Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED 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

NCT02851277 · View on ClinicalTrials.gov ↗

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

172 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02851277

The ClinicalTrials.gov registry entry for NCT02851277 describes a study currently listed as completed. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Astellas Pharma Global Development, which has 172 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02851277 reports 8 study locations spanning 8 distinct geographic areas — top geographies include Arkansas, California, Maryland. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

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). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02851277?

This trial is sponsored by Astellas Pharma Global Development, which has 172 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

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