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Efficacy and Safety of XG-102 in Reduction of Post-cataract Surgery Intraocular Inflammation

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT02235272
Recruitment Status : Completed
First Posted : September 9, 2014
Last Update Posted : January 24, 2017
Information provided by (Responsible Party):
Xigen SA

Brief Summary:
The purpose of this study is to evaluate the clinical efficacy and safety of XG-102 (900µg) compared to vehicle in the treatment of subjects with inflammation and pain following cataract surgery.

Condition or disease Intervention/treatment Phase
Inflammation Pain Cataract Drug: XG-102 Drug: Placebo Phase 3

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 339 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: A Multicenter, Randomized, Double-masked, Vehicle-controlled, Parallel Group Phase III Study of the Efficacy and Safety of a Single Sub-conjunctival Injection of XG-102 for the Reduction of Post-cataract Surgery Intraocular Inflammation
Study Start Date : September 2014
Actual Primary Completion Date : December 2015
Actual Study Completion Date : December 2015

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Cataract

Arm Intervention/treatment
Experimental: XG-102 Drug: XG-102
Comparison of XG-102 versus placebo sub-conjunctival injection efficacy

Placebo Comparator: Placebo Drug: Placebo
comparison of XG-102 versus placebo sub-conjunctival injection efficacy

Primary Outcome Measures :
  1. Absence of anterior chamber cells for the 900µg XG-102 sub-conjunctival injection compared to vehicle [ Time Frame: Day 15 ]
  2. Absence of pain for the 900µg XG-102 compared to vehicle [ Time Frame: Day2 ]

Secondary Outcome Measures :
  1. Use of rescue medication [ Time Frame: up to Day 85 ]

Other Outcome Measures:
  1. Specular microscopy [ Time Frame: Day 85 ]
  2. Adverse event (AE) monitoring [ Time Frame: up to Day 85 ]

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Key Inclusion Criteria:

  • Have provided written informed consent, approved by the appropriate institutional review board;
  • Be greater than or equal to 18 years of age of either sex or any race;
  • Be planning to undergo unilateral cataract extraction via phacoemulsification and posterior chamber intraocular lens (PCIOL) implantation in the study eye;
  • Have a pin-hole visual acuity (VA) < 1.0 logarithm of the minimum angle of resolution (logMAR) in the operative eye and fellow eye as measured using an Early Treatment for Diabetic Retinopathy Study (ETDRS) chart at Visit 1;
  • (For females of childbearing potential) agree to have urine pregnancy testing performed at Visit 1 (must be negative) and at exit visit; must not be lactating; and must agree to use a medically acceptable form of birth control1 throughout the study duration. Women of childbearing potential include all females who have experienced menarche and have not experienced menopause (as defined by amenorrhea for greater than 12 consecutive months) or have not undergone successful surgical sterilization (hysterectomy, bilateral tubal ligation, or bilateral oophorectomy).

Key Exclusion Criteria:

  • Have a known sensitivity or allergy to the class of medication of the active ingredient in the study medication or any of the study medication's components;
  • Have any intraocular inflammation (e.g., white blood cells or flare) present in the study eye at the Visit 1slit lamp examination;
  • Have a score greater than "0" on the Ocular Pain Assessment at Visit 1 or 2 in the study eye;
  • Have an immunosuppressive or an autoimmune disease that in the opinion of the Investigator could affect intraocular inflammation or the normal healing process of the eye;
  • Have active or chronic/recurrent ocular or systemic disease that is uncontrolled and will likely affect wound healing;
  • Currently have suspected or known malignancy or be currently receiving antineoplastic therapy;
  • Be a female who is currently pregnant, planning a pregnancy, lactating, not using a medically acceptable form of birth control throughout the study duration, or have a positive urine pregnancy test at Visit 1;
  • Use anti-inflammatory agents, analgesics/pain relievers (including opioids, narcotics and other pain medications) or immunomodulating agents, systemically, or in either eye, and/or use medications for benign prostatic hyperplasia (BPH), from the washout period through the duration of the study

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT02235272

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United States, California
Garden Grove, California, United States, 92843
Sponsors and Collaborators
Xigen SA
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Principal Investigator: Steven M Silverstein, MD Silverstein Eye Centers
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Responsible Party: Xigen SA Identifier: NCT02235272    
Other Study ID Numbers: SDD-1002-064
First Posted: September 9, 2014    Key Record Dates
Last Update Posted: January 24, 2017
Last Verified: January 2017
Additional relevant MeSH terms:
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Pathologic Processes
Lens Diseases
Eye Diseases
Uveal Diseases