Study to Evaluate the Effects of Kuvan on Individuals With Phenylketonuria (PKU) With Maladaptive Behaviors

This study has been completed.
Sponsor:
Collaborator:
BioMarin Pharmaceutical
Information provided by (Responsible Party):
Shoji Yano, University of Southern California
ClinicalTrials.gov Identifier:
NCT00728676
First received: July 30, 2008
Last updated: January 17, 2013
Last verified: January 2013
  Purpose

To validate the outcome measures and the tolerability of Kuvan treatment in the improvement of behavioral symptoms in 10 selected adults with Phenylketonuria (PKU) with or without mental retardation.


Condition
Phenylketonuria

Study Type: Observational
Study Design: Observational Model: Case Control
Time Perspective: Prospective
Official Title: Pilot Study to Evaluate the Effects of Kuvan on Adult Individuals With Phenylketonuria With Measurable Maladaptive Behaviors

Resource links provided by NLM:


Further study details as provided by University of Southern California:

Primary Outcome Measures:
  • Pattern of change from baseline to 6 and 12 months in Vineland scale standard scores, evaluated with a repeated measure ANOVA approach. [ Time Frame: One year ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Correlation and regression methods (non-linear if appropriate) to examine the relationship between changes in behavior and in amino acid profiles. [ Time Frame: one year ] [ Designated as safety issue: No ]

Enrollment: 10
Study Start Date: August 2008
Study Completion Date: May 2010
Primary Completion Date: March 2010 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Individuals with PKU followed at our clinic

Criteria

Inclusion Criteria:

  • Biochemical confirmation of PKU,
  • Measurable maladaptive behavior at baseline,
  • Signed informed consent,
  • Not pregnant or lactating,
  • Females on birth control if applicable,
  • Willing to comply.

Exclusion Criteria:

  • Subjects or care provider unreliable, use of investigational products within 30 days prior to enrollment,
  • Pregnant or lactating,
  • Concurrent disease or condition that would interfere with study participation or safety, ie multiple psychotropic meds, any condition the PI renders the subject at high risk, on drugs that inhibit folate synthesis,
  • Concurrent use of levodopa.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00728676

Locations
United States, California
LAC+USC Medical Center
Los Angeles, California, United States, 90033
Sponsors and Collaborators
Shoji Yano
BioMarin Pharmaceutical
Investigators
Principal Investigator: Shoji Yano, MD, Ph.D. University of Southern California
  More Information

No publications provided

Responsible Party: Shoji Yano, Director, Genetics Division,, University of Southern California
ClinicalTrials.gov Identifier: NCT00728676     History of Changes
Other Study ID Numbers: BioMarin-300
Study First Received: July 30, 2008
Last Updated: January 17, 2013
Health Authority: United States: Institutional Review Board

Keywords provided by University of Southern California:
PKU,
Phe,
PAH,
Kuvan,
Trp,
Tyr

Additional relevant MeSH terms:
Phenylketonurias
Brain Diseases, Metabolic, Inborn
Brain Diseases, Metabolic
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Amino Acid Metabolism, Inborn Errors
Metabolism, Inborn Errors
Genetic Diseases, Inborn
Metabolic Diseases

ClinicalTrials.gov processed this record on August 21, 2014