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Completed Phase 3 Interventional Results available

Safety and Efficacy of KPI-121 in Subjects With Postsurgical Inflammation

ClinicalTrials.gov ID: NCT02163824

Public ClinicalTrials.gov record NCT02163824. 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 Oct 21, 2026, 9:56 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 Phase III, Double-Masked, Randomized, Controlled Trial of KPI-121 in Postsurgical Inflammation

Brief summary

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

The primary purpose of this study is to determine the efficacy and safety of KPI-121 ophthalmic suspension compared to placebo in subjects who have undergone cataract surgery. The efficacy and safety of two different concentrations and two different dosing regimens of KPI-121 are also being assessed.

Study identification

NCT ID
NCT02163824
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Kala Pharmaceuticals, Inc.
Industry
Enrollment
380 participants

Conditions and interventions

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
May 2014 (Type not available)
Primary completion
Dec 2014 (Actual)
Completion
Dec 2014 (Actual)
Last update posted
Jan 29, 2021

2014

United States locations

U.S. sites
23
U.S. states
12
U.S. cities
20
Facility City State ZIP Site status
Sall Research Medical Center Artesia California 90701 —
North Valley Eye Medical Group Mission Hills California 91345 —
Martel Eye Medical Group Rancho Cordova California 95670 —
Wolstan & Goldberg Eye Associates Torrance California 90505 —
Clayton Eye Center Morrow Georgia 30260 —
Price Vision Group Indianapolis Indiana 46260 —
John-Kenyon American Eye Institute New Albany Indiana 47150 —
Taustine Eye Center Louisville Kentucky 40217 —
Tauber Eye Center Kansas City Missouri 64111 —
Tekwani Vision Center St Louis Missouri 63128 —
Ophthalmology Associates St Louis Missouri 63131 —
Ophthalmology Consultants St Louis Missouri 63131 —
Las Vegas Physicians Research Group Henderson Nevada 89052 —
Raymond Fong, MDPC New York New York 10013 —
Rochester Ophthalmological Group, PC Rochester New York 14618 —
Cornerstone Eye Care High Point North Carolina 27262 —
Cincinnati Eye Institute Cincinnati Ohio 45242 —
The Eye Center of Columbus Columbus Ohio 43215 —
Westside Research, LLC Spartanburg South Carolina 29306 —
The Eye Clinic of Texas, Affiliate of Houston Eye Associates League City Texas 77573 —
R&R Eye Research, LLC San Antonio Texas 78229 —
Kozlovsky Delay & Winter Eye Consultants, LLC San Antonio Texas 78230 —
Virginia Eye Consultants Norfolk Virginia 23502 —

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 NCT02163824, 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 Jan 29, 2021 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02163824 live on ClinicalTrials.gov.

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