High and Low Dose Oral Sesame Immunotherapy - Comparison of Efficacy and Safety (Sesame)
Primary Purpose
Food Allergy
Status
Recruiting
Phase
Not Applicable
Locations
Poland
Study Type
Interventional
Intervention
High dose
Low dose
Sponsored by
About this trial
This is an interventional treatment trial for Food Allergy focused on measuring sesame, food allergy, immunotherapy, children
Eligibility Criteria
Inclusion Criteria:
- medical history of sesame allergy,
- IgE-mediated sesame allergy confirmed as positive skin prick tests with sesame allergens (diameter of the wheal greater than 3mm) and/or specific IgE level greater than 0.35 kilo units of Allergen per liter (kUA/l) (UniCAP method),
- reaction to sesame protein during OOFC (maximum dose 4000g),
- signed Informed Consent by parent/legal guardian and patient aged >16 years old,
- patient's/caregivers' cooperation with researcher.
Exclusion Criteria:
- no confirmed sesame allergy,
- negative oral food challenge with sesame protein (maximum dose 4000g),
- severe asthma,
- uncontrolled mild/moderate asthma: forced expiratory volume at one second (FEV1)<80% (under 5. percentile), FEV1/forced vital capacity (FVC)<75% (under 5. percentile), hospitalization due to asthma exacerbation within last 12 months,
- current oral/sublingual/subcutaneous immunotherapy with other allergen,
- eosinophilic gastroenteritis,
- a history of severe recurrent anaphylaxis episodes,
- chronic diseases requiring continuous treatment, including heart disease, epilepsy, metabolic diseases, diabetes,
medication:
- oral, daily steroid therapy longer than 1 month within last 12 months,
- at least two courses of oral steroid therapy (at least 7 days) within last 12 months,
- oral steroid therapy longer than 7 days within last 3 months,
- biological treatment,
- the need to constantly take antihistamines,
- therapy with β-blockers, angiotensin converting enzyme (ACE) inhibitors, calcium channel inhibitors,
- pregnancy,
- no consent to participate in the study,
- lack of patient cooperation.
Sites / Locations
- Katarzyna GrzelaRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
High dose
Low dose
Arm Description
Experimental: high dose of sesame 20 patients
Active Comparator: low dose of sesame 20 patients
Outcomes
Primary Outcome Measures
Tolerance of sesame
Proportion of participants who tolerate the single dose of 4000mg sesame protein
Secondary Outcome Measures
Adverse event
Quantity and severity of adverse effect, assessed and compared between groups, divided into mild, moderate and severe category
Laboratory data
Difference in sesame serum immunoglobulin E (IgE) level and immunoglobulin G4 (IgG4) level, compared between groups at the end of treatment
Basophil activation test
The basophil activation test (BAT) results compared between groups at the end of treatment
Skin prick test (SPT)
Change in skin prick test reactivity to sesame protein from baseline to end of treatment, compared between groups
Desensitization dose
Change in maximum tolerated dose of sesame in oral food challenge before and in the end of treatment, compared between groups
Full Information
NCT ID
NCT05158413
First Posted
November 24, 2021
Last Updated
December 5, 2022
Sponsor
Medical University of Warsaw
1. Study Identification
Unique Protocol Identification Number
NCT05158413
Brief Title
High and Low Dose Oral Sesame Immunotherapy - Comparison of Efficacy and Safety
Acronym
Sesame
Official Title
High and Low Dose Oral Sesame Immunotherapy - Comparison of Efficacy and Safety
Study Type
Interventional
2. Study Status
Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 31, 2022 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
June 30, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medical University of Warsaw
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
In this trial the investigators aim to assess the effectiveness and safety of oral immunotherapy with sesame protein in high and low dose (300mg versus 1200mg) in children with sesame allergy.
Detailed Description
Sesame allergy is an important global clinical problem affecting 0,2-0,8% population. In food allergy, allergen avoidance and emergency treatment are still therapeutic hallmarks. Oral and sublingual allergen-specific immunotherapies have been provided as a new approach to managing food allergy. The main goal of oral immunotherapy is to obtain the desensitization to food. The oral immunotherapy (OIT) is considered as safe and highly effective, according to current research. In addition, this type of therapy reduce the influence of food allergy in patient's live.
Children 4 to 17 years old with sesame allergy will be enrolled into study. Skin prick test with condiment made from toasted ground hulled sesame and open oral food challenge (OOFC) will be performed at the baseline and at the end of procedure. Blood will be analyzed for specific IgE, IgG4 levels and basophil activation test before and after OIT. OIT will consisted of two parts: dosage increase phase and maintenance phase. The Participants will be randomized (1:1) to receive sesame OIT with maintenance dose of 300 mg or 1200 mg sesame protein.
In the dosage increase phase, the dose of condiment made from toasted ground hulled sesame will be gradually increased every two weeks and administrated to a child during hospitalization (1-day procedure). Precondition to increase of dose is good tolerance of previous portion of condiment made from toasted ground hulled sesame. The maximum time frame for this phase is 14 months.
After achieving tolerance, immunotherapy will be continued for 3 months in maintenance phase, with dose 300mg or 1200 mg sesame protein. Maintenance dose is determined by random patients' assignment to one from study's .
After 3 months (12 weeks +/-2 weeks) of maintenance dose the final OOFC and evaluation of desensitization of sesame protein will be performed. Confirmation of the total desensitization to sesame is the tolerance of a single dose of 4000 mg sesame protein.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Food Allergy
Keywords
sesame, food allergy, immunotherapy, children
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomly assigned to two groups. During the maintenance phase, the first group will receive low dose of sesame protein, which amounts 300mg, the second will get high dose, which is 1200 mg of sesame protein. Oral immunotherapy with low (300mg) and high (1200mg) dose of sesame protein in children randomly assigned to two groups (1:1). Patients will receive ground sesame mixed with apple mousse (supposing apple tolerance). For the transparency of the study all patients will receive the same commercially prepared apple muss product.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
High dose
Arm Type
Experimental
Arm Description
Experimental: high dose of sesame 20 patients
Arm Title
Low dose
Arm Type
Active Comparator
Arm Description
Active Comparator: low dose of sesame 20 patients
Intervention Type
Dietary Supplement
Intervention Name(s)
High dose
Intervention Description
Patients will receive a high dose of sesame paste or flour (1200 mg of sesame protein) mixed with apple mousse (supposing child tolerates apple). For the transparency of the study all patients will receive the same commercially prepared apple product
Intervention Type
Dietary Supplement
Intervention Name(s)
Low dose
Intervention Description
Patients will receive a low dose of sesame paste or flour (300 mg of sesame protein) mixed with apple mousse (supposing child tolerates apple). For the transparency of the study all patients will receive the same commercially prepared apple product
Primary Outcome Measure Information:
Title
Tolerance of sesame
Description
Proportion of participants who tolerate the single dose of 4000mg sesame protein
Time Frame
Up to 16 months after starting oral immunotherapy
Secondary Outcome Measure Information:
Title
Adverse event
Description
Quantity and severity of adverse effect, assessed and compared between groups, divided into mild, moderate and severe category
Time Frame
Up to 16 months after starting oral immunotherapy
Title
Laboratory data
Description
Difference in sesame serum immunoglobulin E (IgE) level and immunoglobulin G4 (IgG4) level, compared between groups at the end of treatment
Time Frame
Up to 16 months after starting oral immunotherapy
Title
Basophil activation test
Description
The basophil activation test (BAT) results compared between groups at the end of treatment
Time Frame
Up to 16 months after starting oral immunotherapy
Title
Skin prick test (SPT)
Description
Change in skin prick test reactivity to sesame protein from baseline to end of treatment, compared between groups
Time Frame
Up to 16 months after starting oral immunotherapy
Title
Desensitization dose
Description
Change in maximum tolerated dose of sesame in oral food challenge before and in the end of treatment, compared between groups
Time Frame
Up to 16 months after starting oral immunotherapy
10. Eligibility
Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
17 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
medical history of sesame allergy,
IgE-mediated sesame allergy confirmed as positive skin prick tests with sesame allergens (diameter of the wheal greater than 3mm) and/or specific IgE level greater than 0.35 kilo units of Allergen per liter (kUA/l) (UniCAP method),
reaction to sesame protein during OOFC (maximum dose 4000g),
signed Informed Consent by parent/legal guardian and patient aged >16 years old,
patient's/caregivers' cooperation with researcher.
Exclusion Criteria:
no confirmed sesame allergy,
negative oral food challenge with sesame protein (maximum dose 4000g),
severe asthma,
uncontrolled mild/moderate asthma: forced expiratory volume at one second (FEV1)<80% (under 5. percentile), FEV1/forced vital capacity (FVC)<75% (under 5. percentile), hospitalization due to asthma exacerbation within last 12 months,
current oral/sublingual/subcutaneous immunotherapy with other allergen,
eosinophilic gastroenteritis,
a history of severe recurrent anaphylaxis episodes,
chronic diseases requiring continuous treatment, including heart disease, epilepsy, metabolic diseases, diabetes,
medication:
oral, daily steroid therapy longer than 1 month within last 12 months,
at least two courses of oral steroid therapy (at least 7 days) within last 12 months,
oral steroid therapy longer than 7 days within last 3 months,
biological treatment,
the need to constantly take antihistamines,
therapy with β-blockers, angiotensin converting enzyme (ACE) inhibitors, calcium channel inhibitors,
pregnancy,
no consent to participate in the study,
lack of patient cooperation.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Katarzyna Grzela, MD, PhD
Phone
+48 22 3179431
Email
katarzyna.grzela@wum.edu.pl
First Name & Middle Initial & Last Name or Official Title & Degree
Joanna Zielińska, MD
Email
joanna_zielinska@outlook.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Katarzyna Grzela, MD, PhD
Organizational Affiliation
Medical University of Warsaw
Official's Role
Study Chair
Facility Information:
Facility Name
Katarzyna Grzela
City
Warsaw
ZIP/Postal Code
02-091
Country
Poland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Katarzyna Grzela, PhD, MD
Phone
+48223179431
Email
katarzyna.grzela@wum.edu.pl
First Name & Middle Initial & Last Name & Degree
Joanna Zielińska, MD
Email
joanna_zielinska@outlook.com
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
30819972
Citation
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Results Reference
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PubMed Identifier
30646188
Citation
Gupta RS, Warren CM, Smith BM, Jiang J, Blumenstock JA, Davis MM, Schleimer RP, Nadeau KC. Prevalence and Severity of Food Allergies Among US Adults. JAMA Netw Open. 2019 Jan 4;2(1):e185630. doi: 10.1001/jamanetworkopen.2018.5630.
Results Reference
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PubMed Identifier
22610362
Citation
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PubMed Identifier
31373655
Citation
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Results Reference
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PubMed Identifier
31150789
Citation
Nachshon L, Goldberg MR, Levy MB, Appel MY, Epstein-Rigbi N, Lidholm J, Holmqvist M, Katz Y, Elizur A. Efficacy and Safety of Sesame Oral Immunotherapy-A Real-World, Single-Center Study. J Allergy Clin Immunol Pract. 2019 Nov-Dec;7(8):2775-2781.e2. doi: 10.1016/j.jaip.2019.05.031. Epub 2019 May 29.
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High and Low Dose Oral Sesame Immunotherapy - Comparison of Efficacy and Safety
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