Study of Phenoptin to Increase Phenylalanine Tolerance in Phenylketonuric Children on a Phenylalanine-restricted Diet
Status: | Completed |
---|---|
Conditions: | Endocrine |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | 4 - 12 |
Updated: | 4/21/2016 |
Start Date: | February 2006 |
End Date: | November 2006 |
A Phase 3, Double-blind, Placebo-controlled Study to Evaluate the Safety and Efficacy of Phenoptin to Increase Phenylalanine Tolerance in Phenylketonuric Children on a Phenylalanine-restricted Diet
The primary objective of this trial is to evaluate the ability of Phenoptin to increase
phenylalanine (phe) tolerance in children with phenylketonuria who are following a
phe-restricted diet.
phenylalanine (phe) tolerance in children with phenylketonuria who are following a
phe-restricted diet.
Inclusion Criteria:
- Clinical diagnosis of PKU with hyperphenylalaninemia (HPA) documented by at least one
blood Phe measurement >/=360 umol/L (6 mg/dL)
- Under dietary control with a Phe-restricted diet as evidenced by:· Estimated daily
Phe tolerance =1000 mg/day
- At least 6 months of blood Phe control (mean level of =480 μmol/L) prior to
enrolling in the study
- Aged 4 to 12 years inclusive at screening
- A blood Phe level =480 μmol/L at screening
- Female subjects of childbearing potential (as determined by the principal
investigator) must have a negative blood or urine pregnancy test at entry (prior to
the first dose). Note: All female subjects of childbearing potential and sexually
mature male subjects must be advised to use a medically accepted method of
contraception throughout the study. Female subjects of childbearing potential must be
willing to undergo periodic pregnancy tests during the course of the study
- Willing and able to comply with all study procedures
- Willing to provide written assent (if applicable) and written informed consent by a
parent or legal guardian after the nature of the study has been explained and prior
to any research-related procedures
Exclusion Criteria:
- Any condition that, in the view of the PI, renders the subject at high risk from
treatment compliance and/or completing the study
- Prior history of organ transplantation
- Perceived to be unreliable or unavailable for study participation or have parents or
legal guardians who are perceived to be unreliable or unavailable
- Use of any investigational agent within 30 days prior to screening, or requirement
for any investigational agent or vaccine prior to completion of all scheduled study
assessments
- ALT > 2 times the upper limit of normal (i.e., Grade 1 or higher based on World
Health Organization Toxicity Criteria) at screening
- Concurrent disease or condition that would interfere with study participation or
safety (e.g., seizure disorder, oral steroid-dependent asthma or other condition
requiring oral or parenteral corticosteroid administration, or insulin-dependent
diabetes)
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