Recruiting
Phase 2

PRX-115 with MTX

Sponsor:

Protalix

Code:

NCT07280156

Conditions

Gout

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

PRX-115

Methotrexate (MTX)

PRX-115 placebo

Placebo-Methotrexate

Study Details

Brief 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.

Conditions

Gout

Study ID

NCT07280156

Start date

Dec 22, 2025

Status verified date

May, 2026

Completion date

Jun, 2028

Anticipated

Primary completion date

Dec, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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)

Study Design

Enrollment

150 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: E4W with placebo-MTX

IV infusion of PRX-115 every 4 weeks (E4W) for a total of 6 doses with placebo-MTX

experimental: E4W with MTX

IV infusion of PRX-115 every 4 weeks (E4W) for a total of 6 doses with MTX

experimental: E6W with MTX

IV infusion of PRX-115 every 6 weeks (E6W) for a total of 4 doses with MTX

experimental: E8W with MTX

IV infusion of PRX-115 every 8 weeks (E8W) for a total of 3 doses with MTX

placebo comparator: placebo E4W

infusion of PRX-115 placebo every 4 weeks (E4W) for a total of 6 doses with placebo-MTX

placebo comparator: placebo E6W

IV infusion of PRX-115 placebo every 6 weeks (E6W) for a total of 4 doses with placebo-MTX

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

Primary outcome measure

  • Percentage of Serum Uric Acid (sUA) Responders (sUA < 6 mg/dL) During Month 6 [ Time Frame: 6 months of treatment ]

Central Contacts and Locations

Central contacts

Head of Clinical Development

+972-4-902-8100info@protalix.com

Locations

Applied Research Center of Arkansas

Recruiting

Little Rock, Arkansas, United States, 72205

Triwest Research Associates Llc

Recruiting

El Cajon, California, United States, 91910

Clinical Research of West Florida, Inc.

Recruiting

Clearwater, Florida, United States, 33765

Accel Research Sites - Deland Clinical Research Unit

Recruiting

DeLand, Florida, United States, 32720

ICR Sites East

Recruiting

Doral, Florida, United States, 33125

Qway Research

Recruiting

Hialeah, Florida, United States, 33010

Bioclinical Research Alliance, Inc

Recruiting

Miami, Florida, United States, 33155

D&H National Research Centers (North Miami)

Recruiting

Miami, Florida, United States, 33169

Well Pharma Medical Research Group

Recruiting

Miami, Florida, United States, 33173

Conquest Research - Lake Nona

Recruiting

Orlando, Florida, United States, 32832

Combined Research Orlando Phase I-IV

Recruiting

Orlando, Florida, United States, 32897

New Horizons Research

Recruiting

Palmetto Bay, Florida, United States, 33176

Clinical Research of West Florida, Inc.

Recruiting

Tampa, Florida, United States, 33606

Centricity Research - Columbus Georgia Multispecialty

Recruiting

Columbus, Georgia, United States, 31904

Quest Research Institute

Recruiting

Farmington Hills, Michigan, United States, 48334

Altoona Center for Clinical Research

Recruiting

Duncansville, Pennsylvania, United States, 16635

Pioneer Research Solutions Inc

Recruiting

Houston, Texas, United States, 77099

Mt. Olympus Medical Research, LLC - Sugar Land

Recruiting

Sugar Land, Texas, United States, 77479

More Information

Sponsor

Protalix

Last update posted

Jun 11, 2026

Last verified

May, 2026

Keywords

  • gout
  • uricase
  • uric acid
  • hyperuricemia
  • PRX-115

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Protalix on 2026-06-11.