Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01274026 · ClinicalTrials.gov registry record

Evaluation of Behavior, Executive Function, Neurotransmitter Function and Genomic Expression Kuvan Nonresponders

A clinical trial, sponsored by Tulane University School of Medicine.

Completed
Registry status
21
Enrollment target

NCT01274026: Completed study, sponsored by Tulane University School of Medicine.

NCT01274026 is a clinical trial that has completed, run by Tulane University School of Medicine. The registered enrollment target is 21 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01274026 has completed, sponsored by Tulane University School of Medicine.

COMPLETED
Registry status
21 participants
Enrollment target

Study Summary

This observational study seeks to establish evidence: 1. that physiologic changes, unrelated to effect on the Phenylalanine Hydroxylase (PAH) enzyme, occur in Phenylketonuria (PKU) patients who are treated with sapropterin (Kuvan®) therapy, 2. that these changes may be caused by enhanced neurotransmitter synthesis in the brain or an upregulation of gene expression (increasing the ability of genes to produce functional enzymes), 3. and that beneficial changes in behavior and cognition, especially executive functioning skills may result. The objective of this study is to correlate any change in behavior and executive function skills of PKU patients who are non-responsive to sapropterin effect on the PAH enzyme, as defined by lowered blood PHE levels, with urine neurotransmitter levels and broad gene expression prior to and after sapropterin administration. Expected outcomes would include evidence of sapropterin effects on upregulation of enzymes other than PAH that control neurotransmitter synthesis, and any resulting correlation with behavioral and cognitive changes. The investigators hope this study will inform further detailed investigations into the biochemical and molecular actions of sapropterin (Kuvan®) that lead to increased understanding of possible treatment effects beyond a lowered blood PHE response.

Primary Outcome

This study seeks to establish evidence that behavioral changes, unrelated to blood phenylalanine levels, occur in PKU patients who are treated with Kuvan therapy, and that beneficial changes in behavior as measured by validated measurement questionnaires may result.

Interventions

  • DRUG sapropterin dihydrochloride

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2011-01
Est. Completion 2013-12

What the finished NCT01274026 record still lists

NCT01274026 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 21 participants, a relatively small participant target.

The record links to 0 conditions, and to 1 intervention - of which sapropterin dihydrochloride is the first listed.

NCT01274026 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01274026 about?

NCT01274026 is a clinical study titled "Evaluation of Behavior, Executive Function, Neurotransmitter Function and Genomic Expression Kuvan Nonresponders". This observational study seeks to establish evidence: 1. that physiologic changes, unrelated to effect on the Phenylalanine Hydroxylase (PAH) enzyme, occur in Phenylketonuria (PKU) patients who are treated with sapropterin (Kuvan®) therapy, 2. that these changes may be caused by enhanced neurotrans...

What is the current status of trial NCT01274026?

This trial is currently completed. The enrollment target is 21 participants. The study started on 2011-01. Estimated completion is 2013-12.

What interventions are being tested in trial NCT01274026?

The interventions under investigation include: sapropterin dihydrochloride (DRUG).

Who is sponsoring clinical trial NCT01274026?

This trial is sponsored by Tulane University School of Medicine, which has 16 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02447874 · 21 participants · Phase 1

    Arginine Therapy for the Treatment of Pain in Children With Sickle Cell Disease

  • NCT03826992 · 21 participants · Phase 1

    Venetoclax Combined With Vyxeos (CPX-351) for Participants With Relapsed or Refractory Acute Leukemia

  • NCT04107077 · 21 participants · Phase 2

    Phase II Study of the Effects of Laparoscopic Hyperthermic Intraperitoneal Chemotherapy (HIPEC) in Patients With Advanced Gastric Cancer

  • NCT04158635 · 21 participants · Phase 1

    Gemcitabine, Nab-Paclitaxel, and Bosentan for the Treatment of Unresectable Pancreatic Cancer

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01274026, the US trial registry maintained by the National Library of Medicine. NCT01274026 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.