The study seeks to define, with precision, the safety and efficacy of APSV, two dose potencies of one lot in vaccinia-naive adults. The ability of this vaccine to induce a classic �take� as defined by formation of a lesion at the injection site consistent with the �Jennerian� process (see Appendix A) and vaccine specific immune responses will be assessed. The local cutaneous lesion is considered to be a surrogate for clinical effectiveness of live, replicating smallpox vaccines. Neutralizing antibody formation has been correlated with takes for the Dryvax vaccine and is considered to be cross-protective for other orthopoxviruses, including variola. The study also seeks to characterize preliminarily the cell mediated immune (CMI) response to APSV (as compared to Dryvax).

Condition	Treatment or Intervention	Phase
Smallpox	Vaccine: Aventis Pasteur Smallpox Vaccine	Phase II

A Multicenter, double blind, randomized trial in which each volunteer will receive one of 2 dose concentrations of one of two lots of Aventis Pasteur Smallpox Vaccine as a single vaccination (undiluted, 1:5 dilution). Volunteers without a take at day 7 - 9 will be offered a vaccination with Dryvax at the end of the study.

Ages Eligible for Study:  18 Years   -   32 Years,  Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

INCLUSION CRITERIA:

• Adequate renal function defined as a serum creatinine 1.5 mg/dL; urine protein < 100mg/ dL or trace or negative proteinuria (by dipstick), and a calculated creatinine clearance >55 mL/min. Formula for calculations is contained within the Manual of Procedures. (Note: Renal function is measured to ensure that subjects could meet criteria for use of cidofovir if needed).
• Age 18-32 (children are excluded due to concerns of safety, including autoinoculation).
• Willing to sign informed consent.
• Availability for follow-up for planned duration of the study (56 days following the last vaccination).
• Acceptable medical history by screen evaluation form and brief assessment.
• Absence of a typical vaccinia scar and negative history of smallpox vaccination.
• Negative urine or serum pregnancy test for women of childbearing potential.
• If the volunteer is female and of childbearing potential, she agrees to use acceptable contraception, and not become pregnant for the duration of the study. (Acceptable contraception includes implants, injectables, combined oral contraceptives, effective intrauterine devices (IUDs), sexual abstinence, or a vasectomized partner).
• Negative ELISA for HIV or negative Western blot for subjects who have a positive ELISA and have participated in an HIV vaccine trial.
• Negative hepatitis B surface antigen and negative antibody to hepatitis C virus.
• Negative urine glucose by dipstick.
• ALT < 1.5 times institutional upper limit of normal.

EXCLUSION CRITERIA:

• Allergies to any component of the vaccines (e.g., polymyxin B sulfate, dihydrostreptomycin sulfate, chlorotetracycline hydrochloride).
• History of immunodeficiency.
• Serology positive for HIV, hepatitis B, or hepatitis C at the screening visit.
• Known or suspected impairment of immunologic function including, but not limited to clinically significant liver disease.
• Diabetes mellitus.
• Moderate to severe kidney impairment.
• Malignancy with the exception of squamous cell or basal cell skin cancer.
• Autoimmune disease.
• Use of immunosuppressive medication.
• Corticosteroid nasal sprays are permissible.
• Medical or psychiatric condition or occupational responsibilities which preclude subject compliance with the protocol.
• History of illegal injection drug use.
• Live attenuated vaccines within 60 days of study.
• Use of experimental agents within 30 days prior to study.
• Any history of vaccination with any vaccinia vectored or other pox vectored experimental vaccine.
• Smallpox vaccination since 1990 (Vaccinia experience cohorts).
• Typical vaccinia scar or history of smallpox vaccination (Vaccinia naive cohorts only).
• Receipt of blood products or immunoglobulin in the past 6 months.
• Recent donation of the equivalent of a pint of blood within the 30 days prior to enrollment.
• Acute febrile illness (100.5 F) on the day of vaccination.
• Pregnant or lactating women.
• Eczema of any degree or history of eczema.
• History of exfoliative skin disorders/conditions.
• Any acute skin disorders of large magnitude, e.g., laceration requiring sutures, burn greater than 2x2 cm.
• Household contacts/sexual contacts with, or close and frequent occupational exposure to, any of the following: pregnant women, children < 12 months of age, people with eczema or history of eczema, people with any of the skin disorders/conditions previously listed, people with immunodeficiency disease or use of immunosuppressive medications.
• Any condition which, in the opinion of the investigator, might interfere with study objectives.

Iowa
      University of Iowa - Iowa City IA, Iowa City,  Iowa,  52242,  United States
Ohio
      University of Cincinnati, Cincinnati,  Ohio,  45267-05,  United States
      Cincinnati Children's Hospital Med Ctr, Cincinnati,  Ohio,  45229,  United States
Tennessee
      Vanderbilt University, Nashville,  Tennessee,  37232-26,  United States

Study ID Numbers:  02-054
Record last reviewed:  July 2004
Record first received:  December 11, 2002
ClinicalTrials.gov Identifier:  NCT00050518
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2004-10-14