Therapeutic Effect of Chinese Herbal Medicine on Food Allergy

To address our hypothesis, we propose the following aims:

Aim #1: To investigate the efficacy of FAHF-2TM for food allergy (in addition to current
food allergen avoidance).

Aim #2: To characterize the immunomodulatory effects of FAHF-2TM on food allergic patients

Inclusion Criteria:

- Male and female subjects ages 12 through 45 years of age and otherwise in good health
as determined by medical history and physical examination

- History of allergy to peanut, tree nut, sesame, fish or shellfish as documented by a
positive skin test and/or food allergen-specific IgE level.

- The subject agrees to participate in the study or the subject's parent or legal
guardian is willing and able to give written informed consent, and the pediatric
subject gives assent for participation in the study.

- Positive double-blind placebo controlled food challenge to peanut, tree nuts, sesame,
fish, or shellfish.

- Females of childbearing potential must be inactive sexually or take effective birth
control measures, as deemed appropriate by the investigator, for the duration of the
study

Exclusion Criteria:

- History of life-threatening anaphylaxis to peanut, tree nut, sesame, fish or
shellfish (involving hypotension or requiring mechanical ventilation)

- Allergy to corn

- Acute febrile illness (such as cold, flu, etc.) within one week before administration
of study drug

- Any history of systemic disease that in the investigator's opinion would preclude the
subject from participating in this study, e.g. autoimmune disease, neoplasms, HIV or
hepatitis virus infection

- Allergic gastrointestinal disease (e.g. allergic eosinophilic
esophagitis/gastroenteritis

- Abnormal hepatic function (ALT/AST and bilirubin >1.25 x upper limit of normal)

- Abnormal bone marrow function (WBC <4 x 103/mm3; platelets <100 x 103/mm3; hgb <11
g/dl)

- Abnormal renal function (BUN and creatinine >1.25 x upper limit of normal)

- Clinically significant abnormal electrocardiogram

- Current uncontrolled moderate to severe asthma as defined by:

1. FEV1 value <80% predicted or any clinical features of moderate or severe
persistent asthma baseline severity (as defined by the 2007 NHLBI Guidelines)
and greater than high daily doses of inhaled corticosteroids (as defined for
children and adults using dosing tables from the 2007 NHLBI Guidelines).

2. Use of steroid medications in the following manners: history of daily oral
steroid dosing for >1 month during the past year, or burst or steroid course in
the past 6 months, or >1 burst oral steroid course in the past year.

3. Asthma requiring >1 hospitalization in the past year for asthma or >1 ED visit
in the past 6 months for asthma.

- Participation in another experimental therapy study within 30 days of this study

- History of alcohol or drug abuse

- Currently taking antidepressant medication

- Pregnant or lactating female subjects. Females of childbearing potential will need a
negative serum pregnancy test at screening to be considered for this study

- Use of omalizumab

- Use of beta blockers, ACE inhibitors, ARB, or calcium channel blockers, or history of
ischemic heart disease

- Inability to discontinue use of antihistamines for skin testing or oral food
challenges

- Inability to take the tablets