Rheumatoid Arthritis (RA) Clinical Trial
Official title:
A Nationwide Post-marketing Study on the Safety of Abatacept Treatment in Denmark Using the DANBIO Register
The purpose of this study is to expand on the ongoing post-marketing monitoring of abatacept to include all participants with rheumatoid arthritis (RA) and psoriatic arthritis (PsA) treated with abatacept captured in Danish Database for Biologic Therapies (DANBIO).
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| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
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Phase 1 | |
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Phase 2 | |
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Phase 3 | |
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| Not yet recruiting |
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Vitamin d Level and it's Association With Disease Activity in Egyptian Rheumatoid Arthritis Patients
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| Completed |
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A Study to Investigate the Safety and Efficacy of ABBV-105 Alone or in Combination With Upadacitinib (ABBV-599 Combination) in Participants With Active Rheumatoid Arthritis
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Phase 2 | |
| Active, not recruiting |
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| Active, not recruiting |
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Pharmacokinetics, Safety and Tolerability Study of Single Dose of Abatacept 125mg Administered Subcutaneously
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Phase 1 | |
| Completed |
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Evaluation of Patient Performance Using the Metoject Device for Subcutaneous Injection in Rheumatoid Arthritis (RA)Patient
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Phase 1 | |
| Completed |
NCT04497597 -
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||
| Terminated |
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| Completed |
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Phase 3 | |
| Completed |
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Impact of AbbVie Care Patient Support Program on Clinical, Health Economic and Patient Reported Outcomes, in Crohn's Disease, Ulcerative Colitis, Rheumatoid Arthritis, Psoriatic Arthritis, Psoriasis and Axial Spondyloarthritis, in the Portuguese National Health Service
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| Completed |
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A Phase 3 Study to Compare Upadacitinib to Abatacept in Subjects With Rheumatoid Arthritis on Stable Dose of Conventional Synthetic Disease- Modifying Antirheumatic Drugs (csDMARDs) Who Have an Inadequate Response or Intolerance to Biologic DMARDs
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Phase 3 | |
| Terminated |
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Safety and Efficacy of MK-8457 and Methotrexate (MTX) in Participants With Active Rheumatoid Arthritis Despite MTX Therapy (P08683, MK-8457-008)
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Phase 2 | |
| Completed |
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Phase 1 | |
| Completed |
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Actual Human Use of Methotrexate (MTX) Subcutaneously Administered Via the VIBEX™ MTX Auto-Injector Device
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Phase 2 | |
| Completed |
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Prevalence Study of Gastrointestinal Risk Factors in Patients With Osteoarthritis (OA), Rheumatoid Arthritis (RA) and Ankylosing Spondylitis (AS).
|
N/A | |
| Completed |
NCT01618968 -
Comparison of Methotrexate (MTX) and the VIBEX™ MTX Device
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Phase 2 |