A Study of MZE782 in Adults With PKU

NCT07694440 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 38

Last updated 2026-08-20

No results posted yet for this study

Summary

The purpose of this study is to evaluate the safety, tolerability, and efficacy of MZE782 in adults with Phenylketonuria (PKU).

Conditions

  • Phenylketonuria (PKU)

Interventions

DRUG

MZE782

Tablet, Low Dose

OTHER

Placebo

Tablet

DRUG

MZE782

Tablet, High Dose

Sponsors & Collaborators

  • Maze Therapeutics

    lead INDUSTRY

Principal Investigators

  • Medical Director · Maze Therapeutics

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-06-23
Primary Completion
2027-12-31
Completion
2028-02-29
FDA Drug
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07694440 on ClinicalTrials.gov