NAC Attack, A Phase III, Multicenter, Randomized, Parallel, Double Masked, Placebo-Controlled Study Evaluating the Efficacy and Safety of Oral N-Acetylcysteine in Patients With Retinitis Pigmentosa

Status: Active_not_recruiting
Location: See all (31) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

Retinitis pigmentosa (RP) is an inherited retinal degeneration caused by one of several mistakes in the genetic code. Such mistakes are called mutations. The mutations cause degeneration of rod photoreceptors which are responsible for vision in dim illumination resulting in night blindness. After rod photoreceptors are eliminated, gradual degeneration of cone photoreceptors occurs resulting in gradual constriction of side vision that eventually causes tunnel vision. Oxidative stress contributes to cone degeneration. N-acetylcysteine (NAC) reduces oxidative stress and in animal models of RP it slowed cone degeneration. In a phase I clinical trial in patients with RP, NAC taken by month for 6 months caused some small improvements in two different vision tests suggesting that long-term administration of NAC might slow cone degeneration in RP. NAC Attack is a clinical trial being conducted at many institutions in the US, Canada, and Europe designed to determine if taking NAC for several years provides benefit in patients with RP.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

⁃ General

• Ability and willingness to provide informed consent

• Age ≥ 18 and ≤65 years at time of signing Informed Consent Form

• Ability and willingness to comply with the study protocol and to participate in all study visits and assessments in the investigator's judgement

• For candidates of childbearing potential: willingness to use a method of contraception

• Agreement not to take supplements other than vitamin A

⁃ Ocular Inclusion Criteria

• Both eyes must exhibit the RP phenotype with evidence of loss of night vision, gradual constriction of visual fields, and maintenance of visual acuity;

• In addition, an eye must meet the following criteria to be included in the study:

• Gradable EZ on a horizontal SD-OCT scan through the fovea center with width ≤ 8000 µm and ≥1500 µm and with well-defined truncation at both the nasal and temporal sides;

• BCVA ≥ ETDRS letter score of 61 (20/60 Snellen equivalent);

• Sufficiently clear ocular media and adequate pupillary dilation to allow good quality images sufficient for analysis and grading by central reading center.

Locations
United States
California
University of California - Davis, Department of Ophthalmology & Vision Science
Davis
University of Southern California, Keck School of Medicine
Los Angeles
University of California - San Francisco, Department of Ophthalmology
San Francisco
Stanford University, Byers Eye Institute
Stanford
Florida
Vitreo Retinal Associates
Gainesville
University of Florida - Jacksonville, UF Health Jacksonville
Jacksonville
University of Miami, Bascom Palmer Eye Institute
Miami
Georgia
Emory University, Emory Eye Center
Atlanta
Iowa
University of Iowa, Carver College of Medicine
Iowa City
Illinois
University Of Illinois At Chicago
Chicago
Northwestern University
Evanston
Massachusetts
Harvard University, Mass. Eye and Ear
Boston
Maryland
Wilmer Eye Institute- Johns Hopkins University
Baltimore
Michigan
University of Michigan, Kellogg Eye Center
Ann Arbor
Minnesota
University of Minnesota, Department of Ophthalmology and Visual Neurosciences
Minneapolis
Mayo Clinic, Department of Ophthalmology
Rochester
Oklahoma
University of Oklahoma, Dean McGee Eye Institute
Oklahoma City
Pennsylvania
Scheie Eye Institute
Philadelphia
Tennessee
Vanderbilt University, Vanderbilt Eye Institute
Nashville
Texas
Retina Foundation of the Southwest
Dallas
Utah
University of Utah, Moran Eye Center
Salt Lake City
Washington
University of Washington, Department of Ophthalmology
Seattle
Wisconsin
University of Wisconsin - Madison, McPherson Eye Research Institute
Madison
Medical College of Wisconsin, The Eye Institute
Milwaukee
Other Locations
Austria
Medical University of Graz, Department of Ophthalmology
Graz
Canada
McGill University, The Research Institute of the McGill University Health Center
Montreal
Germany
University of Tübingen, Department für Augenheilkunde
Tübingen
Netherlands
University of Amsterdam, Amsterdam Medical Center
Amsterdam
Radboud University, Radboud University Medical Centre
Nijmegen
Switzerland
Universitätsspital Basel, Eye Clinic
Basel
United Kingdom
University College London, Moorfields Eye Hospital
London
Time Frame
Start Date: 2023-10-11
Completion Date: 2029-05
Participants
Target number of participants: 483
Treatments
Experimental: Group 1 - N-acetylcysteine
This is the intervention group. Patients in this group will be receiving 1800 mg of N-acetylcysteine in the form of 3 effervescent 600 mg tablets dissolved in water twice a day for 45 months.
Placebo_comparator: Group 2 - Placebo
Patients in the placebo group will receive identical effervescent tablets lacking active drug.
Sponsors
Collaborators: University of Amsterdam, University of Southern California, University of Florida, Stanford University, University of Miami, Medical College of Wisconsin, University of Michigan, University of Wisconsin, Madison, University of Oklahoma, Duke University, Retina Foundation of the Southwest, University of Minnesota, University of Washington, Northwestern University, University of Iowa, McGill University, University of Utah, University College London Hospitals, Universität Tübingen, University of Houston, Massachusetts Eye and Ear Infirmary, Mayo Clinic, Emory University, Vanderbilt University, Vitreo Retinal Associates, PA, Radboud University Medical Center, University Hospital, Basel, Switzerland, University of Pennsylvania, Medical University of Graz, University of California, Davis, National Eye Institute (NEI)
Leads: Johns Hopkins University

This content was sourced from clinicaltrials.gov