CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 704 enrolled
Drug / intervention
Mometasone furoate nasal spray (MFNS) +3 moredrug
Likely dose
Mometasone furoate nasal spray (MFNS) 200 µgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03855228
NCT03855228Phase 3Completed

Safety and Efficacy of Mometasone Furoate Nasal Spray With the Addition of Loratadine Versus Placebo in the Treatment of Seasonal Allergic Rhinitis (Study No. C94-145)

Organon and Co·interventional·Posted Feb 26, 2019·Updated Feb 9, 2022

In Brief

A Phase 3 clinical trial evaluating Mometasone furoate nasal spray (MFNS), Loratadine, and 2 other interventions for Rhinitis, Allergic. Completed, enrolled 704 participants.

Detailed Summary

The purpose of this study is to evaluate the safety and efficacy of mometasone furoate nasal spray (MFNS) with the addition of loratadine vs MFNS alone, loratadine alone, or placebo, in the treatment of patients with seasonal allergic rhinitis.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--
Collaborators--

Timeline

Phase 3CompletedFinished
199519961997199819992000200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedFeb 26, 2019
Enrollment StartMar 1, 1995
Primary CompletionAug 7, 1995
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 7.4 years ago

Interventions

Mometasone furoate nasal spray (MFNS)drug

Daily dose of 200 µg of mometasone furoate administered as a nasal spray for 15 days.

Loratadinedrug

Daily dose of 10 mg of loratadine administered as an oral tablet for 15 days.

Placebo nasal spraydrug

Daily dose of placebo administered as a nasal spray for 15 days.

Placebo tabletdrug

Daily dose of placebo administered as an oral tablet for 15 days.