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Completed

NCT Number: NCT04090203

Boiled Peanut Oral Immunotherapy

Prospective Phase 1 clinical trial providing proof of concept data on boiled peanut oral immunotherapy (OIT) for the treatment of peanut allergy in children. The investigators hypothesize that the proportion of subjects successfully desensitized with boiled peanut OIT is greater than the theoretical placebo rate of 20%.

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Key information

Age range

1 year–16 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Cleveland Clinic Foundation

Cleveland, Ohio, 44195, United States

About this study

Oral Immunotherapy will be administered utilizing a powder derived from boiled peanuts. Treatment will begin with an initial escalation day in which dosing is begun at 0.1 mg peanut protein and escalated to a final dose of 6 mg peanut protein. Doses are ingested orally. Participants will continue daily oral ingestion of doses at home and return for updosing every 2 weeks to a final maintenance dose of 300 mg peanut protein. Participants will continue daily oral ingestion of the peanut product for a minimum duration of 28 days before undergoing exit double blind placebo controlled food challenge. At the conclusion of the study, participants will be offered continued maintenance therapy off study in line with current specialty standards.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 1-16 years
  • History of immediate hypersensitivity reaction to peanut
  • Evidence of IgE mediated peanut hypersensitivity within a 12 month period of study enrollment
  • SPT with wheal/flare of at least 3 x 6 mm and/or Peanut specific IgE >0.35 kU/L

Exclusion criteria

  • History of life threatening peanut anaphylaxis
  • Asthma requiring more than medium dose ICS
  • Prior participation in oral immunotherapy, sublingual immunotherapy or epicutaneous immunotherapy
  • Oat allergy
  • Cardiovascular Disease
  • Use of beta-blockers (oral), angiotensin converting enzyme inhibitors, angiotensin receptor blockers, or calcium channel blockers
  • Use of steroid medications in the following manners:
  • Daily oral steroid dosing for greater than 1 month during the past year
  • Burst or steroid course in the past 3 month before inclusion
  • Greater than 2 bursts oral steroid courses in the past year of at least 1 week duration
  • Pregnancy or lactation
  • Eosinophilic Gastrointestinal Disease
  • History of food protein-induced enterocolitis
  • History of developmental delay or speech delay that precludes age- appropriate communication, in the opinion of the investigator

Treatment and study plan

Boiled Peanut Powder

Drug

Oral Immunotherapy will be administered utilizing a powder derived from boiled peanuts. Treatment will begin with an initial escalation day in which dosing is begun at 0.1 mg peanut protein and escalated to a final dose of 6 mg peanut protein. Doses are ingested orally. The subjects will continue daily oral ingestion of doses at home and return for updosing every 2 weeks to a final maintenance dose of 300 mg peanut protein. The subjects will continue daily oral ingestion of the peanut product for a minimum duration of 28 days before undergoing exit DBPCFC. At the conclusion of the study, patients will be offered continued maintenance therapy off study in line with current specialty standards.

Other names: Immunotherapy

Primary outcomes

  1. Increase in Tolerance to Peanut in Pediatric Patients With Peanut Hypersensitivity Reported as the Percentage of Participants Successfully Desensitized.

    Time frame: 18 weeks

    The percentage of patients able to consume a single dose of 300 mg or greater of peanut protein with no dose limiting symptoms at exit food challenge are considered 'successfully desensitized'. Any enrolled participants who did not tolerate the 300 mg dose or did not complete the exit food challenge for any reason are considered not successfully desensitized. The percentage of successfully desensitized participants is presented with corresponding lower bound of the one-sided 95% CI, calculated as the lower bound of a two-sided 90% exact confidence interval.

Sponsors and collaborators

Lead sponsor

Alton Melton

Other

Collaborators

  • The Cleveland Clinic

Registry information

Official study title

Boiled Peanut Oral Immunotherapy for the Treatment of Peanut Allergic Pediatric Patients

Acronym: BPOIT

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Sep 16, 2019
Registry last updated
Sep 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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