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Completed Phase 3 Interventional Results available

Evaluation of the Efficacy and Safety of OC-01 Nasal Spray on Signs and Symptoms of Dry Eye Disease

ClinicalTrials.gov ID: NCT04036292

Public ClinicalTrials.gov record NCT04036292. 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, 4:40 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

Multicenter, Randomized, Controlled, Double-Masked, Clinical Trial to Evaluate the Efficacy and Safety of OC-01 (Varenicline) Nasal Spray on Signs and Symptoms of Dry Eye Disease (The ONSET-2 Study)

Brief summary

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

The objective of this study is to evaluate the safety and effectiveness of OC-01 Nasal Spray as compared to placebo on signs and symptoms of dry eye disease.

Study identification

NCT ID
NCT04036292
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Oyster Point Pharma, Inc.
Industry
Enrollment
758 participants

Conditions and interventions

Eligibility (public fields only)

Age range
22 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 22, 2019
Primary completion
Apr 9, 2020
Completion
Feb 4, 2021
Last update posted
Nov 21, 2021

2019 – 2021

United States locations

U.S. sites
22
U.S. states
18
U.S. cities
21
Facility City State ZIP Site status
Phoenix Phoenix Arizona 85032
New Port Beach Newport Beach California 92663
Fort Collins Fort Collins Colorado 80528
Waterbury Waterbury Connecticut 06708
Delray Beach Delray Beach Florida 33484
Indianapolis Indianapolis Indiana 46290
Louisville Louisville Kentucky 40206
Raynham Raynham Massachusetts 02767
Las Vegas Las Vegas Nevada 89052
Raleigh Raleigh North Carolina 27603
Shelby Shelby North Carolina 28150
Fargo Fargo North Dakota 58103
Cranberry Township Cranberry Township Pennsylvania 16066
Warwick Warwick Rhode Island 02842
Sioux Falls Sioux Falls South Dakota 57108
Nashville Nashville Tennessee 37210
Austin Austin Texas 78731
Houston Houston Texas 77025
San Antonio San Antonio Texas 78209
San Antonio San Antonio Texas 78229
Layton Layton Utah 84041
Lynchburg Lynchburg Virginia 24502

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 NCT04036292, 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 Nov 21, 2021 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04036292 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →