Clinical Trials Logo

Clinical Trial Summary

This is a 16-Week Randomized, Double-Blind, Placebo Controlled, Parallel-Group, Multicenter Study Evaluating the Efficacy and Safety of OPN-375 186 μg Twice a Day (BID) in Adolescents with Bilateral Nasal Polyps followed by a 12-Week Open-Label Treatment Phase. The total planned number of subjects is approximately 120 adolescents (12-17 years of age) who will be randomly assigned to receive 1 of 2 study treatments using a 2:1 ratio (OPN-375 186 μg: Placebo). For the PK sub-study, up to 14 subjects will be enrolled to obtain 10 completers.


Clinical Trial Description

The primary objective of this study is to evaluate the efficacy of intranasal administration of OPN-375 186 μg Twice a Day (BID) versus placebo in adolescents with bilateral nasal polyposis and nasal congestion by analyzing the reduction of nasal congestion/obstruction symptoms at the end of Week 4 measured by the 7-day average instantaneous morning diary symptom scores and the reduction in total polyp grade at Week 16 as determined by a nasal polyp grading scale score measured using a 0 to 6 point severity grading scale. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03747458
Study type Interventional
Source Optinose US Inc.
Contact Kim Koob
Phone 215-485-1465
Email kim.koob@optinose.com
Status Recruiting
Phase Phase 3
Start date December 31, 2018
Completion date March 2026

See also
  Status Clinical Trial Phase
Completed NCT01624662 - Efficacy and Safety Study of Intranasal Administration of 100, 200, and 400 μg of Fluticasone Propionate Using a Novel Bi-directional Device Phase 3
Completed NCT03688555 - A Study to Evaluate the Effect of ACT-774312 in Subjects With Bilateral Nasal Polyposis Phase 2
Completed NCT01622569 - Study Evaluating the Efficacy and Safety of Intranasal Administration of 100, 200, and 400 μg of Fluticasone Propionate Twice a Day (BID) Using a Novel Bi Directional Device in Subjects With Bilateral Nasal Polyposis Followed by an 8-Week Open-Label Extension Phase to Assess Safety Phase 3