RecruitingPhase 1Phase 2NCT05757141

An Open-Label Exploratory Study of Fosigotifator in Participants With Vanishing White Matter Disease

A Phase 1b/2 Open-label Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Exploratory Efficacy Following Fosigotifator Administration in Adult and Pediatric Subjects With Vanishing White Matter Disease


Sponsor

Calico Life Sciences LLC

Enrollment

50 participants

Start Date

Mar 13, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

Fosigotifator is an investigational drug being researched for the treatment of Vanishing White Matter disease in adult, pediatric and infant participants. This is a 201-week, open-label, multiple cohort study enrolling adults, pediatric and infant participants with Vanishing White Matter disease. Participants will attend regular visits during the course of the study and complete medical assessments, blood tests, questionnaires, and be evaluated for side effects.


Eligibility

Min Age: 6 Months

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Fosigotifator for people with vanishing white matter disease. The study is currently recruiting participants at 5 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGFosigotifator

Oral Use


Locations(5)

Massachusetts General Hospital /ID# 270960

Boston, Massachusetts, United States

Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, United States

University of Utah /ID# 255624

Salt Lake City, Utah, United States

McGill University Health Centre - Glen Site

Montreal, Quebec, Canada

Amsterdam UMC, locatie VUmc /ID# 270955

Amsterdam, North Holland, Netherlands

View Full Details on ClinicalTrials.gov

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NCT05757141


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