- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01814241
Mechanisms of Desensitization During Peanut Oral Immunotherapy (PnOIT4)
27. februar 2018 opdateret af: University of North Carolina, Chapel Hill
The purpose of this study is to attempt to understand how desensitization works in peanut allergic children who are undergoing oral immunotherapy (OIT) to peanut.
We want to identify the early changes in the desensitization process the immune cells undergo to become desensitized to the peanut protein.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Peanut allergic children will undergo an oral food challenge (OFC) to 1 gm peanut protein in order to accomplish two objectives: (1)to confirm the diagnosis of peanut allergy, and (2) to measure the amount of peanut protein it takes to cause an allergic reaction.
Each subject will then undergo a modified rush phase in which the subject receives 6 doses of peanut protein in one day.
The build-up phase begins afterward in which the subject's dose of peanut protein is increased every 2 weeks for 36 weeks.
After the final build-up dose, the subject consumes that dose for 2 weeks after which he or she returns to the food allergy center for the second food challenge.
If the subject successfully consumes this food challenge without symptoms, the daily dosing of peanut protein will be stopped and the subject will then undergo a third food challenge.
If the subject successfully consumes the peanut protein during that challenge, he or she will return for a fourth food challenge to peanut.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
20
Fase
- Fase 2
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
North Carolina
-
Chapel Hill, North Carolina, Forenede Stater, 27599
- UNC Chapel Hill
-
-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
4 år til 12 år (Barn)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Age 4 to up to 12 years of age of any gender, race, or ethnicity.
- Minimum weight 16 kg at the time of enrollment.
- Physician diagnosis of peanut allergy OR convincing clinical history of an allergic reaction to peanut.
- Detectable serum peanut -specific IgE level (CAP-FEIA ≥ 0.35 kU/L) and a positive SPT (wheal ≥ 3mm on skin prick test to peanut extract compared to a negative control.)
- Allergic reaction to ≤ 1 gm peanut protein during a blinded oral challenge test conducted at screening (e.g., a double-blinded, placebo-controlled food challenge [DBPCFC]).
- Written informed consent from parent/guardian.
- Written assent from subject if applicable
- Consumption of oat-containing product within 90 days prior to enrollment
Exclusion Criteria:
- History of allergic reaction to peanut consistent with severe anaphylaxis (defined as hypotension/shock; or neurologic impairment).
- Chronic disease other than asthma, atopic dermatitis, rhinitis requiring therapy; e.g., heart disease or diabetes.
- Active eosinophilic gastrointestinal disease in the past 2 years
- Participation in any interventional study for the treatment of food allergy in the 6 months prior to visit -1
- Inhalant allergen immunotherapy that has not yet reached maintenance dosing.
- Asthma defined as moderate or severe persistent by National Asthma Education and Prevention Program Expert Panel Guidelines (e.g. asthma that requires more than fluticasone 440 mcg or its equivalent daily for adequate control).
- Inability to discontinue antihistamines for skin testing, OFC and the initial dose escalation.
- Use of omalizumab or other non-traditional forms of allergen immunotherapy (e.g., oral or sublingual) in the 12 months prior to visit -1.
- Any systemic therapy which in the judgment of the investigator could be immunomodulatory (e.g. rituximab) in the 12 months prior to visit -1, Systemic corticosteroid therapy of up to a total of three weeks is allowed.
- Use of investigational drug in 90 days prior to visit -1.
- Plan to use any investigational drug during the study period.
- The presence of any medical condition that the investigator deems incompatible with participation in the trial.
- Inability to speak English.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Andet
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Open label peanut OIT
Open label orally ingested peanut flour with maintenance dose of 1450mg
|
Subject will take increasing amounts of peanut protein up to a maximum maintenace dose of 1450mg.
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Percentage of Subjects Who Develop Desensitization
Tidsramme: 40 weeks
|
The percentage of peanut allergic subjects who develop desensitization as defined by being able to consume 5000mg of peanut protein during a double blind food challenge after completing a build-up phase of peanut OIT.
|
40 weeks
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Percentage of Subjects Who Maintain Desensitization Once OIT is Stopped
Tidsramme: 4 weeks
|
The percentage of subjects who maintain desensitization once the OIT is withdrawn at 1, 2, 3, and 4 week intervals.
|
4 weeks
|
Andre resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Change From Baseline in the Wheal Diameter, as Assessed by the Skin Prick Test (SPT) to Peanut
Tidsramme: 44 weeks
|
Allergic reactivity of mast cells is assessed by skin prick testing through measurement of the wheal diameter after exposure to peanut.
This outcome measure reports the change in skin prick test wheal diameter from baseline through the end of the treatment period.
|
44 weeks
|
|
Change in Peanut Specific Immunoglobin E (IgE) From Baseline Until Desensitization Food Challenge
Tidsramme: 44 weeks
|
The investigation of mechanistic changes that occur in the immune system over the duration of the study - Peanut specific immunoglobin E (IgE)
|
44 weeks
|
|
Change in Immunoglobin G4 (IgG4) to Peanut From Baseline Until Desensitization Food Challenge
Tidsramme: 44 weeks
|
The investigation of mechanistic changes that occur in the immune system dover the duration of the study - Immunoglobin G4 (IgG4) to peanut
|
44 weeks
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Wesley Burks, MD, UNC Chapel Hill
- Ledende efterforsker: Edwin Kim, MD, UNC Chapel Hill
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart
1. april 2013
Primær færdiggørelse (Faktiske)
1. december 2015
Studieafslutning (Faktiske)
1. december 2015
Datoer for studieregistrering
Først indsendt
15. marts 2013
Først indsendt, der opfyldte QC-kriterier
15. marts 2013
Først opslået (Skøn)
19. marts 2013
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
1. marts 2018
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
27. februar 2018
Sidst verificeret
1. marts 2017
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 13-0900
- R01AI068074 (U.S. NIH-bevilling/kontrakt)
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
INGEN
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