Last updated: October 17, 2023
Sponsor: Massachusetts General Hospital
Overall Status: Active - Recruiting
Phase
1/2
Condition
Allergy
Allergy (Pediatric)
Allergies & Asthma
Treatment
Placebo plus placebo with PNOIT
Placebo plus VE416 with PNOIT
Vancomycin plus VE416 with PNOIT
Clinical Study ID
NCT03936998
2019P000886
Ages 12-55 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- People of all ethnic/racial/gender groups aged 12-55 years old with a documentedmedical history of peanut allergy.
- Evidence of peanut-specific IgE by either: positive skin prick test to peanut (reaction wheal at least 5 mm larger than saline control) or serum peanut-specific IgE _5 kU/L at screening visit.
- Ara h 2 specific IgE >0.35 kU/L at screening visit.
- Willing to sign informed consent or whose parent or legal guardian is willing to signthe consent form (age appropriate).
- Willing to sign the assent form, if age appropriate.
- (For continuation into Phase II only) Allergic reaction requiring treatment at _ 100mg dose of peanut protein during Entry Challenge.
Exclusion
Exclusion Criteria:
- History of severe anaphylaxis as defined by hypoxia (cyanosis or SpO2 <92% duringreaction), documented hypotension (documented systolic BP >30% below predicted normalfor sex, height, weight or from known baseline), neurological compromise (confusion,loss of consciousness), or incontinence.
- Severe or Moderate asthma as defined using the severity criteria of the current NHLBIGuidelines for the Diagnosis and Management of Asthma (http://www.nhlbi.nih.gov/guidelines/asthma/).
- Poorly-controlled asthma as defined by FEV1 <80% or any of the following symptoms:nighttime awakening >2 days/week or rescue medication use >2 days / week.
- Diagnosis of other severe or complicating medical problems, including autoimmune orchronic immune inflammatory conditions or gastrointestinal inflammatory conditions,including Celiac Disease, Inflammatory Bowel Disease and Eosinophilic GastrointestinalDisorders
- Inability to cooperate with and/or perform oral food challenge procedures.
- Inability to swallow size 0 capsule
- Primary Immune Deficiency
- Allergy to oat confirmed by skin prick testing and history
- Current use of beta blockers, angiotensin converting enzyme inhibitors, or monoamineoxidase inhibitors
- Women of childbearing potential who are pregnant, planning to become pregnant, orbreastfeeding
- Hematocrit <0.36 for adult females or <0.38 for adult males Weight <23 kg
- Use within the past 6 months of other systemic immunomodulatory treatments includingallergen immunotherapy, or use of biologics with an immune target, includingomalizumab.
- Past or current medical problems or findings from physical examination or laboratorytesting that are not listed above, which, in the opinion of the investigator, may poseadditional risks from participation in the study, may interfere with the participant'sability to comply with study requirements or that may impact the quality orinterpretation of the data obtained from the study may also exclude a participant fromthe study.
Study Design
Total Participants: 60
Treatment Group(s): 4
Primary Treatment: Placebo plus placebo with PNOIT
Phase: 1/2
Study Start date:
June 28, 2019
Estimated Completion Date:
January 01, 2024
Study Description
Connect with a study center
Massachusetts General Hospital
Boston, Massachusetts 02114
United StatesActive - Recruiting
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