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Examination of structural remission and reduction of drug free of filgotinib in rheumatoid arthritis patients whose MTX alone or MTX combined with biologics are non responsive.

Examination of structural remission and reduction of drug free of filgotinib in rheumatoid arthritis patients whose MTX alone or MTX combined with biologics are non responsive. - Examination of structural remission and reduction of drug free of filgotinib in rheumatoid arthritis patients whose MTX alone or MTX combined with biologics are non responsive.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000043547
Enrollment
100
Registered
2021-03-08
Start date
2021-03-08
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rheumatoid Arthritis

Interventions

60 weeks Oral administration of 200mg filgotinib daily

Sponsors

DeparShinshu University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients who agree with participation of this study 2.Patients who are more than 20-years-old 3.Patients with filg0tinib administerable

Exclusion criteria

Exclusion criteria: 1.Patients with administration contraindication of JAK inhibitor 2.Patients with sensitivity for filgotinib 3.Patients prior to serious infection 4.Patients with active tuberculosis 5.Patients with end-stage renal failure 6.Patients with severe liver function 7.Patients with less than 1000/mm3 of neutrofils 8.Patients with less than 500/mm3 of lymphocytes 9.Patients with less than 8g/dL of hemoglobin 10.Patients with possibilities of pregnancy or feeding

Design outcomes

Primary

MeasureTime frame
1.Less than 0.5 of mTSS at 24 weeks after the start of this study 2.Less than 0.5 of mTSS at 60 weeks after the start of this study 3.Less than 2.6 of DAS28CRP at 24 weeks after the start of this study 4.Less than 2.6 of DAS28CRP at 60 weeks after the start of this study

Countries

Japan

Contacts

Public ContactYukio Nakamura

Shinshu University School of Medicine Department of Orthopaedic Surgery

yxn14@aol.jp0263372659

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026