Status:
TERMINATED
Study to Evaluate the Efficacy and Safety of Filgotinib in Participants With Active Psoriatic Arthritis Who Have an Inadequate Response or Are Intolerant to Biologic DMARD Therapy
Lead Sponsor:
Gilead Sciences
Collaborating Sponsors:
Galapagos NV
Conditions:
Psoriatic Arthritis
Eligibility:
All Genders
18-75 years
Phase:
PHASE3
Brief Summary
The primary objective of this study is to evaluate the effect of filgotinib compared to placebo as assessed by the American College of Rheumatology 20% improvement (ACR20) response in participants wit...
Eligibility Criteria
Inclusion
- Key
- Male or female participants who are 18-75 years of age (19-75 years of age at sites in Republic of Korea, 20-75 years of age at sites in Japan and Taiwan), on the day of signing initial informed consent
- Meet Classification Criteria for Psoriatic Arthritis (CASPAR)
- Have a history consistent with Psoriatic Arthritis (PsA) ≥ 6 months at Screening
- Have active PsA defined as ≥ 3 swollen joints (from a 66 swollen joint count \[SJC\]) and ≥ 3 tender joints (from a 68 tender joint count \[TJC\]) at Screening and Day 1; these may or may not be the same joints at Screening and Day 1
- Must have a documented history or active signs of at least one of the following at Screening
- Plaque psoriasis
- Nail changes attributed to psoriasis
- Have had inadequate response (lack of efficacy after ≥ 12 week duration of therapy) or intolerance to at least one and not more than 3 biologic DMARDs (bioDMARD) administered for the treatment of PsA or psoriasis, as per local guidelines / standard of care
- Prior to the first dose of study drug on Day 1, treatment with bioDMARD(s) should have been discontinued
- Key
Exclusion
- Prior exposure to a janus kinase (JAK) inhibitor \> 2 doses
- Any active / recent infection
- Any chronic and / or uncontrolled medical condition that would put the individual at increased risk during study participation or circumstances which may make a individual unlikely or unable to complete or comply with study procedures and requirements, per investigator judgement
- Any moderately to severely active musculoskeletal or skin disorder other than PsA or plaque psoriasis that would interfere with assessment of study parameters, as per judgement of investigator
- NOTE: Prior history of reactive arthritis or axial spondyloarthritis is permitted if there is documentation of change in diagnosis to PsA or additional diagnosis of PsA
- Any history of an inflammatory arthropathy with onset before age of 16 years old
- Active autoimmune disease that would interfere with assessment of study parameters or increase risk to the individual by participating in the study, (e.g. uveitis, inflammatory bowel disease, uncontrolled thyroiditis, systemic vasculitis, transverse myelitis), per judgement of investigator
- Pregnancy or nursing females
- Active drug or alcohol abuse, as per judgement of investigator
- Note: Other protocol defined Inclusion/Exclusion criteria may apply.
Key Trial Info
Start Date :
November 13 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 18 2021
Estimated Enrollment :
106 Patients enrolled
Trial Details
Trial ID
NCT04115839
Start Date
November 13 2019
End Date
March 18 2021
Last Update
March 18 2022
Active Locations (59)
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1
Medvin Clinical Research
Covina, California, United States, 91723
2
Omega Research Debary, LLC
DeBary, Florida, United States, 32713
3
San Marcus Research Clinic, Inc.
Miami, Florida, United States, 33015
4
Arthritis Center, Inc.
Palm Harbor, Florida, United States, 85234