Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:23 AM
Ignite Modification Date:
2025-12-25 @ 4:23 AM
NCT ID:
NCT03648320
Eligibility Criteria:
Inclusion Criteria:
For peanut OIT patients:
Adults aged 18-40 years with:
1. A positive skin prick test to peanut extract.
2. Elevated (\>0.35) serum specific Immunoglobulin E (IgE) to Ara h 2 major peanut allergen within 2 years of date of initial screening visit.
3. Positive DBPCFC to 300mg or less of peanut protein.
4. Where appropriate, use of effective form of birth control by females for the duration of participation in the study (i.e. up to exit DBPCFC).
5. Participants with asthma may be included if well controlled:
* Asthma control questionnaire (ACQ) score \<1
* Maximum permitted asthma treatment: moderate dose of inhaled corticosteroid (ICS) and long-acting beta agonists (LABA) as treatment
* Pre-bronchodilator Forced Expiratory Volume in 1 second (FEV1) \>80% of predicted value at screening visit
* For asthmatic participants with intermittent mild symptoms (induced by exercise, animals or pollens) using as required salbutamol only, treatment will be given with regular low dose inhaled corticosteroids (ICS) prior to challenges and for the duration of updosing as an additional measure.
For mechanistic sub-study subjects:
Adults aged 18-40 years with:
1. A positive skin prick test to peanut extract within previous 12 months
2. Elevated serum specific IgE (\>0.35) to Ara h 2 major peanut allergen within 2 years of date of initial screening visit.
3. Clinical diagnosis of peanut allergy made by an experienced allergy specialist.
Exclusion Criteria:
For peanut OIT patients:
1. Anaphylaxis to a food other than peanut - despite attempted avoidance - within the last 2 years.
2. History of life-threatening anaphylaxis or angioedema, including previous intensive care unit (ITU) admission attributable peanut allergy.
3. Asthmatic treated with higher than moderate dose of ICS (\>800 mcg equivalent of beclomethasone dipropionate (BDP) per day).
4. Any asthmatic if uncontrolled or difficult to control as evidenced by any following: ACQ\>1; FEV1 \<80% predicted; FEV1/ forced vital capacity (FVC) \<0.7 irrespective of treatment; hospital attendance (A\&E or admission) for asthma in the past 2 years; treatment of asthma with oral steroids within last 2 years.
5. Evidence of non-adherence with asthma treatment from General PRactitioner (GP) repeat prescription records.
6. Participants who react to less than 1 mg of peanut protein on DBPCFC, or who cannot tolerate at least an initial dose of 1.5 mg peanut protein on OIT initiation day.
7. Participants who react to placebo during DBPCFC.
8. Ongoing treatment with beta-blockers, biologics (such as omalizumab or mepolizumab) or systemic immunosuppressive treatment.
9. Regular ongoing use of NSAIDs for a chronic condition (NSAIDs may act as a co-factor for allergic reactions)
10. For females a positive serum or urine pregnancy test with sensitivity of less than 50 mIU/mL within 72 hours of first administration of study therapy.
11. Lactating females.
12. The use of any investigational drug within 30 days of the screening visit.
13. Past history of eosinophilic oesophagitis or chronic gastro-oesophageal reflux symptoms requiring regular treatment with anti-acids.
14. Inability to discontinue antihistamines for a minimum of 4 days prior to DBPCFC visits
15. The presence of any medical condition that the investigator deems incompatible with participation in the trial.
16. Individuals with insufficient understanding of the trial.
For mechanistic sub-study subjects:
1. Ongoing treatment with biologic or systemic immunosuppressive treatment.
2. Known current pregnancy
3. Lactating females.
4. The use of any investigational drug within 30 days of the screening visit.
5. Inability to discontinue antihistamines for a minimum of 4 days prior to venesection.
6. The presence of any medical condition that the investigator deems incompatible with participation in the study.
7. Individuals with insufficient understanding of the study.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
40 Years
Study:
NCT03648320
Study Brief:
Protocol Section:
NCT03648320