A Phase II Study on Immunogenicity and Safety of MVA-BN® (IMVAMUNE™) Smallpox Vaccine in Subjects With Atopic Dermatitis



Status:Completed
Conditions:Psoriasis, Infectious Disease, Dermatology, Dermatology, Dermatology
Therapuetic Areas:Dermatology / Plastic Surgery, Immunology / Infectious Diseases
Healthy:No
Age Range:18 - 40
Updated:1/11/2019
Start Date:July 2006
End Date:April 2010

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A Multicenter, Open-label, Controlled Phase II Study to Evaluate Immunogenicity and Safety of MVA-BN® (IMVAMUNE™) Smallpox Vaccine in 18-40 Year Old Subjects With Diagnosed Atopic Dermatitis

The purpose of this study is to compare the immunogenicity and safety of an investigational
smallpox vaccine in subjects with atopic dermatitis to healthy volunteers.


Inclusion Criteria:

Group 1 (Healthy Participants):

Subjects without present or history of any kind of atopy.

Group 2 (Atopic Dermatitis Participants):

Subjects with diagnosed atopic dermatitis.

All study subjects:

1. Male and female subjects between 18 and 40 years of age without history of smallpox
vaccination.

2. Women must have a negative serum pregnancy test at screening and a negative urine or
serum pregnancy test within 24 hours prior to vaccination.

3. Women of childbearing potential must have used an acceptable method of contraception
for 30 days prior to the first vaccination, must agree to use an acceptable method of
contraception during the study, and must not become pregnant for at least 28 days
after the last vaccination.

4. Lab values without clinically significant findings.

5. Electrocardiogram (ECG) without clinically significant findings.

Exclusion Criteria:

1. Pregnant or breast-feeding women.

2. Uncontrolled serious infection i.e. not responding to antimicrobial therapy.

3. History of or active autoimmune disease. Persons with vitiligo or thyroid disease
taking thyroid replacement are not excluded.

4. Known or suspected impairment of immunologic function including, but not limited to,
clinically significant liver disease; diabetes mellitus; moderate to severe kidney
impairment.

5. History of malignancy, other than squamous cell or basal cell skin cancer, unless
there has been surgical excision that is considered to have achieved cure. Subjects
with history of skin cancer at the vaccination site are excluded.

6. History of coronary heart disease, myocardial infarction, angina, congestive heart
failure, cardiomyopathy, stroke or transient ischemic attack, uncontrolled high blood
pressure.

7. History of an immediate family member (father, mother, brother, or sister) who has had
onset of ischemic heart disease before age 50 years.

8. Ten percent or greater risk of developing a myocardial infarction or coronary death
within the next 10 years using the National Cholesterol Education Program's risk
assessment tool: (http://hin.nhlbi.nih.gov/atpiii/calculator.asp?usertype=prof) NOTE:
This criterion applies only to volunteers 20 years of age and older.

9. History of anaphylaxis or severe allergic reaction.

10. Post organ transplant subjects whether or not receiving chronic immunosuppressive
therapy.

11. Administration of immunomodulatory substances.
We found this trial at
16
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Tucson, Arizona 85745
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740 South Limestone Street
Lexington, Kentucky 40536
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Lexington, KY
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Albuquerque, New Mexico 87106
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Albuquerque, NM
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303 East Superior Street
Chicago, Illinois 60611
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Chicago, IL
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Dallas, TX
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Garden Grove, California 92843
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Garden Grove, CA
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Hot Springs, Arkansas 71913
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Hot Springs, AR
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Magdalena De Las Salinas, CP 07760
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Magdalena De Las Salinas,
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Omaha, Nebraska 68134
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Omaha, NE
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Overland Park, Kansas 66211
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Portland, Oregon 97210
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Portland, OR
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Rochester, New York 14623
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Rochester, NY
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Saint Louis, Missouri 63110
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Saint Louis, MO
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Saint Louis, Missouri 63141
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Saint Louis, MO
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San Antonio, Texas 78229
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San Antonio, TX
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Vallejo, California 94589
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Vallejo, CA
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