A Randomized, Double-Blind, Parallel-Group, Placebo Controlled Trial to Assess the Efficacy, Safety, Tolerability, and Pharmacokinetics of Clemastine Fumarate as a Remyelinating Agent in Acute Optic Neuritis

Who is this study for? Patients with Optic Neuritis
What treatments are being studied? Clemastine
Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

The main purpose of this study is to assess clemastine as a remyelinating agent in patients with acute optic neuritis.The study will also evaluate the tolerability of clemastine, originally approved as first-generation antihistamine, in patients with optic neuritis. Study procedures will include assessments for evidence of remyelination in the anterior visual pathway and in the brain using electrophysiologic techniques and magnetic resonance imaging. If they are on one, patients in this study can remain on their standard disease modifying treatment during the course of the study. However, patients cannot participate in any other investigational new drug research study concurrently.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 55
Healthy Volunteers: f
View:

• Patients diagnosed or suspected to have an acute demyelinating optic neuritis in at least one eye within 3 weeks from the onset of any visual symptom other than pain

• Use of disease-modifying therapies is not a contraindication

• Use of appropriate contraception during the period of trial (women)

• Understand and sign the informed consent

Locations
United States
California
University of California San Francisco
RECRUITING
San Francisco
Contact Information
Primary
Harkeerat Halait
Harkeerat.Halait@ucsf.edu
415.353.2707
Backup
Angelica Montevirgen, BS
Angelica.Montevirgen@ucsf.edu
415.745.1304
Time Frame
Start Date: 2017-02-28
Estimated Completion Date: 2026-08
Participants
Target number of participants: 90
Treatments
Experimental: Clemastine
Participants will receive clemastine until 3 months and then will be off treatment until 9 month time point.
Placebo_comparator: Placebo
Participants will receive placebo until 3 months and then will be off treatment until 9 month time point.
Related Therapeutic Areas
Sponsors
Leads: University of California, San Francisco
Collaborators: Moorfields Eye Hospital NHS Foundation Trust

This content was sourced from clinicaltrials.gov

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