Home › Peanut Hypersensitivity › NCT03936998
VE416 for Treatment of Food Allergy
RecruitingPhase 1/2
VE416 and Low-dose Peanut Oral Immunotherapy for Treatment of Persistent Peanut Allergy
Who can join
Ages 12 to 55 · All sexes
Full eligibility criteria
Inclusion Criteria: * People of all ethnic/racial/gender groups aged 12-55 years old with a documented medical 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 sign the consent form (age appropriate). * Willing to sign the assent form, if age appropriate. * (For continuation into Phase II only) Allergic reaction requiring treatment at \_ 100 mg dose of peanut protein during Entry Challenge. Exclusion Criteria: * History of severe anaphylaxis as defined by hypoxia (cyanosis or SpO2 \<92% during reaction), documented hypotension (documented systolic BP \>30% below predicted normal for 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 NHLBI Guidelines 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 or chronic immune inflammatory conditions or gastrointestinal inflammatory conditions, including Celiac Disease, Inflammatory Bowel Disease and Eosinophilic Gastrointestinal Disorders * 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 monoamine oxidase inhibitors * Women of childbearing potential who are pregnant, planning to become pregnant, or breastfeeding * 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 including allergen immunotherapy, or use of biologics with an immune target, including omalizumab. * Past or current medical problems or findings from physical examination or laboratory testing that are not listed above, which, in the opinion of the investigator, may pose additional risks from participation in the study, may interfere with the participant's ability to comply with study requirements or that may impact the quality or interpretation of the data obtained from the study may also exclude a participant from the study.
About the study
This is a single-center, randomized, double-blind trial with four arms evaluating VE416 as pretreatment or concurrent treatment in comparison to low-dose peanut oral immunotherapy (PNOIT) alone.
What is being tested
- Vancomycin plus VE416 before PNOIT (combination product)
- Vancomycin plus VE416 with PNOIT (combination product)
- Placebo plus VE416 with PNOIT (combination product)
- Placebo plus placebo with PNOIT (combination product)
Sponsor: Massachusetts General Hospital · Participants: 60 · Started: Jun 28, 2019
Contact the study team
- Wayne G Shreffler, MD, PhD · Phone: 617-726-6147
- Jannat Gill, BDS, MPH · Phone: 617-643-8683
Official record on ClinicalTrials.gov — NCT03936998
Locations in the U.S.
| Massachusetts | Massachusetts General Hospital, Boston |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.