A Study of ASP4070 to Confirm Safety and Immunological Response in Patients With Pollen Allergy

NCT02469688 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 66

Last updated 2024-10-31

No results posted yet for this study

Summary

Examine safety and immunological response for ASP4070 when vaccinated in patients with pollen allergy

Conditions

  • Cedar Pollinosis

Interventions

DRUG

ASP4070

intramuscular or intradermal

DRUG

Placebo

intramuscular or intradermal

Sponsors & Collaborators

  • Immunomic Therapeutics, Inc.

    collaborator INDUSTRY
  • Astellas Pharma Inc

    lead INDUSTRY

Principal Investigators

  • Medical Director · Astellas Pharma Inc

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
64 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-18
Primary Completion
2015-11-27
Completion
2016-07-26

Countries

  • Japan

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Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02469688 on ClinicalTrials.gov