CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 14 enrolled
Drug / intervention
VTS-270drug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01747135
NCT01747135Phase 1Completed

Hydroxypropyl Beta Cyclodextrin for Niemann-Pick Type C1 Disease

Vtesse, LLC, a Mallinckrodt Pharmaceuticals Company·interventional·Posted Dec 11, 2012·Updated Jul 23, 2021

In Brief

A Phase 1 clinical trial evaluating VTS-270 for Niemann-Pick Disease, Type C1. Completed, enrolled 14 participants across 1 site.

Detailed Summary

Background: \- Hydroxypropyl beta cyclodextrin (HPBCD) is being tested for a disease called Niemann-Pick disease type C1 (NPC1). NPC1 is a genetic disorder that results in gradual loss of nervous system function. Cholesterol and other fats have trouble moving out of the brain cells, which makes the cells work poorly and leads to symptoms. There is no treatment currently approved in the US for NPC1. Researchers want to test if it is safe to use HPBCD for NPC1. They want to see if it can help brain cells process cholesterol better. Objectives: \- To test the safety and effectiveness of HPBCD for NPC1. Eligibility: \- Individuals between 2 and 25 years of age who have been diagnosed with NPC1 and who have not already received HPBCD in an attempt to treat NPC1. Design: * Participants will be screened with a physical exam and medical history. They will provide blood and urine samples for screening. They will also have neurological tests, including tests of hearing, speech and movement. * Participants will have a lumbar puncture (also called a spinal tap) every month to deliver the drug to the spinal fluid that surrounds the brain. The length of the trial will be determined by the safety and efficacy information that is obtained. * Treatment will be monitored with frequent blood and urine tests, cerebral spinal fluid tests, hearing and neurological exams.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 1CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedDec 11, 2012
Enrollment StartJan 1, 2013
Primary CompletionMar 1, 2017
TodayJul 2, 2026
Enrollment to primary: 4.2 yearsPosted 13.6 years ago

Interventions

VTS-270drug