SAR 1118 in Human Subjects Undergoing Pars Plana Vitrectomy

The recruitment status of this study is unknown because the information has not been verified recently.
Verified July 2009 by Johns Hopkins University.
Recruitment status was  Recruiting
Sponsor:
Collaborator:
SARcode Bioscience
Information provided by:
Johns Hopkins University
ClinicalTrials.gov Identifier:
NCT00936520
First received: July 9, 2009
Last updated: December 7, 2009
Last verified: July 2009
  Purpose

The purpose of this study is to determine the safety, tolerability, and pharmacokinetics of SAR 1118 within the anterior and posterior chamber of the eye and plasma in subjects undergoing elective vitrectomy when treated with escalating concentrations of the study drug for approximately 1 week.


Condition Intervention Phase
Diabetic Macular Edema
Pars Plana Vitrectomy
Drug: SAR 1118 0.1%
Drug: SAR 1118 1.0%
Drug: SAR 1118 5.0%
Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Subject)
Primary Purpose: Treatment
Official Title: A Phase 1b, Randomized, Uncontrolled, Single-masked, Safety, Tolerability, and Pharmacokinetic Study of Multiple Doses of Three Different Concentrations (0.1%, 1.0%, 5.0%) of SAR 1118 Ophthalmic Solution in Human Subjects Undergoing Elective Pars Plana Vitrectomy (PPV)

Resource links provided by NLM:


Further study details as provided by Johns Hopkins University:

Primary Outcome Measures:
  • Primary outcome variable: frequency of ocular and non-ocular adverse events judged related to administration of SAR 1118 Ophthalmic Solution, or of inability to tolerate the medication. [ Time Frame: 35 days ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Secondary outcome variable: concentrations of SAR 1118 in aqueous and vitreous on the day of vitrectomy. [ Time Frame: day 9 ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 30
Study Start Date: August 2009
Estimated Study Completion Date: September 2010
Estimated Primary Completion Date: August 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Dose 1
SAR 1118 dose 0.1%
Drug: SAR 1118 0.1%
Daily eye drops (twice daily, ~50 uL each drop) approximately 10 to 12 hours apart; morning and in the evening just prior to bedtime) to the study eye only for 8 consecutive days
Experimental: Dose 2
SAR 1118 dose 1.0%
Drug: SAR 1118 1.0%
Daily eye drops (twice daily, ~50 uL each drop) approximately 10 to 12 hours apart; morning and in the evening just prior to bedtime) to the study eye only for 8 consecutive days
Experimental: Dose 3
SAR 1118 dose 5.0%
Drug: SAR 1118 5.0%
Daily eye drops (twice daily, ~50 uL each drop) approximately 10 to 12 hours apart; morning and in the evening just prior to bedtime) to the study eye only for 8 consecutive days

Detailed Description:

SAR 1118 is a potent and selective small molecule lymphocyte function antigen-1 (LFA-1) antagonist and may be therapeutically useful as a novel topical anti-inflammatory agent in a wide variety of ocular inflammatory conditions including diabetic retinopathy and diabetic macular edema. Recent evidence has demonstrated that topically delivered SAR 1118 ophthalmic solution can be detected in the aqueous, vitreous, and retina 4 to 12 hours after dosing at potentially therapeutic levels in animal models. However, the ability for the current sterile ophthalmic formulation of SAR 1118 to penetrate in sufficiently high therapeutic concentrations into the anterior and posterior chamber in humans is unknown.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Human subjects meeting the following criteria will be enrolled:

    • Age ≥18 years
    • BCVA ≤20/40 in the study eye (BCVA measured at 4M ETDRS)
    • Male or female
    • Current non-smoker (last date of smoking should be at least 60 days before study enrollment)
    • Surgically eligible to undergo elective PPV including, but not limited to, epiretinal membrane, vitreomacular traction, macular holes, or retinal detachment. The elective surgery must be able to be scheduled at least 21 days in advance to allow time for screening and for initiation of study drugs.
    • Females must be non-pregnant, non-lactating, surgically sterile for at least 3 months, post-menopausal for at least 1 years with FSH greater than or equal to 40 mIU/mL, or willing to use an approved method of contraception from 35 days prior to first study drug administration. Approved methods of contraception include: a non-hormonal IUD with spermicide, a female condom with spermicide, a diaphragm with spermicide, a cervical cap with spermicide, use of a condom with spermicide by sexual partner or sterile sexual partner.
    • Willing and able to provide written informed consent after the nature of the study has been explained, and prior to any research-related procedures.
    • Willing and able to comply with all study procedures including follow-up instructions

Exclusion Criteria:

  • Individuals not eligible to participate in this study include those who meet any of the following criteria:

    • Vitreous hemorrhage
    • Active retinal detachment
    • Autoimmune disease of the anterior segment or posterior chamber including chronic keratoconjunctivitis sicca, uveitis, iritis/scleritis, blepharitis of either eye
    • Glaucoma requiring topical medications, infectious conjunctivitis, keratitis, or endophthalmitis of either eye
    • Prior vitrectomy or intraocular lens placement, within 90 days of Day 0
    • Previous intravitreal drug delivery administered in the study eye within the following time period of Day 0:

      • Intravitreal steroid given ≤3 months
      • Intravitreal vascular endothelial growth factor inhibitors given ≤2 months
    • Previous participation in any studies of investigational drugs within 1 month preceding Day 0
    • Any concurrent ophthalmic over-the-counter or topical ocular pharmaceutical within 30 days of Day 0 with the exception of saline tear lubricant.
    • History of malignancy, renal insufficiency, or hepatic insufficiency
    • Positive serum pregnancy test
    • Use of any oral, implantable, or injectable contraceptive within 30 days or 5 half-lives of the contraceptive (whichever is longer) prior to first study drug administration; patients must refrain from these types of contraceptives during the treatment period and may resume the use of such contraceptives following the 1-week observation period.
    • Any history of excessive alcohol (as judged by the Investigator) or illicit drug use/abuse
    • Consumption of any alcohol or any illicit drugs within one week of first study drug administration
    • Use of any tobacco or nicotine-containing products within 2 months prior to first study drug administration
    • Any laboratory abnormality considered clinically significant by the Investigators
    • Subjects with a hemoglobin < 12.0 g/dL
    • Any clinically significant acute or chronic medical condition that would preclude participation in a clinical study
    • Any history of autoimmune disease, immunodeficiency disorder, positive HIV, acute hepatitis A (IgM positive), or hepatitis B, or C, or organ or bone marrow transplant
    • Participation in an ongoing investigational drug or medical device study
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00936520

Contacts
Contact: Ovais Shaikh, MD 410-502-3467 oshaikh1@jhmi.edu
Contact: Diana V Do, MD 410-614-3495 ddo@jhmi.edu

Locations
United States, Maryland
Johns Hopkins University Recruiting
Baltimore, Maryland, United States, 21287
Principal Investigator: Diana V Do, MD         
Sub-Investigator: Peter A Campochiaro, MD         
Sub-Investigator: Peter L Gehlbach, MD, PhD         
Sub-Investigator: Gulnar Hafiz, MD         
Sub-Investigator: James T Handa, MD         
Sub-Investigator: Quan D Nguyen, MD, MSc         
Sub-Investigator: Howard C Ying, MD, PhD         
Sub-Investigator: Ingrid Zimmer-Galler, MD         
Sponsors and Collaborators
Johns Hopkins University
SARcode Bioscience
Investigators
Principal Investigator: Diana V Do, MD Johns Hopkins University
  More Information

No publications provided

Responsible Party: Dr. Diana V. Do, MD, Johns Hopkins University
ClinicalTrials.gov Identifier: NCT00936520     History of Changes
Other Study ID Numbers: NA_00029830
Study First Received: July 9, 2009
Last Updated: December 7, 2009
Health Authority: United States: Food and Drug Administration

Keywords provided by Johns Hopkins University:
Diabetic Macular Edema
DME
Pars Plana Vitrectomy
Ocular Inflammation

Additional relevant MeSH terms:
Edema
Macular Edema
Signs and Symptoms
Macular Degeneration
Retinal Degeneration
Retinal Diseases
Eye Diseases
Ophthalmic Solutions
Pharmaceutical Solutions
Therapeutic Uses
Pharmacologic Actions

ClinicalTrials.gov processed this record on August 26, 2014