For Healthcare Professionals

Peanut Sublingual Immunotherapy (SLIT)-Tablet for Treatment of Peanut Allergy

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About the study

This clinical research study investigates the safety and tolerability of a peanut SLIT-tablet.
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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:

  1. Part 1: Male or female aged 12 through 65 years (inclusive) on the day of enrollment
  2. Part 2: Male or female aged 4 through 65 years (inclusive) on the day of enrollment
  3. Documented clinical history of an IgE-mediated allergic reaction towards peanut- containing food
  4. Peanut-specific serum IgE ≥ 0.7 kUA/L at screening measured at central laboratory
  5. Skin prick test to peanut ≥ 5 mm at screening
  6. 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
  7. 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:

  1. Diagnosis or history of eosinophilic esophagitis
  2. 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)
  3. Part 1 and 2: All subjects ≥ 5 years old with FEV1 or PEFR < 70% of predicted value at enrollment
  4. 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
  5. Up-dosing with any allergy immunotherapy product. Maintenance dose of any subcutaneous immunotherapy product other than peanut is allowed
  6. History of peanut oral immunotherapy within the last 12 months prior to visit 1
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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall +45 45747576Email iconEmail Study Center

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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