Long-Term Tetrahydrobiopterin Treatment in PKU Patients of 0-18 Years - Study on Phenylalanine Tolerance and Safety

Double-Blind, Placebo Controlled, Multicentre Study With an Open Label Extension to Evaluate the Efficacy and Safety of Tetrahydrobiopterin (BH4) in Children and Adolescents With Hyperphenylalaninemia Caused by Phenylalanine Hydroxylase Deficiency

Status

Terminated

Phases

Phase 2Phase 3

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00432822

Enrollment

Registered

2007-02-08

Start date

Unknown

Completion date

Unknown

Last updated

2007-09-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Phenylalanine Hydroxylase Deficiencies

Keywords

phenylketonuria, phenylalanine hydroxylase deficiency, BH4, responsive, tetrahydrobiopterin, newborns, infants, children, adolescents

Brief summary

The aim of the study is to confirm the efficacy and safety of BH4 in the treatment of hyperphenylalaninemia caused by phenylalanine hydroxylase deficiency in patients responsive to BH4. The primary objective is to assess the effect of BH4 on phenylalanine tolerance compared to placebo under optimal blood phenylalanine control and to demonstrate safety in 12 months long-term treatment. Additionally population PK will be assessed.

Interventions

DRUGtetrahydrobiopterin (BH4)

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

DOUBLE

Eligibility

Sex/Gender

ALL

Age

No minimum to 18 Years

Healthy volunteers

Inclusion criteria

* Female and male patients, aged 0-18 years * Phenylalanine-4-hydroxylase (PAH) deficiency shown by mutation analysis * Blood phenylalanine concentration in the target range under dietary treatment * Written consent of a parent or legal representative * Assumed availability within the period of study participation * Patients/parents willing and able to follow the recommended diet * Use of an effective method of contraception in female patients of child bearing potential

Exclusion criteria

* BH4-deficiency due to genetic disorders in biosynthesis or recycling of BH4 * History or current evidence of poor diet compliance * History or current evidence of clinically relevant allergic or idiosyncratic reactions to drugs or food * History of allergic reactions to BH4 or its excipients * Positive pregnancy test (ß-HCG in serum) and lactating females * Participation in other drug trials within the last 30 days before start for the study

Design outcomes

Primary

Measure	Time frame
dietary phenylalanine tolerance	—
safety	—

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026