| City: |
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St. Louis |
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State:
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MO |
| Zip Code: |
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63104 |
| Conditions: |
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Influenza |
| Purpose: |
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The purpose of this study is to see how the body reacts to different strengths of the H1N1
flu shot in persons infected with human immunodeficiency virus (HIV). This study will also
compare how the CD4 count (cells that help fight disease) affects the body's response to the
H1N1 flu shot. In this study, 2 strengths of the H1N1 flu shot will be given twice, about 3
weeks apart. The results of this study will help researchers find out if the different
strengths of the H1N1 flu shot make the body produce H1N1 antibodies that are better at
fighting H1N1 flu. About 240 HIV positive subjects, ages 18-64 years, will be asked to take
part in this study. Study procedures include: blood sampling, physical exams, and use of
memory aids to record temperature, medications and symptoms. The length of patient
participation is about 7 months.
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| Study summary: |
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Recently, a novel swine-origin influenza A/H1N1 virus was identified as a significant cause
of febrile respiratory illnesses in Mexico and the United States. It rapidly spread to many
countries around the world, prompting the World Health Organization (WHO) to declare a
pandemic on June 11, 2009. The immunosuppression associated with human immunodeficiency
virus (HIV)-infection has been related to diminished immune responses to vaccination against
multiple pathogens, including influenza. The widespread use of antiretroviral therapy has
resulted in a significant decrease in the mortality from HIV/acquired immune deficiency
syndrome (AIDS) and, as a result, HIV-infected subjects constitute a demographically growing
subpopulation in the United States. Currently, novel H1N1 vaccines are being evaluated in
the general population. Researchers propose to evaluate the safety and immunogenicity of the
novel H1N1 vaccines in HIV-infected subjects, because the data from clinical trials
enrolling healthy subjects may not apply to immunosuppressed individuals; and an evaluation
of the immune responses to vaccination against new, pandemic influenza viruses has never
been performed in HIV-infected subjects. This is a randomized, open label, Phase II study in
HIV seropositive males and non-pregnant females, aged 18-64 years. This study is designed to
investigate the safety, reactogenicity, and immunogenicity of an inactivated influenza H1N1
virus vaccine at 2 dose levels. Subjects will be randomized into 2 dose groups, stratified
by cluster of differentiation (CD4) cell count at enrollment (120 subjects per dose group
with 60 subjects per CD4 cell count stratum, <200/mL or greater than or equal to 200/mL) to
receive intramuscular (IM) inactivated influenza H1N1 vaccine at 15 mcg (Group 1) or 30 mcg
(Group 2). The H1N1 vaccine will be administered at Day 0 and Day 21. Following
immunization, safety will be measured by assessment of adverse events through 21 days
following the last vaccination (Day 42 for those receiving both doses and Day 21 for those
who do not receive the second dose), serious adverse events and new-onset chronic medical
conditions through 7 months post first vaccination (Day 201), and reactogenicity to the
vaccine for 8 days following each vaccination (Day 0-7). A CD4/CD8 panel and viral load will
be measured prior to first vaccination on Day 0 and at Day 10 post the second vaccination.
Immunogenicity testing will include hemagglutination inhibition assay (HAI) and neutralizing
antibody testing on serum obtained on the day of each vaccination (prior to vaccination), on
Day 10 after each vaccination, 21 days following the second vaccination (Day 42) and 6
months after the second vaccination (Day 201). The primary objectives of this study are:
(safety), to assess the safety of the unadjuvanted, inactivated H1N1 vaccine in HIV-1
seropositive adults when administered at the 15 mcg or 30 mcg dose and (immunogenicity) to
assess the antibody response following 1 and 2 doses of inactivated H1N1 vaccine
administered intramuscularly at the 15 mcg or 30 mcg dose levels in HIV-1 seropositive
adults stratified by CD4 count at enrollment. |
| Criteria: |
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Inclusion Criteria:
- Human immunodeficiency virus (HIV) infection defined as documented by an
enzyme-linked immunosorbent assay (ELISA) and confirmed with a Western blot at any
time prior to study entry. Serum HIV-1 antigen, plasma HIV-1 ribonucleic acid (RNA),
or any Food and Drug Administration (FDA) approved antibody test by a method other
than ELISA is acceptable as an alternative confirmatory test.
- Males or non-pregnant females age 18-64, inclusive.
- Women of child-bearing potential (not surgically sterile via tubal ligation,
bilateral oophorectomy or hysterectomy or who are not postmenopausal for greater than
or equal to 1 year) must agree to practice adequate contraception that may include,
but is not limited to, abstinence, monogamous relationship with vasectomized partner,
barrier methods such as condoms, diaphragms, spermicides, intrauterine devices,
Depo-Provera injections or Implanon implants for at least 30 days following the last
vaccination.
- Are medically stable, as determined by the Investigator (based on review of health
status, vital signs, medical history, and targeted physical examination. Vital signs
must be within normal ranges prior to the first vaccination (heart rate 55-100, blood
pressure systolic <160, blood pressure diastolic <90).
- Receipt of the 2009-2010 seasonal influenza vaccine at least two weeks prior to
enrollment in this study.
- Intend to be available for follow-up visits and phone call access through 7 months
following receipt of H1N1 vaccine.
- Are able to understand and comply with planned study procedures.
- Subject receiving regular medical follow-up care for HIV.
- Has a documented platelet count of >50,000mm^3 and an absolute neutrophil count (ANC)
of >500mm^3 within the 3 months prior to study entry.
- Provide written informed consent prior to initiation of any study procedures.
Exclusion Criteria:
- Treatment for an opportunistic infection (OI) initiated within 2 weeks prior to
enrollment, or have symptoms that have not stabilized.
- Have a known allergy to eggs or other components of the vaccine (including polymyxin,
neomycin, and chicken protein).
- Women who are pregnant or breastfeeding.
- Have a positive urine or serum pregnancy test within 24 hours prior to vaccination.
- Use of anticancer chemotherapy or radiation therapy (cytotoxic) within the preceding
36 months.
- Have a neoplastic disease that will be treated with chemotherapy or radiation, or a
history of any hematologic malignancy.
- Have long term use of glucocorticoids including oral, parenteral or high-dose inhaled
steroids. For oral or parenteral: prednisone or equivalent (greater than or equal to
2.0 mg/kg per day or greater than or equal to 20 mg total dose) for more than 2
consecutive weeks (or 2 weeks total) in the past 3 months. For inhaled steroids:
>800 mcg/day of beclomethasone dipropionate or equivalent within the preceding 6
months. (Nasal and topical steroids are allowed.)
- Have an uncontrolled major psychiatric diagnosis.
- Have a history of receiving immunoglobulin or other blood products within the 3
months prior to vaccination in this study.
- Received an experimental agent (vaccine, drug, biologic, device, or medication)
within 1 month prior to vaccination in this study or expect to receive an
experimental agent during this study (prior to the Day 201 follow-up call).
- Have received any live licensed vaccines within 4 weeks or inactivated licensed
vaccines within 2 weeks prior to vaccination in this study or plan receipt of such
vaccines within 21 days following the second vaccination.
- Have an acute or chronic medical condition that, in the opinion of the investigator,
would render vaccination unsafe, or would interfere with the evaluation of responses.
- Have a history of severe reactions following previous immunization with influenza
virus vaccines.
- Have a moderate-severe acute illness, including an oral temperature greater than
100.4 degrees Fahrenheit, within 72 hours prior to vaccination. (This may result in a
temporary delay of vaccination).
- Have any condition that would, in the opinion of the site investigator, place them at
an unacceptable risk of injury or render the subject unable to meet the requirements
of the protocol.
- Participated in a novel influenza 2009 H1N1 influenza vaccine study or have history
of novel 2009 H1N1 influenza infection prior to enrollment.
- Have a history of alcohol or drug abuse in the last 3 months.
- Plan to travel outside of North America at any time between the first vaccination and
42 days following the first vaccination.
- Have a history of Guillain-Barré Syndrome.
- Have any condition that the investigator believes may interfere with successful
completion of the study. |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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April 13, 2010 |
Modifications to
this listing: |
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Only selected fields are shown, please use the link
above to view all information about this clinical trial. |
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