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A Study to Investigate the Clinical Effect and the Safety of PRX-115 Infused Intravenously at Different Dosing Regimens, With and Without Methotrexate, Versus Placebo in Adults Gout Patients (RELEASE)
Sponsor: Protalix
Summary
This is a multicenter, randomized, double-blind, placebo-controlled phase II study assessing the efficacy, safety, and dosing regimen selection of multiple IV infusions of PRX-115 over 24 weeks, with or without MTX, versus the respective placebos in adult patients with gout.
Official title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase 2 Study Assessing the Efficacy, Safety, and Dosing Regimen Selection of Multiple Intravenous Infusions of PRX-115 With and Without Methotrexate Versus Placebo in Adult Patients With Gout (RELEASE)
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
150
Start Date
2025-12-22
Completion Date
2028-06
Last Updated
2026-02-25
Healthy Volunteers
No
Conditions
Interventions
PRX-115
intravenous (IV) infusion
Methotrexate (MTX)
Oral MTX 15 mg weekly
PRX-115 placebo
intravenous (IV) infusion
Placebo-Methotrexate
Oral Placebo-MTX weekly
Locations (1)
Bioclinical Research Alliance, Inc
Miami, Florida, United States