The Peanut Oral Immunotherapy Study: Safety, Efficacy and Discovery

All arms will undergo an Initial Dose Escalation (IDE) Day and updosing regimen with a
maintenance phase of OIT or placebo to a maximum of 4,000 mg protein daily, as peanut flour,
in the OIT groups, and to a maximum of an equivalent amount of oat flour for the placebo
group. After maintenance is achieved, all subjects will begin performing DBPCFCs (staged so
as to ensure safety) at Week 104 and every 13 weeks thereafter. At Week 104, individuals that
reach criteria will, based on the randomization that was done at the start of the study,
either stop therapy with peanut and be switched to oat flour, or will be maintained on 300 mg
peanut protein per day and all placebo subjects will decrease to the equivalent volume of oat
flour (approximately 600 mg oat flour) to optimize the blind. All subjects will be evaluated
every 13 weeks thereafter with DBPCFCs until the end of study.

Individuals in Arm A will be defined as "clinically tolerant" if there is no clinical
reactivity at the Week 104 and Week 117 DBPCFC. Clinical reactivity is defined as any
reaction ≥ Grade 1 based on the Bock's Criteria. Individuals in Arm A who meet the definition
of "clinically tolerant" will continue to avoid peanut protein (i.e. continue on 600 mg per
day of oat flour) as long as each subsequent DBPCFC (performed every 13 weeks until end of
study) shows no clinical reactivity.

Individuals in Arm B will be defined as "desensitized" to a minimum of 300 mg per day of
peanut protein if they show no clinical reactivity at DBPCFCs (week 117 to end of study).

Individuals in Arm C will be defined as "natural loss of responsiveness" if they show no
clinical reactivity at DBPCFCs (week 117 to end of study).

We plan to identify the basic immune mechanisms which can explain the differences in the
effects of OIT in individuals who do or do not become clinically tolerant and to determine
whether immune monitoring can predict the safety and efficacy outcomes in peanut OIT
protocols.

After initial screening and enrollment, there are three phases of the study:

- Dose escalation and Build up Phase

- Maintenance phase

- Tolerance and Desensitization Testing phase Overall, 120 subjects who are eligible will
undergo the Initial Dose Escalation Day. Subsequent updosing visits will occur every 2
weeks as a part of the build-up phase. They will continue to updose until they reach
4,000 mg protein daily, which is the maximum maintenance amount of protein. We expect
active OIT treatment subjects to reach 4,000 mg of peanut protein between 44-78 weeks.

Treatment and Desensitization Failures:

A treatment failure will be defined as a) failure to reach 1.5 mg peanut protein (single
dose) during the Initial Dose Escalation Day or b) failure to reach 1,000 mg peanut protein
by week 104.

Subjects who do not meet the criteria at Week 104 and who demonstrate clinical reactivity
will be considered desensitization failures.

If Arm B subjects demonstrate clinical reactivity in any DBPCFC from Week 117 to end of
study, they will be considered desensitization failures.

If Arm A subjects demonstrate clinical reactivity (≥Grade 1, in any DBPCFC from Week 117 to
end of study, they will be considered tolerance failures.

Treatment failures, desensitization failures, and tolerance failures will be unblinded (both
participant and research staff) and will be followed until the end of the study at the
specified study visits but will not undergo DBPCFCs. They will be considered in statistical
analyses of the intent-to-treat population.

Inclusion Criteria:

- Subject and/or parent guardian must be able to understand and provide informed consent
and/or assent as applicable.

- Peanut-allergic subjects between the ages of 8-55 years old.

- Sensitivity to peanut allergen as documented by a positive skin prick test result (5
mm or greater diameter wheal relative to negative control) within 10 months preceding
enrollment.

- Allergy to peanut based on a double-blind placebo-controlled oral food challenge
(DBPCFC) (see Appendix 4 for scoring details) failed at a dose ≤500 mg with peanut
protein within 10 months preceding enrollment.

- All female subjects of child-bearing potential will be required to provide a blood or
urine sample for pregnancy testing that must be negative one week before being allowed
to participate in the study.

- Subjects must plan to remain in the study area during the trial.

- Subjects must be trained on the proper use of the EpiPen (see Appendix 6) to be
allowed to enroll in the study.

- Subjects with other food allergies must agree to eliminate these other food items from
their diet so as not to confound the safety and efficacy data from the study.

- Use of birth control by female subjects of child-bearing potential

Exclusion Criteria:

- Inability or unwillingness of a participant to give written informed consent or comply
with study protocol

- History of cardiovascular disease

- History of other chronic disease (other than asthma, atopic dermatitis, or rhinitis)
requiring therapy (e.g., heart disease, diabetes) that, in the opinion of the
Principal Investigator, would represent a risk to the subject's health or safety in
this study or the subject's ability to comply with the study protocol

- History of eosinophilic gastrointestinal disease

- Current participation in any other interventional study

- Subject is on 'build-up phase" of immunotherapy to another allergen (i.e., has not
reached maintenance dosing)

- Severe asthma (2007 NHLBI Criteria Steps 5 or 6) at time of enrollment

- • Use of complementary and alternative medicine (CAM) treatment modalities (e.g.,
herbal remedies) for atopic and/or non-atopic disease within 90 days preceding Initial
Dose Escalation Day (IDED) or at any time after the IDED

- Inability to discontinue antihistamines for the initial day of escalation, skin
testing or OFCs

- Use of omalizumab within the past six months, or current use of other non-traditional
forms of allergen immunotherapy (e.g., oral or sublingual) or immunomodulator therapy
(not including corticosteroids)

- Use of β-blockers (oral), angiotensin-converting enzyme (ACE) inhibitors,
angiotensin-receptor blockers (ARB) or calcium channel blockers

- Pregnancy or lactation

- History of sensitivity to oat

- History of severe anaphylaxis to peanut with symptoms including hypotension requiring
fluid resuscitation and/or the need for mechanical ventilation

- Use of investigational drugs within 24 weeks of participation

- Past or current medical problems or findings from physical assessment or laboratory
testing that are not listed above, which, in the opinion of the investigator, may pose
additional risks from participation in the study, may interfere with the participant's
ability to comply with study requirements or that may impact the quality or
interpretation of the data obtained from the study.