drugset / Trial / NCT04762498

A Phase 4, Open-label Study of KRYSTEXXA® (Pegloticase) Co-administered With Methotrexate (MTX) in Patients With Uncontrolled Gout (FORWARD OL)

NCT04762498

Phase 4 Completed 54 enrolled Amgen
Non-randomizedSequentialOpen-labelTreatment

Summary

This trial is to assess efficacy, safety, blood levels and bodily effects of up to 2 dose levels of intravenous (IV) pegloticase (KRYSTEXXA) infusions at every 4 week intervals (Q4 Weeks) for up to 6 months (Day 1 to 24 weeks with an optional 24 - 48 weeks treatment duration) when given in combination with weekly oral doses of methotrexate (MTX). The goal is to identify an appropriate dose to be administered every 4 weeks to be used for future clinical trials for patients with chronic gout that does not adequately respond to conventional therapy.

Timeline

Start
2021-01-26
Primary completion
2023-05-18
Completion
2023-12-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Methotrexate Small molecule 15 mg Oral
Subject Pegloticase Protein / enzyme biologic 16 mg Intravenous
Subject Pegloticase Protein / enzyme biologic 24 mg Intravenous
Subject Pegloticase Protein / enzyme biologic 32 mg Intravenous

Indications