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Keep this study
Lead
MedImmune LLC
Age
18–40
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Male or female ages 18 through 40 years (not yet reached their 41st birthday) on the day of randomization
Healthy by medical history and physical examination
Available by telephone
Signed written informed consent and Health Insurance Portability and Accountability Act (HIPAA) authorization obtained from the volunteer
Sexually active females, unless surgically sterile or at least 1 year post-menopausal, must have used an effective method of avoiding pregnancy (including oral, implanted, or transdermal contraceptives, intrauterine device (IUD), female condom, diaphragm with spermicide, cervical cap, abstinence, use of a condom by the sexual partner or sterile sexual partner) for at least 30 days prior to dosing of study vaccine, and must agree to continue using such precautions for at least 30 days after dosing; the volunteer must also have a negative serum pregnancy test within 7 days prior to dosing of study vaccine and a negative urine pregnancy test on the day of study vaccine dosing prior to administration
Sexually active males, unless surgically sterile, must use an effective method of birth control (condom or abstinence) and must agree to continue using such precautions for at least 30 days after dosing
Ability to understand and comply with the requirements of the protocol as judged by the investigator
Ability to complete the follow-up period of 6 months following dosing as required by the protocol
You may not be if
Acute illness on the day of randomization
Fever (greater than or equal to 99.5°F oral or greater than or equal to 100.1°F tympanic) and/or respiratory illness (e.g., cough or sore throat) within 7 days prior to randomization
Any drug therapy (chronic or other) within 7 days prior to randomization (except for certain medications such as contraceptives, topical \[i.e., dermatologic\] corticosteroids, or infrequent use of over-the-counter pain relievers, following approval from the sponsor) or expected receipt through 28 days after study vaccine dosing
Receipt of immunoglobulin or blood products within 90 days prior to screening or expected receipt through 28 days after study vaccine dosing
Receipt of any investigational drug within 60 days prior to randomization or expected receipt during the study period (i.e., through 180 days after study vaccine dosing)
Receipt of an approved vaccine within 30 days prior to randomization or expected receipt through 28 days after study vaccine dosing
History of immunodeficiency or receipt of immunosuppressive agents, or expected receipt of an immunosuppressive agent through 28 days after study vaccine dosing
Close contact at home or in the workplace with children under 2 years of age
Household contact who is immunocompromised; volunteer should also avoid close contact with immunocompromised individuals for at least 21 days after vaccination
History of hypersensitivity to kanamycin or other aminoglycoside antibiotics (gentamicin, tobramycin, etc.)
Previous medical history, or evidence, of an intercurrent or chronic illness that, in the opinion of the investigator, may compromise the safety of the volunteer
Any evidence of end organ dysfunction
Current, or history of, clinically significant abnormality on electrocardiogram (ECG) (screening ECG must be within 30 days prior to randomization)
Evidence of active infection with HIV or hepatitis A, B, or C virus, or serologic evidence of past infection with hepatitis B or C virus
At screening (must be within 7 days prior to randomization), any of the following laboratory tests outside of the laboratory normal range: CBC: hemoglobin (Hgb), WBC count, platelet count; AST, ALT, BUN, creatinine; or other abnormal laboratory value in the screening panel that, in the opinion of the principal investigator, may potentially confound analysis of study results
Nursing mother
History of alcohol or drug abuse in the past 2 years
History of medical diagnosis of asthma, reactive airway disease, or chronic obstructive pulmonary disease (COPD)
History of any smoking in the past 5 years
Previous vaccination against Respiratory Syncytial Virus (RSV) or Parainfluenza Virus Type 3 (PIV3) in a clinical trial
Employees of the research center, any individuals involved with the conduct of the study, or family members of such individuals
Any condition that, in the opinion of the investigator, might interfere with study vaccine evaluation
Clareo Health | Study to Evaluate MEDI-534 in Healthy Adults
