HHS Announces Contracts to Develop Safer Smallpox Vaccines
HHS Secretary Tommy G. Thompson today announced the award of two contracts
totaling up to $20 million in first-year funding to develop safer smallpox
vaccines. The three-year contracts were awarded to Bavarian Nordic A/S of
Copenhagen, Denmark, and Acambis Inc. of Cambridge, Mass. The National Institute
of Allergy and Infectious Diseases (NIAID) will administer the contracts.
"To protect ourselves from the remote but extremely grave threat of a
deliberate release of smallpox virus, we need a vaccine that can be safely given
to all Americans, including individuals with weakened immune systems, children
and pregnant women," said Secretary Thompson. "The new contracts will help us
meet this need by accelerating research on second-generation smallpox vaccines."
"Milestone-driven contracts such as these are one way NIAID is eliciting
industry participation in the search for new and improved vaccines," noted NIAID
Director Anthony S. Fauci, M.D. "These programs are designed to get reliable
products into the pipeline in an economically efficient and scientifically sound
manner," he added.
Acambis and Bavarian Nordic will develop, manufacture and conduct safety
trials of modified vaccinia virus Ankara (MVA) vaccine candidates. Vaccinia
virus, a close relative of smallpox virus, is used in traditional smallpox
vaccines. A live, replicating virus, vaccinia can cause side effects, which on
rare occasions can be serious and potentially life-threatening. Pregnant women
and people with compromised immune systems, such as patients on chemotherapy or
people with HIV/AIDS, cannot receive the current smallpox vaccine at all.
MVA is a strain of vaccinia that cannot replicate inside human cells and
therefore cannot cause dispersed infection. An MVA-based vaccine given to more
than 120,000 people during the smallpox eradication campaign in Germany in the
1970s had an excellent safety record. When smallpox was declared eradicated in
1980, however, the need for smallpox vaccines vanished, and research on MVA for
that purpose ended.
Because of the urgent need for safer smallpox vaccines, the new contracts
emphasize timely completion of predetermined objectives. For example, within the
first six months the companies must produce several thousand doses of their
prototype vaccine along with data indicating its effectiveness in animal models.
Following approval of human study protocols, the companies will conduct tests of
the vaccines' safety in healthy adults. Finally, the companies must develop a
plan for large-scale manufacture of the candidate vaccines and show how they
could deliver up to 30 million doses to the federal government.
NIAID is a component of the National Institutes of Health (NIH), which is an
agency of the Department of Health and Human Services. NIAID supports basic and
applied research to prevent, diagnose, and treat infectious and immune-mediated
illnesses, including HIV/AIDS and other sexually transmitted diseases, illness
from potential agents of bioterrorism, tuberculosis, malaria, autoimmune
disorders, asthma and allergies.