Clinical Trials in France / NCT07694440
Recruiting
Phase 2
A Study of MZE782 in Adults With PKU
NCT07694440 · tracked via the Priya Life Science France tracker
Condition(s) studied
Phenylketonuria (PKU)
Investigational drug(s) / intervention(s)
MZE782PlaceboMZE782
MZE782: Tablet, Low Dose
Placebo: Tablet
MZE782: Tablet, High Dose
Study summary
The purpose of this study is to evaluate the safety, tolerability, and efficacy of MZE782 in adults with Phenylketonuria (PKU).
Eligibility
Key Inclusion Criteria:
* Males and females 18 to 75 years old
* Confirmed diagnosis of PKU
* Willing and able to keep diet and protein intake consistent during the study
* For some study groups, is willing and able to stop certain PKU medications before starting study treatment
* For some study groups, may need to meet additional blood phenylalanine level or background-treatment requirements
* Meets minimum blood phenylalanine level requirements for study group
Key Exclusion Criteria:
* Is pregnant, breastfeeding, or planning to become pregnant or conceive a child during the study
* Medical conditions or abnormal test results that could make participation unsafe or make it difficult to complete study procedures or interpret study results
* Has recently received another investigational drug
* Is unable to swallow tablets or tolerate oral medication
Other inclusion/exclusion criteria defined in protocol apply.
Primary outcome measure(s)
- Safety and tolerability based on incidence of adverse events (AEs) — Week 0 to Week 17
- For Cohorts 1A and 1B: Absolute change in plasma Phe levels from Baseline to the mean of plasma Phe levels — Baseline and Weeks 2, 3, and 4
Trial sites (9)
| Facility | City | Region | Status |
|---|---|---|---|
| UCSF Benioff Children's Hospital Oakland | Oakland | California | Recruiting |
| Stanford University Clinical and Translational Research Unit | Palo Alto | California | Recruiting |
| Ann and Robert H. Lurie Children's Hospital of Chicago | Chicago | Illinois | Recruiting |
| Indiana University School of Medicine | Indianapolis | Indiana | Recruiting |
| University of Kentucky Medical Center | Lexington | Kentucky | Recruiting |
| Clinic for Special Children | Gordonville | Pennsylvania | Recruiting |
| University of Tennessee Health Science Center Le Bonheur Children's Hospital | Memphis | Tennessee | Recruiting |
| CHRU Hôpitaux de Tours - Hôpital Bretonneau | Tours | France | Recruiting |
| University College Hospital | London | United Kingdom | Recruiting |
More Maze Therapeutics trials in France
Other trials for the same condition
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07694440 on ClinicalTrials.gov ↗ ← All trials in France