Tetrahydrobiopterin Treatment in Children With Idiopathic Cognitive Developmental Disorders

Autism Spectrum Disorder Clinical Trial

Official title:

Biomarkers of Central Nervous System Tetrahydrobiopterin Concentration and Response to Tetrahydrobiopterin Supplementation in Children With Idiopathic Cognitive Developmental Disorders

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01141595
• Other study ID #: HSC-MS-09-0578
• Status: Completed
• Phase: N/A
• First received: June 8, 2010
• Last updated: February 28, 2014
• Start date: July 2010
• Est. completion date: September 2011

Study information

• Verified date: February 2014
• Source: The University of Texas Health Science Center, Houston
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to develop biomarkers for central nervous system BH4 concentration in children with autism so they can be easily screened to determine if they may benefit from BH4 supplementation. Kuvan is a synthetic form of BH4. BH4 is an enzyme cofactor that is essential for several critical metabolic functions.

Description:

SUMMARY

PURPOSE: The purpose of this study is to develop biomarkers for central nervous system BH4 concentration in children with autism so they can be easily screened to determine if they may benefit from BH4 supplementation. Kuvan is a synthetic form of BH4. BH4 is an enzyme cofactor that is essential for several critical metabolic functions.

Procedures: Consented subjects' behavior, particularly irritability, cognitive and language function will be assessed at baseline to make sure that the subject meets the inclusion and exclusion criteria. Parents of subjects will be instructed to give the subjects 20 mg/kg/day of Kuvan® orally dissolved in 4 - 8oz. of water or apple juice with breakfast. Subjects will not be permitted to start any new supplement treatments during the study period but will be allowed to continue previous supplements. Subjects will be permitted to take over the counter medications or other prescription medications for acute illnesses. Evaluation of subjects will include three clinic visits for neuropsychological and clinical testing, completion of study-related questionnaires and telephone follow-up visits.

Course of Study: Subjects will be in the study for up to 16 weeks.

Enrollment: The study will enroll 20 (male and female) subjects, 2-6 years old, with delays in language and/or social development. Vulnerable populations include children. A pediatric risk assessment was completed by Ian Butler, MD with an outcome of minimum risks to subjects.

Recruitment: Subjects will be recruited when their parents present them for care at the University of Texas medically-based autism clinic.

Known Risks: For the study drug Kuvan, there have been rare associations with gastroesophageal reflux and a previous form of this compound was associated with seizures in individuals taking Levodopa concurrently. There is a risk of loss of confidentiality.

Data Safety Monitoring: A DSMB will not be formed for this study. The PI will be responsible for the data and safety of the study.

Informed Consent: A written parental informed consent form has been submitted for review and approval. There is no cost for participation, and no remuneration. Confidentiality will be maintained through the use of unique study codes.

IND#: A request for a pre-IND meeting with the FDA to discuss the possible IND exemption has been submitted.

Funding Source: This study is being funded by BioMarin Pharmaceuticals.

SCIENTIFIC PRE-REVIEW: The Clinical Research Unit Review Board Committee Scientific Advisory Committee (SAC) completed the submission with the outcome of CRU - Approved on12/10/2009.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 10
• Est. completion date: September 2011
• Est. primary completion date: September 2011
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 2 Years to 6 Years

Eligibility

Inclusion Criteria:

1. Children 2 years 0 months to 6 years 11 months of age will be recruited.

2. Delay in language and/or social development with or without delays in gross and/or fine motor development.

3. CSF BH4 level less than or equal to 30 nM/L as determined by lumbar puncture.

4. Adaptive Behavior greater than 50 as determined by the Vineland Adaptive Behavior Scale.

Exclusion Criteria:

1. Epilepsy / Seizure disorder as determined by medical history.

2. Epileptiform discharges without clinical seizures.

3. Metabolic disorder that would be a contraindication to tetrahydrobiopterin treatment.

4. Genetic disorder

5. Therapies that cannot be maintained at a constant level or have not been ongoing for more than 3 months as determined by medical history

6. Prematurity

7. Developmental delay isolated to motor delay.

8. Current gastroesophageal reflux

9. Current or history of liver or kidney disease

10. Severe irritability (as determined by the aberrant behavior checklist)

11. Drugs known to affect folate metabolism (e.g., methotrexate) and their derivatives

12. Patients who are receiving drugs that affect nitric oxide-mediated vasorelaxation (e.g., PDE-5 inhibitors such as sildenafil, vardenafil, or tadalafil)

13. Patients who are receiving levodopa.

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Autism Spectrum Disorder
• Child Development Disorders, Pervasive
• Developmental Disabilities

Intervention

Drug:
• sapropterin dihydrochloride
Patients will be instructed to take 20 mg/kg/day of Kuvan® orally dissolved in 4 - 8oz. of water or apple juice with breakfast.

Locations

Country	Name	City	State
United States	Arkansas Children's Hospital Research Institute	Little Rock	Arkansas

Sponsors (2)

Lead Sponsor	Collaborator
The University of Texas Health Science Center, Houston	BioMarin Pharmaceutical

Country where clinical trial is conducted

United States, 

References & Publications (3)

Frye RE, DeLatorre R, Taylor HB, Slattery J, Melnyk S, Chowdhury N, James SJ. Metabolic effects of sapropterin treatment in autism spectrum disorder: a preliminary study. Transl Psychiatry. 2013 Mar 5;3:e237. doi: 10.1038/tp.2013.14. — View Citation

Frye RE, Huffman LC, Elliott GR. Tetrahydrobiopterin as a novel therapeutic intervention for autism. Neurotherapeutics. 2010 Jul;7(3):241-9. doi: 10.1016/j.nurt.2010.05.004. Review. — View Citation

Frye RE. Central tetrahydrobiopterin concentration in neurodevelopmental disorders. Front Neurosci. 2010 Jul 8;4:52. doi: 10.3389/fnins.2010.00052. eCollection 2010. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Preschool Language Scales	Change in the raw score from baseline of the Preschool Language Scales over the 16 week period. The raw score was measured at baseline, 8 weeks and 16 weeks after starting treatment and the change over the 16 week period from baseline to the end of the study was calculated. There was no imputed data and the analysis was as treated. The raw score ranged from 0 to 130. Higher scores indicate better performance.	16 weeks	No

External Links

•   Manuscript of Study Results