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NCT02851277 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate Safety, Tolerability and Immune Response in Adults Allergic to Peanut After Receiving Intradermal or Intramuscular Administration of ASP0892 (ARA-LAMP-vax), a Single Multivalent Peanut (Ara h1, h2, h3) Lysosomal Associated Membrane Protein DNA Plasmid Vaccine

A Phase 1 study of Peanut Allergy, sponsored by Astellas Pharma Global Development.

Completed
Registry status
Phase 1
Development phase
31
Enrollment target
8
Study locations

NCT02851277 is a Phase 1 study of Peanut Allergy that has completed, run by Astellas Pharma Global Development. The registered enrollment target is 31 participants, below the 212-participant average among 13 other Peanut Allergy trials with a reported enrollment target (85% lower). The trial reports 8 study locations across 8 states.

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The verdict

NCT02851277, a Phase 1 study of Peanut Allergy, has completed, sponsored by Astellas Pharma Global Development.

COMPLETED
Registry status
Phase 1
Development phase
31 participants
Enrollment target
8
Study locations

Study Summary

The purpose of this study is to evaluate the safety and tolerability of ASP0892 after intradermal or intramuscular injection in adults with peanut allergy.

Conditions Studied

Interventions

  • DRUG ASP0892 Intradermal
  • DRUG ASP0892 Intramuscular
  • DRUG Placebo Intradermal
  • DRUG Placebo Intramuscular

Study Locations (8)

Arkansas

  • Site US10014 - Little Rock

California

  • Site US10008 - Mountain View

Maryland

  • Site US10001 - Baltimore

Massachusetts

  • Site US10002 - Boston

New York

  • Site US10004 - New York

North Carolina

  • Site US10003 - Chapel Hill

Ohio

  • Site US10012 - Cincinnati

Washington

  • Site US10006 - Seattle

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2016-12-13
Est. Completion 2018-12-06
Phase Phase 1

Sponsor

Astellas Pharma Global Development

168 total trials

What the Registry Record Tells You About NCT02851277

The ClinicalTrials.gov registry entry for NCT02851277 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 212-participant average among 13 other Peanut Allergy trials with a reported enrollment target (85% lower). The listed sponsor is Astellas Pharma Global Development, which has 168 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Peanut Allergy appearing as the primary indexed condition, and to 4 interventions - of which ASP0892 Intradermal is the first listed.

NCT02851277 reports 8 study locations spanning 8 distinct geographic areas - top geographies include Arkansas, California, Maryland.

Frequently Asked Questions

What is clinical trial NCT02851277 about?

NCT02851277 is a clinical study titled "A Study to Evaluate Safety, Tolerability and Immune Response in Adults Allergic to Peanut After Receiving Intradermal or Intramuscular Administration of ASP0892 (ARA-LAMP-vax), a Single Multivalent Peanut (Ara h1, h2, h3) Lysosomal Associated Membrane Protein DNA Plasmid Vaccine". The purpose of this study is to evaluate the safety and tolerability of ASP0892 after intradermal or intramuscular injection in adults with peanut allergy.

What is the current status of trial NCT02851277?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 31 participants. The study started on 2016-12-13. Estimated completion is 2018-12-06.

What conditions does trial NCT02851277 study?

This clinical trial studies the following conditions: Peanut Allergy.

What interventions are being tested in trial NCT02851277?

The interventions under investigation include: ASP0892 Intradermal (DRUG), ASP0892 Intramuscular (DRUG), Placebo Intradermal (DRUG), Placebo Intramuscular (DRUG).

Who is sponsoring clinical trial NCT02851277?

This trial is sponsored by Astellas Pharma Global Development, which has 168 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02851277 being conducted?

This trial has 8 study locations across Arkansas, California, Maryland, Massachusetts, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.