drugset / Trial / NCT04762498
A Phase 4, Open-label Study of KRYSTEXXA® (Pegloticase) Co-administered With Methotrexate (MTX) in Patients With Uncontrolled Gout (FORWARD OL)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |