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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02998710
Other study ID # CBS-HCY-NHS-01
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 2017
Est. completion date August 2026

Study information

Verified date April 2024
Source Travere Therapeutics, Inc.
Contact Travere Call Center
Phone 1-877-659-5518
Email medinfo@travere.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of the study is to characterize the clinical course of homocystinuria in pediatric and adult patients aged 1 to 65 years under current clinical management practices


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date August 2026
Est. primary completion date April 2026
Accepts healthy volunteers No
Gender All
Age group 1 Year to 65 Years
Eligibility Inclusion Criteria: - Patients who are clinically diagnosed with homocystinuria - Male/female patients aged 1 to 65 years - Patients who consented and/or assented - Patients who are willing and able to comply with all study-related procedures. Exclusion Criteria: - Medically significant postnatal complications or congenital anomalies that are not associated with homocystinuria - Received any experimental therapy for homocystinuria during the 6 months prior to enrollment or expected to receive any such therapy during duration of the study

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Ireland Travere Investigational Site Dublin
Qatar Travere Investigational Site Doha
United Kingdom Travere Investigational Site Salford Manchester
United States Travere Investigational Site Atlanta Georgia
United States Travere Investigational Site (Enrolling 1 to <5 Year-olds Only) Aurora Colorado
United States Travere Investigational Site Boston Massachusetts
United States Travere Investigational Site - Virtual Site Culver City California
United States Travere Investigational Site Indianapolis Indiana
United States Travere Investigational Site (Enrolling 1 to <5 Year-olds Only) Philadelphia Pennsylvania
United States Travere Investigational Site (Enrolling 1 to <5 Year-olds Only) Washington District of Columbia

Sponsors (1)

Lead Sponsor Collaborator
Travere Therapeutics, Inc.

Countries where clinical trial is conducted

United States,  Ireland,  Qatar,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Changes in Met cycle metabolites levels - tHcy Changes in total homocysteine levels in micromoles. The met cycle metabolites levels and change from baseline will be summarized using descriptive statistics at each visit. 6.5 years
Primary Changes in Met cycle metabolites levels - total Cys Changes in total cysteine levels in micromoles. The met cycle metabolites levels and change from baseline will be summarized using descriptive statistics at each visit. 6.5 years
Primary Changes in Met cycle metabolites levels - Met Changes in total methionine levels in micromoles. The met cycle metabolites levels and change from baseline will be summarized using descriptive statistics at each visit. 6.5 years
Primary Changes in Met cycle metabolites levels - Cth Changes in total cystathionine levels in micromoles. The met cycle metabolites levels and change from baseline will be summarized using descriptive statistics at each visit. 6.5 years
Primary Patient Reported Outcome (PRO): Quality of Life in Neurological Disorders [Neuro-QoL] Short forms for four domains (anxiety, depression, social activities, cognition function) by adults version for age 18+ and pediatric version for age 12-17 are used. A summary score will be calculated for each domain by adding up the scores for individual questions. The aggregated score for each domain as a continuous variable, and the change from baseline in the aggregated domain score will be summarized using descriptive statistics at each visit. 6.5 years
Primary Patient Reported Outcome (PRO): Quality of Life by 36-Item Short Form Survey [SF-36] The original responses to all questions are scored on a scale from 0 to 100, with 100 representing the highest level possible. The rescaled scores that address each specific area of functional health status are averaged together, for a final score within each of the 8 domains measured. The average is based on the number of items with non-missing scores. The average score for each domain and the change from baseline will be summarized using descriptive statistics at each visit. 6.5 years
Primary National Institutes of Health (NIH) Toolbox Cognition Battery The NIH Toolbox is a multi-dimensional assessment tool that is used to measure the neurological and behavioral function of a patient over time. Assessments are recorded as 7 individual test scores, 1 total summary score and 2 composite scores. The raw measure scores and age-corrected standard scores and the change from baseline of the scores will be summarized using descriptive statistics at each visit. 6.5 years
Primary EuroQol EQ-5D™ questionnaire to measure health and quality-of-life EQ-5D™ is a standardized questionnaire as judged by the patients. This questionnaire consists of two parts:
Five domains: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension consists of 5 levels of grading: no problem, slight problem, moderate problem, severe problem and extreme problem. For youths, 3 levels of grading: no problem, some problems, and a lot of problems.
Visual analogue scale (VAS) is a vertical scale from 0 (worst) to 100 (best). Descriptive statistics will be provided for the five domains. Descriptive statistics will be provided for VAS and change from baseline at each visit for pooled EQ-5D-Y version and EQ-5D-5L version.
6.5 years
Primary Dual-Energy X-Ray Absorptiometry to measure bone mineral density The z-score, t-score, and bone mineral density and change from baseline will be summarized by the location of X-ray (spine, hip, and total body) at each visit. 6.5 years
Primary Eye assessments to evaluate ocular health: Visual acuity examination will be performed to determine the clarity or sharpness of vision Visual acuity examination will be performed to determine the clarity or sharpness of vision. The results will be summarized using descriptive statistics at each visit. 6.5 years
Primary Eye assessments to evaluate ocular health: Slit lamp eye examination will be performed to look for any diseases or abnormalities in the anterior portion of the eye Slit lamp eye examination will be performed to look for any diseases or abnormalities in the anterior portion of the eye. The results will be summarized using descriptive statistics at each visit. 6.5 years
Secondary Growth and development: World Health Organization (WHO) growth charts will be used to document height in centimeters (cm) for age 1 to 19 years old. Routine methods will be used to document height for all other age groups. The results will be summarized using descriptive statistics at each visit. 6.5 years
Secondary Growth and development: World Health Organization (WHO) growth charts will be used to document Body Mass Index (BMI) in kilograms per meter square for age 1 to 19 years old. Routine methods will be used to document BMI for all other age groups. The results will be summarized using descriptive statistics at each visit. 6.5 years
Secondary Growth and development: World Health Organization (WHO) growth charts will be used to document weight in kilograms (kg) for age 1 to 19 years old. Routine methods will be used to document weight for all other age groups. The results will be summarized using descriptive statistics at each visit. 6.5 years
Secondary Changes in alanine aminotransferase (ALT) The results will be summarized using descriptive statistics at each visit. 6.5 years
Secondary Changes in aspartate aminotransferase (AST) The results will be summarized using descriptive statistics at each visit. 6.5 years
Secondary Changes in alkaline phosphatase (ALP) The results will be summarized using descriptive statistics at each visit. 6.5 years
Secondary Optional homocystynuria genetic testing The optional test will be done once at screening visit