Phenylalanine Hydroxylase Deficiencies Clinical Trial
Official title:
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
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.
| Status | Terminated |
| Enrollment | 50 |
| Est. completion date | |
| Est. primary completion date | |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | N/A to 18 Years |
| Eligibility |
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 |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Orphanetics Pharma Entwicklungs GmbH |
Muntau AC, Röschinger W, Habich M, Demmelmair H, Hoffmann B, Sommerhoff CP, Roscher AA. Tetrahydrobiopterin as an alternative treatment for mild phenylketonuria. N Engl J Med. 2002 Dec 26;347(26):2122-32. — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | dietary phenylalanine tolerance | |||
| Primary | safety |