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Strategies & Market Trends : Biotechnology Cancer Cures -- Ignore unavailable to you. Want to Upgrade?


To: SnowShredder who wrote (154)5/17/2000 11:13:00 PM
From: david james  Respond to of 226
 
Cancer Conference Could Give Boost to Biotechnology
Companies
By Kristin Reed
quote.bloomberg.com
New Orleans, May 17 (Bloomberg) -- Sagging biotechnology
stocks could get a boost when researchers discuss experimental
cancer drugs from ImClone Systems Inc., Amgen Inc., and Allos
Therapeutics Inc. at a medical meeting opening on Saturday.

Cancer research, long the realm of big pharmaceutical
companies like Bristol-Myers Squibb Co., is becoming dominated by
smaller biotechnology firms testing drugs that doctors hope will
be more effective with fewer side effects.

Biotechnology stocks have slumped in recent weeks after
rocketing earlier this year, in part on the success of cancer
drugs like Herceptin from Genentech Inc., and Rituxan from
Genentech and Idec Pharmaceuticals Corp. Encouraging news at the
meeting of the American Society of Clinical Oncology could help
restore enthusiasm for biotechnology, investors said.
``It's going to take real information to get things going,''
said Stephen Flaks, manager of Flaks Partners LP hedge fund.
``ASCO could be the springboard that takes the group higher.''

The ASCO meeting begins on Saturday, May 20 and will run
through Tuesday, May 23.

The Nasdaq Biotechnology Index gained more than 80 percent in
the first nine weeks of 2000, amid enthusiasm for biotech and
genetic research technology. Since March 6, the index has fallen
37 percent as investors fled technology stocks.

Of the 369 drugs in development that use biotechnology, 175
are designed to treat cancer and with the ASCO meeting, investors
will have a chance to look at data from human studies of some of
the most promising biotech compounds.

New York-based ImClone will offer some of the most eagerly
anticipated data at the conference, presenting research on its
most advanced drug, known as IMC225. The drug works by disabling
one of the defense mechanisms that enables tumors to withstand
chemotherapy or radiation.

Cancer at Molecular Level

IMC225 could be win U.S. Food and Drug Administration
approval as early as next year, according to company officials.
ImClone shares more than quadrupled in the first nine weeks of the
year and are still trading at more than double their January
level.
``The ImClone (data) is a big deal,'' said Jim McCamant, an
analyst with the Medical Technology Stock Letter. ``If they do the
job that they are going to try and do, people will see that it is
some of the most important work in cancer, treating cancer at the
molecular level of the disease.''

Researchers will present data from studies testing the drug
in patients with head and neck cancer and colorectal cancer.

Vical Inc., a San Diego biotechnology company working on gene-
based cancer treatments, will show data on its gene therapy,
Allovectin-7, designed to help the immune system recognize and
attack cancer cells. The drug has been tested against metastatic
melanoma, and in patients with head and neck cancer.

More Effective Radiation

Denver, Colorado based Allos will offer research on its drug,
RSR13, designed to make radiation therapy more effective. The
company is testing the drug for a number of uses, and will present data on whether it may help patients with various types of brain
cancer, including cancer that has metastasized, or spread, to the
brain from other places in the body.
``We are really excited about it,'' said Stephen Hoffman,
president and chief executive officer at Allos. ``The preliminary
data looks very promising and it's a very significant medical
problem.''

Matrix Pharmaceutical Inc. is expected to release the key
data from a study of its IntraDose drug in head and neck cancer
patients. Shares in the Fremont, California based biotech firm
have gained 41 percent over the past two weeks, buoyed by
investors' hopes that the drug will show strong results.

Amgen, the world's largest biotechnology company, could
benefit from data on sustained-release versions of its Epogen and
Neupogen drugs. Epogen is the biggest product for Amgen, the
world's biggest biotechnology company, and brought in slightly
more than half of the company's $3.3 billion in revenue last year.
Neupogen had 1999 sales of $1.26 billion.

Researchers will show data aimed at supporting long-acting
versions of both Epogen and Neupogen.

And Genentech, the oldest biotechnology company, will present
data on an array of experimental cancer drugs, as well as on new
uses for approved drugs such as Herceptin, which with sales of
$188.4 million in 1999, recorded the highest first year sales of
any cancer product in the U.S.

Safety of Genentech Drug

Investors will also be looking closely at the safety of one
of Genentech's experimental drugs, a so-called anti-VEGF drug
designed to shrink tumors by cutting off their blood supply.
Concerns over the drug's safety were sparked last month after six
of 67 lung-cancer patients taking the drug in a study coughed up
blood in incidents that were described as sudden or severe. Four
patients died from complications stemming from those episodes.

Data from that study, released in summary form last month,
will be presented in greater detail at the ASCO conference.

The anti-VEGF drug is one of the most advanced in a class of
experimental cancer therapies known as angiogenesis inhibitors
which work by strangling blood flow to a tumor. If doctors become
worried about safety of anti-VEGF after seeing the more complete
data, that could trigger closer scrutiny of similar drugs in
development at companies such as EntreMed Inc. and Pharmacia Corp.



To: SnowShredder who wrote (154)5/17/2000 11:18:00 PM
From: david james  Read Replies (1) | Respond to of 226
 
Their cash and equity position in Abgenix is still larger than their market cap. One of these days this science is going to be worth something in terms of their market cap.

CEGE will also be presenting their cancer vaccine results (phase II clinical trials) at ASCO

Cell Genesys Reports Encouraging Preclinical Data for GVAX(R) Vaccine in Acute Leukemia

Studies Demonstrated Improvement in Tumor-Free Survival

FOSTER CITY, Calif., May 17 /PRNewswire/ -- Cell Genesys, Inc. (Nasdaq: CEGE - news) collaborators at Johns Hopkins University reported today that in animal studies of
acute leukemia, GVAX© cancer vaccine, administered following bone marrow transplantation, significantly prevented tumor relapse and increased the therapeutic benefit of
transplantation. Tumor-free survival rates were approximately 80 percent in animals receiving the combination of GVAX© vaccine and transplantation, 40 percent in animals
receiving vaccination alone and zero percent in animals receiving neither treatment. Additionally, GVAX© vaccination resulted in the sustained production of an expanded population
of tumor-specific immune cells, thereby redirecting the immune system to recognize and destroy tumor cells. This study, published by Hyam I. Levitsky, M.D., Ivan Borrello, M.D.,
and their colleagues at Johns Hopkins University School of Medicine in the May 15, 2000 issue of the journal, ``Blood,'' provides a model for how to use GVAX© cancer vaccine
following bone marrow transplantation in humans with hematologic cancers such as acute leukemia and multiple myeloma. Human clinical trials for GVAX© vaccine in leukemia
and myeloma are currently planned to start during the next year.

``These preclinical data strongly support the initiation of human clinical trials in GVAX© cancer vaccine following bone marrow transplantation in patients with acute leukemia and
other hematologic malignancies,'' stated Dr. Levitsky, associate professor of oncology and medicine at Johns Hopkins University School of Medicine. ``Although autologous bone
marrow transplantation is currently employed in the treatment of acute leukemia and multiple myeloma, relapse rates remain unacceptably high. We are encouraged that in these
preclinical studies, GVAX© cancer vaccine not only significantly reduced tumor relapse but also resulted in the generation of a sustained increase in the numbers of antitumor
immune cells, increasing the therapeutic benefit of transplantation.''

In the preclinical study described in the ``Blood'' paper, GVAX© cancer vaccine was administered to two groups of mice -- those which received marrow transplants and those which
did not. It was observed that post-transplant administration of GVAX© generated more effective antitumor immune responses than vaccination in the non-transplant group in several
distinct assays of immune function. It was also reported that GVAX© vaccine resulted in the sustained activation of tumor-specific immune cells and that this effect correlated
closely with improved tumor-free survival in the transplant animals.

Autologous (patient-specific) bone marrow transplantation is currently being used to treat hematologic cancers in order to reduce the bone marrow toxicity of high dose
chemotherapy. In the human trials of GVAX© vaccine in acute leukemia and multiple myeloma that are currently being planned, patients will be treated with chemotherapy to induce
remission and will then be vaccinated before and after autologous bone marrow transplantation. The form of GVAX© vaccines used in these trials will be a mixture of the patient's
irradiated tumor cells collected prior to chemotherapy and a non-patient specific GVAX© product produced at Cell Genesys. The goal of GVAX© vaccine therapy in this setting is
to stimulate an immune response directed against the patient's tumor cells and prolong the remission induced by chemotherapy and transplantation.