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Completed Phase 3 Interventional Results available

Efficacy and Safety of GSP 301 Nasal Spray in the Treatment of Seasonal Allergic Rhinitis (SAR)

ClinicalTrials.gov ID: NCT02870205

Public ClinicalTrials.gov record NCT02870205. 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 Sep 3, 2026, 1:25 AM 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 Double-Blind, Randomized, Parallel-Group Seasonal Allergic Rhinitis (SAR) Study to Evaluate the Efficacy, Safety and Tolerability of GSP 301 Nasal Spray Compared With Placebo Nasal Spray and Individual Monotherapy Formulations (Olopatadine Hydrochloride Nasal Spray and Mometasone Furoate Nasal Spray) in Adult and Adolescent Subjects (12 Years of Age and Older)

Brief summary

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

Study to evaluate the efficacy, safety and tolerability of GSP 301 NS compared with placebo NS and individual monotherapy formulations for the treatment of Seasonal Allergic Rhinitis (subjects 12 years of age and older)

Study identification

NCT ID
NCT02870205
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Glenmark Specialty S.A.
Industry
Enrollment
1,176 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
Jul 31, 2016
Primary completion
Dec 31, 2016
Completion
Dec 31, 2016
Last update posted
Apr 5, 2018

2016 – 2017

United States locations

U.S. sites
43
U.S. states
18
U.S. cities
36
Facility City State ZIP Site status
Investigational Site 406 Mission Viejo California
Investigational Site 414 Orange California
Investigational Site 435 San Diego California
Investigational Site 420 Centennial Colorado
Investigational Site 444 Colorado Springs Colorado
Investigational Site 428 Aventura Florida
Investigational Site 412 Miami Florida
Investigational Site 436 Bethesda Maryland
Investigational Site 432 South Dartmouth Massachusetts
Investigational Site 426 Minneapolis Minnesota
Investigational Site 403 Plymouth Minnesota
Investigational Site 443 Columbia Missouri
Investigational Site 441 Rolla Missouri
Investigational Site 440 St Louis Missouri
Investigational Site 405 Bellevue Nebraska
Investigational Site 434 Skillman New Jersey
Investigational Site 408 Rochester New York
Investigational Site 418 Rockville Centre New York
Investigational Site 402 High Point North Carolina
Investigational Site 427 Raleigh North Carolina
Investigational Site 419 Cincinnati Ohio
United States 404 Cincinnati Ohio
United States 407 Edmond Oklahoma
Investigational Site 410 Oklahoma City Oklahoma
Investigational Site 424 Tulsa Oklahoma
Investigational Site 411 Pittsburgh Pennsylvania
Investigational Site 416 Spartanburg South Carolina
Investigational Site 415 Austin Texas
Investigational Site 442 Austin Texas
Investigational Site 417 Boerne Texas
Investigational Site 421 Dallas Texas
Investigational Site 430 Dallas Texas
Investigational Site 431 El Paso Texas
Investigational Site 433 Kerrville Texas
Investigational Site 422 New Braunfels Texas
Investigational Site 401 San Antonio Texas
Investigational Site 413 San Antonio Texas
Investigational Site 425 San Antonio Texas
Investigational Site 437 San Antonio Texas
Investigational Site 400 Waco Texas
Investigational Site 409 Waco Texas
Investigational Site 423 Draper Utah
Investigational Site 439 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 NCT02870205, 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 Apr 5, 2018 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02870205 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →