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A Study to Assess Efficacy and Safety of RT001 in Subjects With Infantile Neuroaxonal Dystrophy
Sponsor: Biojiva LLC
Summary
The purpose of this study is to evaluate the efficacy and safety of RT001 in patients with Infantile Neuroaxonal Dystrophy (INAD).
Official title: A Prospective Open-label Study to Assess Efficacy and Safety of RT001 in Subjects With Infantile Neuroaxonal Dystrophy
Key Details
Gender
All
Age Range
18 Months - 10 Years
Study Type
INTERVENTIONAL
Enrollment
19
Start Date
2018-11-05
Completion Date
2022-06-30
Last Updated
2021-10-14
Healthy Volunteers
No
Conditions
Interventions
RT001
RT001 is encapsulated di-deutero synthetic homologue of linoleic acid ethyl ester. Each capsule contains 960 mg of RT001.
Locations (2)
University of California San Francisco, Benioff Children's Hospital
San Francisco, California, United States
Jacobs Levy Genomics and Research Program
Morristown, New Jersey, United States