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To: Jenna who wrote (24976)2/11/1999 3:52:00 PM
From: Dave Gore  Read Replies (1) | Respond to of 120523
 
**ENMD** I apologize if you have seen this amazing cancer news; CBS MARKET WATCH

Anti-cancer results duplicated
Government test big boost for EntreMed

Last Update: 2:18 PM ET Feb 11, 1999
NewsWatch

BOSTON (AP) -- Government scientists have finally been able to
reproduce a scientist's highly publicized results for an anti-cancer drug and
are now seeking to begin the first human tests, The Boston Globe
reported Thursday.

The tiny biotech company EntreMed (ENMD) saw its shares soar on the
news.

The breakthrough using the drug endostatin came only when National
Cancer Institute scientists conducted the experiment in the Children's
Hospital laboratory of researcher Dr. Judah Folkman, who discovered it
and found that it reduced tumors in mice.

Last fall, NCI scientists said they could not match
Folkman's promising test results using a small
quantity of the drug Folkman sent them. Folkman
attributed the failure to the drug's sensitivity to
handling, storage and the way it's administered. The
institute, in Frederick, Md., then sent researchers to
Folkman's lab in November and December.

"This substantiates the idea that these are technical
issues" that led to the failure at the NCI laboratory,
Dr. Robert Wittes, deputy director of the institute,
told the Globe. "Now we will move to facilities in
Frederick and try to reproduce the results down
here," he said.

The NCI also sent notices this week to medical
centers around the country, inviting proposals for
human tests to determine if endostatin is safe, the
newspaper said.

Wittes could not predict when tests on humans
would start.

Folkman gained worldwide attention last spring when The New York
Times reported in a page one story on his findings that endostatin and a
related drug, angiostatin, shrunk tumors in rats by cutting off their blood
supply.

Children's Hospital licensed both drugs to EntreMed for further
development into commercial products. EntreMed sublicensed angiostatin
to the Bristol-Myers Squibb pharmaceutical company, while EntreMed
and the cancer institute concentrated on endostatin.

On Tuesday, Bristol-Myers said it was withdrawing from the partnership
to develop angiostatin, saying the project had not produced a drug that
was consistently effective.

EntreMed said it would press ahead with tests on angiostatin, but
investors sliced the company's value in half Wednesday. Today, shares of
EntreMed rebounded $2.62 1/2, or by 20.4 percent, to $15.50 in
morning trading on the Nasdaq Stock Market.