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RECRUITING
NCT07280156
PHASE2

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

View on ClinicalTrials.gov

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

BIOLOGICAL

PRX-115

intravenous (IV) infusion

DRUG

Methotrexate (MTX)

Oral MTX 15 mg weekly

OTHER

PRX-115 placebo

intravenous (IV) infusion

OTHER

Placebo-Methotrexate

Oral Placebo-MTX weekly

Locations (1)

Bioclinical Research Alliance, Inc

Miami, Florida, United States