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Efficacy and Safety Study of IBI-10090 in Patients Undergoing Cataract Surgery

NCT01048593 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 6

Last updated 2018-12-04

Study results available
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Summary

This study will test the efficacy and safety of IBI-10090 for the reduction of ocular inflammation after cataract surgery.

Conditions

  • Inflammatory Reaction Due to Ocular Lens Prosthesis

Interventions

DRUG

IBI-10090

Single intraocular injection

Sponsors & Collaborators

  • ICON Bioscience Inc

    lead INDUSTRY

Principal Investigators

  • David Chang, MD · Altos Eye Physicians

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2010-05-31
Completion
2010-06-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01048593 on ClinicalTrials.gov