Phase 1 Study of PRX019 in Healthy Adult Volunteers

NCT06699680 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2026-05-14

No results posted yet for this study

Summary

The purpose of this study is to assess the safety and tolerability of PRX019 in healthy adult participants.

Conditions

  • Healthy Participants Study

Interventions

DRUG

PRX019

Specified dose on specified days

DRUG

Placebo

Placebo

Sponsors & Collaborators

  • Prothena Biosciences Ltd.

    lead INDUSTRY

Principal Investigators

  • Chad Swanson · Prothena Biosciences

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
SEQUENTIAL

Eligibility

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

Timeline & Regulatory

Start
2024-11-08
Primary Completion
2026-01-16
Completion
2026-01-16
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

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 NCT06699680 on ClinicalTrials.gov