A PET Study of ENX-104 in Healthy Volunteers

NCT07253272 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2025-11-28

No results posted yet for this study

Summary

The study is designed to evaluate the D2/D3 receptor occupancy (RO), safety, tolerability, and pharmacokinetics (PK) of ENX-104 in healthy volunteers.

Conditions

  • Healthy Volunteers

Interventions

DRUG

ENX-104

Oral solution

Sponsors & Collaborators

  • Engrail Therapeutics INC

    lead INDUSTRY

Principal Investigators

  • David George Steel, MBChB · Parexel

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
23 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-02-24
Primary Completion
2025-09-02
Completion
2025-09-02

Countries

  • United Kingdom

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 NCT07253272 on ClinicalTrials.gov