Phase 1 Study of PRX019 in Healthy Adult Volunteers
NCT06699680 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 50
Last updated 2026-05-14
Summary
The purpose of this study is to assess the safety and tolerability of PRX019 in healthy adult participants.
Conditions
- Healthy Participants Study
Interventions
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
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