Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional

Safety Study of Tivanisiran to Treat Dry Eye

ClinicalTrials.gov ID: NCT05310422

Public ClinicalTrials.gov record NCT05310422. 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 Jul 22, 2026, 10:55 AM EDT

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

Study identification

NCT ID
NCT05310422
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sylentis, S.A.
Industry
Enrollment
301 participants

Conditions and interventions

Interventions

  • Tivanisiran sodium ophthalmic solution Drug
  • Vehicle ophthalmic solution Drug

Drug

Eligibility (public fields only)

Age range
18 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
Mar 23, 2022
Primary completion
Oct 10, 2023
Completion
Oct 10, 2023
Last update posted
Feb 19, 2024

2022 – 2023

United States locations

U.S. sites
25
U.S. states
12
U.S. cities
24
Facility City State ZIP Site status
Sylentis Investigative Site Chandler Arizona 85021
Sylentis Investigative Site Phoenix Arizona 85032
FYDES Investigative Site Glendale California 91204
Sylentis Investigative Site Hemet California 92545
Sylentis Investigative Site Los Angeles California 85032
Sylentis Investigative Site Murrieta California 92562
Sylentis Investigative Site Newport Beach California 92663
FYDES Investigative Site Delray Beach Florida 33484
FYDES Investigative Site Jacksonville Florida 32256
Sylentis Investigative Site Largo Florida 33773
Sylentis Investigative Site Morrow Georgia 30260
Sylentis Investigative Site Fraser Michigan 48026
Sylentis Investigative Site Kansas City Missouri 64111
FYDES Investigative Site St Louis Missouri 63131
Sylentis Investigative Site Washington Missouri 63090
Sylentis Investigative Site Rochester New York 14618
Sylentis Investigative Site Asheville North Carolina 28803
Sylentis Investigative Site Garner North Carolina 27529
Sylentis Investigative Site Cranberry Township Pennsylvania 16066
Sylentis Investigative Site Rapid City South Dakota 57701
Sylentis Investigative Site Memphis Tennessee 38119
Sylentis Investigative Site Austin Texas 78731
FYDES Investigative Site El Paso Texas 79902
Sylentis Investigative Site San Antonio Texas 78215
Sylentis Investigative Site San Antonio Texas 78230

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 NCT05310422, 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 Feb 19, 2024 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05310422 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →