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Completed Phase 3 Interventional Results available

Clinical Equivalence Study of Mometasone Nasal Spray

ClinicalTrials.gov ID: NCT01850823

Public ClinicalTrials.gov record NCT01850823. 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 Oct 23, 2026, 5:40 PM EDT

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A Double-Blind, Randomized, Placebo-Controlled, Parallel Group, Multi-Site Study to Compare the Clinical Equivalence of Mometasone Nasal Spray (Watson Laboratories, Inc) with NASONEX® Nasal Spray (Schering Corporation) in the Relief of the Signs and Symptoms of Seasonal Allergic Rhinitis

Study identification

NCT ID
NCT01850823
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Actavis Inc.
Industry
Enrollment
880 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 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
Feb 2013 (Type not available)
Primary completion
Dec 2013 (Actual)
Completion
Dec 2013 (Actual)
Last update posted
Aug 19, 2020

2013

United States locations

U.S. sites
25
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Investigator site 18 Stockbridge Georgia — —
Investigator site 1 Louisville Kentucky — —
Investigator site 3 Bethesda Maryland — —
Investigator Site 19 Minneapolis Minnesota — —
Investigator Site 24 St Louis Missouri — —
Investigator site 22 Bellevue Nebraska — —
Investigator Site 23 Skillman New Jersey — —
Investigator site 2 Corning New York — —
Investigator site 9 High Point North Carolina — —
Investigator site 20 Raleigh North Carolina — —
Investigator site 25 Cincinnati Ohio — —
Investigator site 21 Sylvania Ohio — —
Investigator site 16 Spartanburg South Carolina — —
Investigator Site 10 Austin Texas — —
Investigator Site 12 Austin Texas — —
Investigator site 6 Austin Texas — —
Investigator Site 11 Kerrville Texas — —
Investigator Site 7 New Braunfels Texas — —
Investigator Site 13 San Antonio Texas — —
Investigator site 14 San Antonio Texas — —
Investigator site 5 San Antonio Texas — —
Investigator site 8 San Antonio Texas — —
Investigator site 4 Waco Texas — —
Investigator Site 15 Draper Utah — —
Investigator Site 17 Greenfield Wisconsin — —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01850823, 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 Aug 19, 2020 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01850823 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →