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Completed Phase 3 Interventional Results available

Study to Assess the Efficacy of Anti-Bet v 1 Monoclonal Antibodies in Adults to Reduce Symptoms of Seasonal Allergic Rhinitis

ClinicalTrials.gov ID: NCT04709575

Public ClinicalTrials.gov record NCT04709575. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 1:45 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3 Randomized, Double-Blind, Placebo-Controlled Study Assessing the Efficacy of Anti-Bet v 1 Monoclonal Antibodies to Reduce Symptoms of Seasonal Allergic Rhinitis

Study identification

NCT ID
NCT04709575
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Regeneron Pharmaceuticals
Industry
Enrollment
353 participants

Conditions and interventions

Interventions

  • REGN5713 Drug
  • REGN5714 Drug
  • REGN5715 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 13, 2021
Primary completion
Aug 23, 2021
Completion
Aug 23, 2021
Last update posted
Oct 26, 2022

2021

United States locations

U.S. sites
14
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
Regeneron Study Site Bangor Maine 04401
Regeneron Study Site Baltimore Maryland 21224
Regeneron Study Site Plymouth Minnesota 55441
Regeneron Study Site Columbia Missouri 65212
Regeneron Study Site St Louis Missouri 63141
Regeneron Study Site Missoula Montana 59808
Regeneron Study Site Verona New Jersey 07044
Regeneron Study Site Great Neck New York 11021
Regeneron Study Site Cincinnati Ohio 45231
Regeneron Study Site Toledo Ohio 43617
Regeneron Study Site Portland Oregon 97202
Regeneron Study Site Pittsburgh Pennsylvania 15241
Regeneron Study Site Lincoln Rhode Island 02865
Regeneron Study Site Greenfield Wisconsin 53228

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 23 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04709575, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 26, 2022 · Synced Jul 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04709575 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →