally. This drug, which is developed for the treatment of rheumatoid arthritis, was tested to date in clinical trials in the USA, UK and Israel. The drug is active against a wide variety of autoimmune and cancer diseases and has a preferential safety profile. The drug's main advantage is in its ability to specifically attack pathological cells without affecting healthy ones. In addition, the fact that the drug is administered orally in the form of a capsule creates a huge advantage vs. current treatments which are administered by IV infusion or injection, at much higher costs.

Rheumatoid arthritis (RA) is a severe and chronic autoimmune disease autoimmune disease, any of a number of abnormal conditions caused when the body produces antibodies to its own substances. In rheumatoid arthritis, a group of antibody molecules called collectively RF, or rheumatoid factor, is complexed to the individual's own gamma  that affects more than 1% of the population in the Western World. The disease is characterized mainly by inflammation of the lining, or synovium, of the joints that can lead to long-term joint damage, resulting in chronic pain, loss of function and disability. The market of disease modifying anti-rheumatic drugs Disease Modifying Anti-Rheumatic Drugs (DMARDs)
A class of antirheumatic drugs, including chloroquine, methotrexate, cyclosporine, and gold compounds, that influence the disease process itself and do not only treat its symptoms.

Mentioned in: Antirheumatic Drugs
 is estimated to be about US$ 5 billion and is expected to rise to about $7 billion by 2007.
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Publication:Business Wire
Date:Jan 24, 2006
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