Researchers moving toward new anthrax vaccine with fewer shots
October 4, 2002
By LAURA MECKLER
Associated Press Writer
(AP) WASHINGTON
Two private companies were starting work to create a new, genetically
engineered anthrax vaccine that promises to cut in half the six shots needed
for protection, building on technology developed by federal researchers.
The Department of Health and Human Services awarded contracts worth $22.5
million to California-based VaxGen Inc. and Britain's Avecia to test the
experimental vaccine on people to see if it is safe and, if so, to see if it
provides protection against the deadly bacteria.
Federal authorities hope that together, the two companies will pave the way
toward Food and Drug Administration approval for the vaccine. Eventually,
the government wants 25 million doses manufactured and added to the National
Pharmaceutical Stockpile.
VaxGen said it plans to begin testing for safety by mid-2003 and finish by
the end of next year.
The current anthrax vaccine works well, experts say, but it requires six
shots over 18 months plus an annual booster and it causes side effects. Last
spring, a scientific advisory panel endorsed the existing shots, but
recommended development of the next generation of vaccine, one that would
require fewer shots and cause fewer side effects.
The search for a replacement took on new urgency after last fall's anthrax
attacks, discovered a year ago Friday when health officials announced that a
Florida man had mysteriously contracted the disease. Later, as more cases
emerged, investigators learned that the spores were being spread through the
mail.
"There is an urgent need to devise more effective measures to protect U.S.
citizens from the harmful effects of anthrax spores used as instruments of
terror," HHS Secretary Tommy Thompson said in a statement Thursday
announcing his agency's grants.
Federal scientists working at the Army's lab at Fort Detrick, Maryland, have
already developed the science behind the promising new vaccine. There are
three proteins that make anthrax deadly, and all must work in concert to
cause infection. The experimental vaccine engineers one of them, called
protective antigen, which stimulates the body's immune system so that it can
recognize and fight anthrax should the person actually be infected later.
The private companies must now try to translate this technology into a
practical vaccine. They must create samples for testing, then test the
vaccine on a few people to see if it is safe. If these so-called Phase I
trials work, the vaccine would be tested on larger groups of people to
ensure it protects against infection _ steps vital for the FDA to ultimately
approve its sale.
On Thursday's news, VaxGen stock rose 13 percent, or $1.17 per share, to
close at $10.17 in trading on the Nasdaq Stock Market. Avecia is privately
held.
The existing vaccine, manufactured by BioPort of Lansing, Michigan, also
uses the protective antigen, but the protein was not genetically modified
using today's modern techniques, said Robert Myers, BioPort's executive vice
president. He added that his company's vaccine may also be effective when
delivered in two or three doses, testing that is now under way.
The current vaccine is not now offered to civilians who have not been
exposed to anthrax. It is, however, routinely used by the Pentagon.
All existing vaccine was under control of the Defense Department until this
summer, when HHS and the Pentagon agreed to split the stockpile and each
take half.
Copyright 2001 Associated Press. All rights reserved.
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