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Long-term Safety Study of AR101 in Subjects Who Participated in a Prior AR101 Study (ARC008)

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ClinicalTrials.gov Identifier: NCT03292484
Recruitment Status : Enrolling by invitation
First Posted : September 25, 2017
Last Update Posted : September 14, 2018
Sponsor:
Information provided by (Responsible Party):
Aimmune Therapeutics, Inc.

Brief Summary:
The purpose of this study is to assess AR101's safety and tolerability over an extended dosing period.

Condition or disease Intervention/treatment Phase
Peanut Allergy Biological: AR101 Phase 3

Detailed Description:
This study is enrolling participants by invitation only. This is an open-label, international, long-term safety extension study for eligible subjects who have participated in one of the Aimmune AR101 clinical studies.

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 1100 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Multicenter, Open-label, Long-term Safety Study of AR101 Characterized Oral Desensitization Immunotherapy in Subjects Who Participated in a Prior AR101 Study
Actual Study Start Date : October 11, 2017
Estimated Primary Completion Date : December 2020
Estimated Study Completion Date : December 2021

Arm Intervention/treatment
Treatment arm description
Subjects will be assigned to one of three treatment pathways when first enrolled into ARC008, which is dependent on the treatment received (AR101 or placebo) during the parent study and their tolerance of this treatment regimen (e.g., daily or non-daily schedule).
Biological: AR101
AR101




Primary Outcome Measures :
  1. Incidence of adverse events including serious adverse events (Safety and Tolerability) [ Time Frame: 3 years ]
    The frequency of treatment-related adverse events and serious adverse events during the overall study period



Information from the National Library of Medicine

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Ages Eligible for Study:   4 Years to 55 Years   (Child, Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Key Inclusion Criteria:

  • Prior participation in an Aimmune AR101 clinical study or any future clinical study that identifies ARC008 as a follow-on study option in the protocol
  • Written informed consent and/or assent from subjects/guardians as appropriate
  • Use of effective birth control by sexually active female subjects of childbearing potential

Key Exclusion Criteria:

  • Did not complete a minimum of 3 months of AR101 maintenance therapy if the subject was assigned to AR101 in the parent study
  • Early discontinuation from the parent study
  • Currently receiving or received within 5 years prior to Screening any type of peanut or other food allergen immunotherapy, except AR101 or unless specified in the parent study

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03292484


  Show 74 Study Locations
Sponsors and Collaborators
Aimmune Therapeutics, Inc.
Investigators
Study Chair: Ellen Ashley Director, Clinical Operations

Additional Information:
Responsible Party: Aimmune Therapeutics, Inc.
ClinicalTrials.gov Identifier: NCT03292484     History of Changes
Other Study ID Numbers: ARC008
First Posted: September 25, 2017    Key Record Dates
Last Update Posted: September 14, 2018
Last Verified: September 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided

Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No

Keywords provided by Aimmune Therapeutics, Inc.:
AR101
Characterized Peanut Allergen
OIT (oral immunotherapy)
Peanut Allergy
Allergy
Peanut-Allergic Children
Peanut-Allergic Adults
Desensitization
CPNA (Characterized Peanut Allergen)

Additional relevant MeSH terms:
Hypersensitivity
Peanut Hypersensitivity
Immune System Diseases
Food Hypersensitivity
Hypersensitivity, Immediate