A Study to Evaluate Safety, Tolerability and Immune Response in Adults Allergic to Peanut After Receiving Intradermal or Intramuscular Administration of ASP0892 (ARA-LAMP-vax), a Single Multivalent Peanut (Ara h1, h2, h3) Lysosomal Associated Membrane Protein DNA Plasmid Vaccine

Exclusion Criteria

• •Subject has severe anaphylaxis to peanuts (Grades 4 or 5 including dyspnea associated with hypoxia, cyanosis, hypotension, or neurological compromise) per the Grading of Food-Induced Anaphylaxis According to Severity of Clinical Symptoms based on historical clinical symptoms.
• •Subject develops a Grade 4 or 5 reaction during the DBPCFC.
• •Subject who has received or is planning to receive administration of any vaccine (other than injectable Influenza vaccine) within 28 days prior to the administration of the study vaccine or at any time during the study.
• •Subject who received any specific immunotherapy for allergy (e.g., epicutaneous immunotherapy \[EPIT\], sublingual immunotherapy \[SLIT\], subcutaneous immunotherapy \[SCIT\], and oral immunotherapy \[OIT\]) during the past 12 months, currently, or plans to receive during the course of the study.
• •Subject who has used the following drug(s) prior to the dosing of the study vaccine:
• •* Within 2 months prior to study vaccine administration: Systemic (or inhaled) steroid, chemical mediator-isolation inhibitor, Th2 cytokine inhibitor, thromboxane A2 synthesis inhibitor, thromboxane A2 receptor antagonist, β-blocker, angiotensin-converting enzyme inhibitors, and/or angiotensin-receptor blockers
• •* Within 3 months prior to study vaccine administration: Biologics and/or immune modulators (including anti-TNFα antibody and anti-IgE monoclonal antibody)
• •Subject who has history of allergic reactions such as anaphylactic shock, angioedema with airway constriction or hypotension caused by food other than peanut and/or medical products (including vaccine) in the past.
• •Subject's laboratory test results at screening or prior to study vaccine dosing on day 1 are outside the normal limits and considered to be clinically significant.
• •Subject with anti-LAMP-1 antibodies above the cut-point for the Tier 1 assay and who is confirmed positive in the Tier 2 assay at Screen 1 visit (baseline).
• •Subject who had a positive test results for hepatitis B surface (HBs) antigen, hepatitis C virus (HCV) antibody, or human immunodeficiency virus (HIV) antigen/ antibody.
• •Subject who has immune disorders (including autoimmune disease) and/or diseases requiring immunosuppressive drugs.
• •Subject who was diagnosed with immunodeficiency in the past.
• •Subject who has uncontrolled hypertension.
• •Subject who has a history of cardiovascular disease, arrhythmias, chronic lung disease, active eosinophilic gastrointestinal disease, or any other medical or surgical conditions which places the subject at increased risk for participation in the study.
• •Subject who has a complication or medical history of respiratory disease which requires medical treatment.
• •Subject who has a complication or medical history of malignant tumor.
• •Subject who has mental conditions such as schizophrenia, bipolar disorder, and major depressive disorder, or a subject who has received drug(s) for the treatment of dementia.
• •Subject who has severe or poorly controlled dermatitis atopic or generalized eczema.
• •Subject who is unable to discontinue antihistamines within 7 days or 5 half-lives (whichever duration is longer) as follows:
• •* prior to dosing through 7 days post last dose of study vaccine
• •* prior to skin prick testing and oral food challenge procedures
• •Subject who has asthma other than mild intermittent asthma (National Heart, Lung, and Blood Institute \[NHLBI\] guidelines) and has a FEV1 value \< 80% and/or requiring chronic maintenance treatment (i.e., inhaled corticosteroids).
• •Subject who has already received vaccination of LAMP-vax such as ASP0892.
• •Subject who has received investigational therapy within 35 days or 5 half- lives whichever is longer, prior to screening.
• •Subject who is an employee of the Astellas Group or vendors involved in the study.
• •Subject who has any condition which makes the subject unsuitable for study participation.