NIAID
Announces Cancellation of "PAVE 100" Preventive HIV Vaccine Trial HIV
preventive vaccine research was dealt another setback last week when the National
Institute of Allergy and Infectious Diseases (NIAID) announced that it would not
proceed with a large planned trial.
As
previously reported, NIAID's HIV Vaccine Trials Network and Merck halted development
of the V520 (MRKAd5) vaccine candidate last fall, after interim data showed that
it did not lower the risk of HIV infection or slow disease progression among 3000
participants in the STEP trial. Further analysis revealed that vaccine
recipients appeared to actually have an increased risk of HIV infection, although
this was limited to male volunteers with pre-existing immunity to the adenovirus
type 5 (Ad5) vector used to carry HIV antigens in the vaccine.
These findings
prompted considerable debate about the future of preventive vaccine research.
At the Conference on Retroviruses and Opportunistic Infections (CROI 2008) this
past February, the
STEP researchers reported that uncircumcised men who received the vaccine
were 4 times more likely to become infected with HIV than uncircumcised placebo
recipients (though there was no significant difference among circumcised men).
Reviewing data from studies to date, Ronald Desrosiers of Harvard Medical School
and Neal Nathanson of the University of Pennsylvania both offered pessimistic
assessments about the current course of vaccine research, with Dr. Nathanson urging
investigators to go "back to the drawing board" of basic science to
devise more promising approaches.
Now, NIAID has announced that it "will
not move forward" with the PAVE 100 trial, which was designed to study a
vaccine candidate using an Ad5 vector like the one in the failed V520 product
in 8500 volunteers in the U.S. and around the world. The PAVE 100 trial was initially
scaled down to include only 2400 circumcised men in the U.S. without pre-existing
adenovirus immunity, but then was cancelled completely. However, NIAID director
Anthony Fauci said the candidate vaccine may still be tested in smaller studies
to see if it lowers viral load among people who do contract HIV, thus working
as a therapeutic rather than a preventive vaccine.
Below is the text
of a NIAID media release announcing the cancellation: NIAID
Will Not Move Forward With the Pave 100 HIV Vaccine Trial VRC
vaccine regimen under consideration for a smaller, more focused study July
17, 2008 -- After soliciting and considering broad input from the scientific and
HIV advocacy communities, the National Institute of Allergy and Infectious Diseases
(NIAID), part of the National Institutes of Health (NIH), has determined that
it will not conduct the HIV vaccine study known as PAVE 100. However, NIAID believes
the vaccine developed by its Vaccine Research Center (VRC) is scientifically intriguing
and sufficiently different from previously tested HIV vaccines to consider testing
it in a smaller, more focused clinical study. Therefore, NIAID will entertain
a proposal for an alternative study with one specific goal: to determine if the
vaccine regimen significantly lowers viral load -- the amount of HIV in the blood
of vaccinated individuals who may later become infected with HIV.
The original
PAVE 100 study, as presented to NIAID's AIDS Research Advisory Committee in January
2007, proposed to test the VRC's HIV vaccine regimen in a trial initially designed
to enroll 8,500 volunteers in the United States, South America, the Caribbean
and Eastern and Southern Africa. The study was to begin U.S. recruitment in October
2007 but was postponed last fall following the decision to halt immunizations
in the STEP HIV vaccine study (see
http://www3.niaid.nih). That decision was made after it was determined that
the vaccine used in the STEP trial, an investigational product developed by Merck
& Co., Inc., failed to prevent HIV infection or reduce viral load.
Subsequent
analyses of the STEP trial found increased numbers of HIV infections among those
volunteers who received the vaccine in comparison to those who received the placebo;
the Merck vaccine itself did not cause HIV infection. The highest risk of HIV
infection among vaccinees compared with placebo recipients appeared to be among
males who were both uncircumcised and had pre-existing neutralizing antibodies
to adenovirus type 5 (Ad5), the common cold virus used in the vaccine as a carrier
for the HIV genes. Vaccination resulted in no apparent increased risk in men who
were circumcised and who lacked pre-existing neutralizing antibodies to Ad5. The
VRC vaccine regimen that was to be tested in the PAVE 100 study has two components,
one of which includes an Ad5-based carrier, which is administered to boost immune
responses that are first stimulated with a DNA vaccine.
Based on the analyses
of the STEP study results, PAVE 100 was redesigned and reduced somewhat in its
proposed scope, although it remained a scientifically and logistically complex
study. The redesigned PAVE 100 study would have involved testing the VRC vaccine
in 2,400 U.S.-based, circumcised men who have sex with men and who lack preexisting
neutralizing antibodies to Ad5. The redesigned study would have tested the vaccine's
effect on viral load, provided additional safety information about the product,
and examined in detail immune responses to the vaccine and their impact on viral
load.
Based on the available scientific information, NIAID has decided
that the VRC vaccine regimen did not warrant a trial of this size and scope and
that PAVE 100 will not proceed. However, NIAID will entertain a smaller, more
focused clinical trial designed to answer one important question: Does the product
have a significant effect on HIV viral load? If such an effect is noted, then
additional studies or expansion of the study to carefully examine immunological
correlates could be performed. NIAID will consider such an alternative study and
will announce its decision at a later time.
An HIV vaccine continues to
be our best hope for ending the HIV pandemic. NIAID is committed to supporting
the basic research and vaccine discovery needed to design promising vaccine candidates
and testing those candidates when appropriate. For information about clinical
HIV vaccine research supported by NIAID, see http://clinicaltrials.gov.
NIAID is a component of the National Institutes of Health (NIH). Press
releases, fact sheets and other NIAID-related materials are available on the NIAID
Web site at www.niaid.nih.gov. For more
information about NIH and its programs, visit www.nih.gov.
|
7/22/08 Sources NIAID.
NIAID Will
Not Move Forward With The Pave 100 HIV Vaccine Trial. Press release.
July 17, 2008. S
Russell. U.S. cancels test of experimental AIDS vaccine. San Francisco Chronicle.
July 18, 2007.
|