Trial of Kuvan in Lesch-Nyhan Disease

Behavioral Manifestations of Lesch-Nyhan Disease Clinical Trial

Official title:

Trial of Kuvan™ (Sapropterin) Treatment in Patients With Lesch Nyhan Disease

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT00935753
• Other study ID #: WLN01
• Status: Withdrawn
• Phase: Phase 2/Phase 3
• Start date: April 2009
• Est. completion date: February 2010

Study information

• Verified date: July 2019
• Source: University of California, San Diego
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To assess the possibility that treatment with Kuvan (a form of tetrahydrobiopterin) will lessen the abnormal behavior and/or neurology commonly found in Lesch-Nyhan disease (LND); to assess biochemical changes as measured in blood and urine.

Description:

Lesch-Nyhan disease (LND) is an X-linked disorder of purine metabolism which results from mutation in the gene for the enzyme hypoxanthineguanine phosphoribosyltransferase (HPRT); patients have hyperuricemia, gout, urinary tract calculi, and nephropathy which are effectively treated with allopurinol. There is also a syndrome of dystonia, chorea and athetosis, as well as involuntary self mutilative biting and aggression toward their caretakers, for which there is no treatment.

Kuvan™ is a form of tetrahydrobiopterin (BH4), and is approved to help lower the blood levels of phenylalanine in people who have phenylketonuria (PKU). LND patients have been found to have decreased BH4 in the spinal fluid and brain; BH4 is a precursor of dopamine, which has an effect on behavior. In an earlier study Dr Nyhan found that treatment of LND with 5-hydroxytryptophan and carbidopa abolished the self-injurious behavior but was uniformly transient.

This is a single site open-label protocol for eight subjects age 4 years and older with Lesch-Nyhan Disease documented by deficiency of HPRT.

The study involves three study visits to San Diego and one study visit done locally. The first visit will last 13 days, the following visits are single day visits at week 4 and week 8, and the local study visit is a brief outpatient visit at week 6. Physical and neurological exams, videotaping of the patient's interactions with the study staff, and blood and urine collection for laboratory analyses will be performed at each San Diego visit. A family member or caregiver will be asked to complete a short assessment form and report any illness or medication changes. In addition, the study staff will have weekly telephone contact with the family to discuss any behavioral changes or study drug issues.

If the patient's self injurious behavior becomes worse after starting Kuvan the drug will be discontinued and the patient will be followed until the behavior returns to baseline.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: February 2010
• Est. primary completion date: February 2010
• Accepts healthy volunteers: No
• Gender: All
• Age group: 4 Years and older

Eligibility

Inclusion Criteria:

1. Ages 4 years and older

2. Must have documented evidence of HPRT deficiency.

3. Be on a stable treatment regimen for 30 days or more

4. Willing and able to travel to San Diego for the study visits

5. Have a local neurologist or physician familiar with the patient or experienced in managing behavioral/neuromuscular disorders and willing to assist with study procedures and adverse events if necessary

Exclusion Criteria:

1. Concurrent enrollment in an investigational drug study

2. Currently taking levodopa

3. Elevated liver enzymes

4. Renal or liver impairment or disease

5. Inability to comply with required study procedures

Related Conditions & MeSH terms

• Behavioral Manifestations of Lesch-Nyhan Disease
• Lesch-Nyhan Syndrome

Intervention

Drug:
• sapropterin
oral 100mg tablets taken intact or dissolved in water or apple juice with morning meal for up to 60 days

Locations

Country	Name	City	State
United States	UCSD Mitochondrial and Metabolic Disease Center	San Diego	California

Sponsors (2)

Lead Sponsor	Collaborator
University of California, San Diego	BioMarin Pharmaceutical

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical responses to be monitored will include frequency and severity of self mutilation episodes, frequency and severity of aggressive acts towards others, and any effect on involuntary movements.		Periodically during the eight weeks of treatment per patient
Secondary	Effect of Kuvan on standard chemistries, plasma amino acids, and plasma and urinary catecholamines		Assessed periodically during treatment