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Recruiting Phase 2

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)

NCT07280156 · tracked via the Priya Life Science USA tracker
Sponsor
Protalix
Phase
Phase 2
Started
2025-12-22
Last updated
2026-09-29

Condition(s) studied

Gout

Investigational drug(s) / intervention(s)

PRX-115Methotrexate (MTX) →PRX-115 placeboPlacebo-Methotrexate

PRX-115: intravenous (IV) infusion

Methotrexate (MTX): Oral MTX 15 mg weekly

PRX-115 placebo: intravenous (IV) infusion

Placebo-Methotrexate: Oral Placebo-MTX weekly

Study 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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Males or females ≥18 years of age. 2. Weight within the range of 50.0 - 150.0 kg. 3. Gout patients who failed to normalize sUA (\<7 mg/dL) with or without xanthine oxidase inhibitors or uricosuric agent or have contraindications to these drugs. 4. Willing to discontinue any oral ULT 5. Females who are sterile, postmenopausal, or non-pregnant and using birth control methods. Exclusion Criteria: 1. Any condition known to have arthritis as a clinical manifestation. 2. Positive testing for HBV,HCV, or HIV. 3. The patient is a pregnant or lactating female or plans to become pregnant during the study period. 4. Known allergy or sensitivity to the injected proteins, including pegylated products. 5. Prior exposure to any experimental or marketed uricase. 6. Patient treated with a medication known to have an influence on urate metabolism or clearance such as ULTs. 7. History of anaphylaxis, severe allergic reactions, or severe atopy. 8. G6PD deficiency or known catalase deficiency. 9. History of significant hematologic or autoimmune disorders within 5 years of Screening and/or patient is immunocompromised or treated with immunosuppressive medications. 10. Non-compensated CHF or hospitalization for CHF (Stage 3-4 NYHA Functional Class) within 3 months of the Screening Visit, uncontrolled arrhythmia, treatment for acute coronary syndrome (myocardial infarction or unstable angina), or uncontrolled BP (\>160/100 mmHg) at screening and prior to randomization at Week -4 (Visit 1). 11. Current liver disease, as determined by ALT or AST levels above upper limit of normal at Screening Visit. 12. Chronic liver disease. 13. Hemoglobin \<11 g/dL, neutrophil count \<1500 /µl, or platelet count \<100,000 /µl. 14. Known severe pulmonary fibrosis, bronchiectasis or interstitial pneumonitis. 15. eGFR ≤ 40 mL/min/1.73m2 tested at Screening Visit. Kidney transplant or requires dialysis. 16. Known intolerance and/or known contraindication to MTX treatment or MTX treatment considered inappropriate 17. Has uncontrolled type 2 diabetes at Screening with HbA1c ≥8.5%. Patients with type 1 diabetes will be excluded. 18. Has known latent autoimmune diabetes of adult. 19. Immunocompromised state, regardless of etiology. 20. History or treatment of malignancy in the last 5 years, excluding localized, nonmelanoma skin cancers (e.g. basal or squamous cell)

Primary outcome measure(s)

  • Percentage of Serum Uric Acid (sUA) Responders (sUA < 6 mg/dL) During Month 6 — 6 months of treatment
    Proportion of patients who achieve a reduction in sUA to \<6.0 mg/dL for at least 80% of the time during Month 6

Trial sites (35)

FacilityCityRegionStatus
Rezen Clinical Trials Glendale Arizona Recruiting
Applied Research Center of Arkansas Little Rock Arkansas Recruiting
Advanced Research Center, Inc Anaheim California Recruiting
Triwest Research Associates Llc El Cajon California Recruiting
Imax Clinical Trials, LLC La Palma California Recruiting
Kinetic Clinical Research Long Beach California Recruiting
Clinical Research of West Florida, Inc. Clearwater Florida Recruiting
Accel Research Sites - Deland Clinical Research Unit DeLand Florida Recruiting
ICR Sites East Doral Florida Recruiting
Qway Research Hialeah Florida Recruiting
Bioclinical Research Alliance, Inc Miami Florida Recruiting
D&H National Research Centers (North Miami) Miami Florida Recruiting
Well Pharma Medical Research Group Miami Florida Recruiting
Conquest Research - Lake Nona Orlando Florida Recruiting
Combined Research Orlando Phase I-IV Orlando Florida Recruiting
New Horizons Research Palmetto Bay Florida Recruiting
Clinical Research of West Florida, Inc. Tampa Florida Recruiting
Centricity Research - Columbus Georgia Multispecialty Columbus Georgia Recruiting
Revival Research Institute, LLC Dearborn Michigan Recruiting
Quest Research Institute Farmington Hills Michigan Recruiting
Revive Research Institute, Inc Sterling Heights Michigan Recruiting
Altoona Center for Clinical Research Duncansville Pennsylvania Recruiting
Pioneer Research Solutions Inc Houston Texas Recruiting
Mt. Olympus Medical Research, LLC - Sugar Land Sugar Land Texas Recruiting
Velocity Clinical Research Waco Texas Recruiting
Velocity Clinical Research Suffolk Virginia Recruiting
Aleksandre Aladashvili Clinic LLC, Georgia Tbilisi Georgia Recruiting
Tbilisi Heart and Vascular Clinic Ltd , Georgia Tbilisi Georgia Recruiting
Mediclub Georgia Tbilisi Georgia Recruiting
Tbilisi Institute of Medicine, Georgia Tbilisi Georgia Recruiting
Georgian-Dutch Hospital, Georgia Tbilisi Georgia Recruiting
LTD First Medical Center, Georgia Tbilisi Georgia Recruiting
HaEmek MC, Israel Afula Israel Recruiting
Barzilai MC, Israel Ashkelon Israel Recruiting
Meir MC, Israel Kfar Saba Israel Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07280156 on ClinicalTrials.gov ↗ ← All trials in the USA