Peanut Sublingual Immunotherapy (SLIT)-Tablet for Treatment of Peanut Allergy
About the study
This clinical research study investigates the safety and tolerability of a peanut SLIT-tablet.
Who can take part
You may be eligible to participate in the study if you meet the following criteria:
INCLUSION CRITERIA
Inclusion criteria apply to both part 1 and part 2 of the trial, unless otherwise specified.
EXCLUSION CRITERIA
Subjects are eligible to be included in the trial only if all the following criteria apply:
- Part 1: Male or female aged 12 through 65 years (inclusive) on the day of enrollment
- Part 2: Male or female aged 4 through 65 years (inclusive) on the day of enrollment
- Documented clinical history of an IgE-mediated allergic reaction towards peanut- containing food
- Peanut-specific serum IgE ≥ 0.7 kUA/L at screening measured at central laboratory
- Skin prick test to peanut ≥ 5 mm at screening
- Cohorts 1-8: Experience dose-limiting symptoms at the 10 mg, 30 mg or 100 mg challenge dose of peanut protein on screening double-blind, placebo-controlled food challenge
- Cohorts 9-10: Experience dose-limiting symptoms at the 1 mg or 3 mg challenge dose of peanut protein on the screening double-blind, placebo-controlled food challenge
Subjects are excluded from the trial if any of the following criteria apply:
- Diagnosis or history of eosinophilic esophagitis
- Uncontrolled asthma as defined by the Asthma Control Test questionnaire with a score of 19 or below at enrollment (subjects with a diagnosis of asthma only)
- Part 1 and 2: All subjects ≥ 5 years old with FEV1 or PEFR < 70% of predicted value at enrollment
- Part 2: Subjects 4 years old with a history of recurrent wheeze requiring inhaled corticosteroids for 2 consecutive weeks or more within 3 months prior to enrollment
- Up-dosing with any allergy immunotherapy product. Maintenance dose of any subcutaneous immunotherapy product other than peanut is allowed
- History of peanut oral immunotherapy within the last 12 months prior to visit 1
Study Locations
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How to Apply
Contact the study center to learn if this study is a good match for you.
Study’s details
Contition
Peanut Allergy
Age (in years)
4 - 65
Phase
Phase 1
Participants needed
90
Est. Completion Date
Nov 30, 2024
Treatment type
Interventional
Sponsor
ALK-Abelló A/S
ClinicalTrials.gov identifier
NCT05440643
Study number
PT-01
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