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WEEK IN REVIEW
Sunday


Fighting foreclosure: How one couple got caught...
Monroe man's family remembers a life devoted to...
155-year boys club comes to an end
Saturday
How to avoid holiday thieves
Burn ban orders will have new teeth
Get a flu shot now, officials urge
Friday


A community in limbo
Ideas arise on housing sex offenders
Turnout for historic election breaks county and...
Thursday


Ways to Give: Where you can make a difference
Ways to give: Charities hit hard from both sides
County Council cuts deeply from most staff exce...
Wednesday


Cancer survivor is again living the life of a t...
Tulalip school is grieving once more
Faulty part bogs down Boeing's jet lines
Tuesday


'We are devastated' by loss of two boys, family...
A scramble to shave $1.8 million from county bu...
Arlington about to add land; buildup could follow
Monday


Arlington boys couldn't be saved from fire
Mom heeds call to serve
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CONTACT THE HERALD
Mike Benbow, Business Editor
benbow@heraldnet.com
 
Published: Friday, March 21, 2008

Bothell's Seattle Genetics pitches drug combo

Clinical trial starts for pair to fight 'preleukemia'

BOTHELL -- Seattle Genetics is studying whether combining one of its engineered antibodies with a cancer drug could help patients with a condition that attacks the body's bone marrow.

The Bothell-based biotechnology firm said Thursday it has begun a phase 1 clinical trial to test the safety and effectiveness of SGN-33 when it is taken with the cancer drug Revlimid to treat myelodysplastic syndromes, which disrupt bone marrow's production of blood cells.

The trial is being conducted in concert with Celgene Corp., the maker of Revlimid.

SGN-33 works by targeting the CD33 antigen, which is expressed in a number of blood-related cancers.

The drug candidate already is in phase 2 tests as a treatment for acute myeloid leukemia and has received "orphan drug" status from the Food and Drug Administration for that use. That status, designed to encourage new drugs for relatively rare diseases, offers potential government funding and tax credits, as well as protection from competition.

It makes sense to test the drug against myelodysplastic syndromes, because it is related to the leukemia already being targeted by Seattle Genetics, said Thomas Reynolds, the biotech's chief medical officer.

"Patients with intermediate and high-risk MDS typically have a poor prognosis and their disease often transforms into acute myeloid leukemia, underscoring the need for a well-tolerated treatment option that can extend overall survival," Reynolds said in Thursday's announcement.

According to the American Cancer Society, an estimated 10,000 to 15,000 new cases of MDS are diagnosed annually in the United States. The syndromes disrupt bone marrow function, usually decreasing the number of red and white blood cells and or platelets.

About 30 percent of patients with the syndromes eventually develop leukemia. Because of that, MDS also is sometimes called "smoldering leukemia" or "preleukemia."

SGN-33 is one of three drugs Seattle Genetics has in human-testing trials. The company's most advanced drug candidate is SGN-40, which is being developed with Genentech to treat non-Hodgkin lymphoma and multiple myeloma.

Seattle Genetics' shares rose 26 cents, or 3 percent, Thursday to close at $8.96.



Reporter Eric Fetters: 425-339-3453 or fetters@heraldnet.com.

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