Epicutaneous Immunotherapy in Peanut Allergy in Children

NCT ID: NCT01197053

Last Updated: 2015-10-20

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-08-31
• Study Completion Date: 2015-04-30

Brief Summary

This study aims at showing that Epicutaneous Immunotherapy with peanut proteins is safe and efficacious for desensitizing children with peanut allergy.

Detailed Description

Peanut allergy is a common allergy in the United Sates, with prevalence in the general population as high as 1%. Peanut allergy starts in childhood, its prevalence in children has doubled in the past 5 years, and barely 20% of the allergic children will outgrow this allergy So far, the only treatments available for peanut allergy are avoidance of peanut and injectable epinephrine after the allergic systemic reactions have started. Immunotherapy methods currently available have shown some limitations in their use because of important safety issues. Hence, there is an important unmet medical need for efficient and safe treatment of peanut allergy.

DBV Technologies, is a French biotech company which has developed an Epicutaneous Delivery System, called Viaskin®, a method based on delivering precise quantity of allergens on the upper layers of the skin, i.e. on the epidermis and without any passage in the vascularised dermis. Avoiding contact between the allergens and the bloodstream should confer to epicutaneous immunotherapy (EPIT) a high level of safety as systemic reactions are circumvented.

The goal of this pilot study is to demonstrate that epicutaneous immunotherapy (EPIT) with Viaskin® is safe and efficacious for the desensitization of peanut-allergic children, i.e. increasing the quantity of peanut proteins they can consume symptom-free.

Fifty-two (52) children from 5 to 17 years of age with a confirmed peanut allergy during a baseline double blind placebo-controlled food challenge (DBPCFC) (reacting to a capped value below 250 mg of peanut proteins) will be randomized 1 to 1 and treated either with DBV712, the Viaskin® disk loaded with 100 mcg peanut proteins (active treatment), or with placebo, the Viaskin® disk loaded with a placebo formulation devoid of peanut. Each child will receive one application of one Viaskin® on the skin every day repeatedly for 6 months in a blinded manner, followed by a 12-month open treatment with DBV712 for all of them; placebo children will all cross-over after the first 6 months of treatment to also receive the active treatment.

A DBPCFC to peanut will then be conducted after every 6 months of treatment to assess the efficacy of the treatment. Safety will be assessed during the whole study period.

Skin testing, peanut-specific IgE and IgG4 will occur at selected visits

Conditions

Peanut Allergy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

100 mcg DBV712 (active)

100 mcg DBV712 administered epicutaneously every 24 hours.

Group Type: EXPERIMENTAL

Epicutaneous Immunotherapy

Intervention Type: BIOLOGICAL

100 mcg peanut proteins (active arm) applied on the skin every 24 hrs for 6 months blinded, followed by 12 months open treatment for all patients in the active arm

Placebo

Placebo will be administered epicutaneously every 24 hours

Group Type: PLACEBO_COMPARATOR

placebo of peanut

Intervention Type: BIOLOGICAL

placebo applied on the skin every 24 hrs for 6 months blinded, followed by 12 months open treatment for all patients in the active arm

Interventions

Epicutaneous Immunotherapy

100 mcg peanut proteins (active arm) applied on the skin every 24 hrs for 6 months blinded, followed by 12 months open treatment for all patients in the active arm

Intervention Type: BIOLOGICAL

placebo of peanut

placebo applied on the skin every 24 hrs for 6 months blinded, followed by 12 months open treatment for all patients in the active arm

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

• Male or Female between 5 and 17 years of age at enrollment
• An efficient contraceptive method for girls with childbearing potential. Acceptable methods include sexual abstinence, oral, injectable contraceptive methods, intra uterine device.
• Negative pregnancy test for girls with childbearing potential.
• Child with a documented allergy to peanut, i.e. with peanut-specific IgE (>5KU/L, ImmunoCAP method) and/or a positive skin prick test to peanut (wheal diameter ≥ 8mm).
• Child able to consume a cumulated quantity of peanut proteins <250 mg during the baseline DBPCFC.
• Child and his/her legal representative(s) who provide a signed consent form and assent form.
• Child and his/her legal representative(s) whose family and social conditions allow them to understand the protocol and agree to comply in the long term with all study requirements.

Exclusion Criteria

• Child considered too severely allergic to peanut: with a history of severe anaphylaxis to peanut (with hypotension, loss of consciousness, severe bradycardia, respiratory or cardiac arrest requiring an admission to emergency rooms).
• Child with peanut-specific IgE<5 KU/L and whose skin prick test to peanut gave a wheal diameter <8mm).
• Child participating or having participated in a therapeutic study in the last 3 months
• Pregnancy or Breastfeeding
• Child with a generalized eczema
• Child with an immune deficiency
• Diabetic child
• Child allergic to chocolate
• Child or legal representative(s) who did not sign their consent or assent
• Child with no baseline DBPCFC
• Child having reacted to placebo during the baseline DBPCFC
• Child able to consume > 250 mg of cumulated peanut proteins during the baseline DBPCFC
• Child with a respiratory deficiency or with an uncontrolled asthma.
• Child who could not discontinue oral or I.V. antihistamines or oral or I.V. corticosteroids at least the week prior to Visit 1.
• Child with important skin lesions precluding the application of the disks.
• Child not affiliated to social security.

• Minimum Eligible Age: 5 Years
• Maximum Eligible Age: 17 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

DBV Technologies

INDUSTRY

Sponsor Role: collaborator

Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Christophe Dupont, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Assistance Publique - Hôpitaux de Paris

Locations

Hopital Necker

Paris, , France

Countries

France

Other Identifiers

2010-019541-26

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

A100293-36

Identifier Type: OTHER

Identifier Source: secondary_id

P091102

Identifier Type: -

Identifier Source: org_study_id