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ACTIVE NOT RECRUITING
NCT03570931
PHASE2/PHASE3

A Study to Assess Efficacy and Safety of RT001 in Subjects With Infantile Neuroaxonal Dystrophy

Sponsor: Biojiva LLC

View on ClinicalTrials.gov

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

Interventions

DRUG

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