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The current treatment landscape involves a combination of disease-modifying antirheumatic drugs (DMARDs), biologic agents, and janus kinase (JAK) inhibitors. The goal of treatment is to achieve remission or low disease activity, and to prevent long-term joint damage.","subtype_count":10},"enrichment_level":2,"last_enriched_at":null,"visit_count":0,"created_at":"2026-03-25T12:16:34.963Z","updated_at":"2026-04-19T18:39:44.960Z","meddra_pt":null,"meddra_code":null,"icd10_codes":null,"synonyms":[],"prevalence_global":null,"prevalence_us":null,"marketed_drug_count":111,"pipeline_drug_count":0,"trial_count":0},"drugs":{"marketed":[{"drug_id":"abrilada","indication_name":"Rheumatoid arthritis","indication_type":"approved","phase":null,"line_of_therapy":null,"is_primary_indication":false,"pivotal_trial_result":null,"pivotal_trial_p_value":null,"patient_population":null,"brand_name":"Abrilada","generic_name":"Adalimumab-Afzb","company_name":"AbbVie","drug_phase":"marketed","molecular_target":"Tumor necrosis factor-alpha (TNF-alpha)","drug_class":"TNF blocker","quality_score":10,"revenue":"10191","mechanism":"Adalimumab-afzb binds TNF-alpha and 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Participants","phase":"","overall_status":"COMPLETED","enrollment_count":5800,"lead_sponsor_name":"Bristol-Myers Squibb","has_results":false},{"nct_id":"NCT04190758","title":"GOTHA - The Early Arthritis and Psoriasis Study of Region Västra Götaland, Sweden","phase":"","overall_status":"ENROLLING_BY_INVITATION","enrollment_count":5100,"lead_sponsor_name":"Vastra Gotaland Region","has_results":false},{"nct_id":"NCT07077304","title":"EACVI Study on Multimodality Cardiovascular Imaging of Inflammatory Cardiovascular Diseases","phase":"","overall_status":"NOT_YET_RECRUITING","enrollment_count":5000,"lead_sponsor_name":"Assistance Publique - Hôpitaux de Paris","has_results":false},{"nct_id":"NCT04402086","title":"Rheumatology Patient Registry and Biorepository","phase":"","overall_status":"RECRUITING","enrollment_count":5000,"lead_sponsor_name":"Yale University","has_results":false},{"nct_id":"NCT04655612","title":"Seroprevalence Study of CoV-2-SARS (COVID-19) Infection in Patients With Chronic Inflammatory Rheumatic Diseases","phase":"","overall_status":"COMPLETED","enrollment_count":5000,"lead_sponsor_name":"University Hospital, Montpellier","has_results":false},{"nct_id":"NCT03470688","title":"Investigating the Utilisation and Effectiveness of Originator and Biosimilar Anti-TNF Agents","phase":"","overall_status":"UNKNOWN","enrollment_count":5000,"lead_sponsor_name":"Opal Rheumatology Ltd.","has_results":false},{"nct_id":"NCT04340115","title":"Study To Assess Frequency Of Serious Infections In Clinical Practice In Japan For Adult Participants With Rheumatoid Arthritis Receiving Oral RINVOQ Tablets","phase":"","overall_status":"COMPLETED","enrollment_count":4211,"lead_sponsor_name":"AbbVie","has_results":false},{"nct_id":"NCT07363980","title":"Coronary Computed Tomography Angiography In Rheumatoid Arthritis Study","phase":"","overall_status":"ENROLLING_BY_INVITATION","enrollment_count":4000,"lead_sponsor_name":"Ellen Margrethe Hauge","has_results":false}],"total":50},"guidelines":[{"drug_id":"azulfidine-en-tabs","guideline_body":"FDA label","recommendation":"Sulfasalazine is indicated for the treatment of rheumatoid arthritis.","line_of_therapy":"1L|2L","evidence_grade":"B","guideline_year":null},{"drug_id":"xeljanz","guideline_body":"FDA label","recommendation":"XELJANZ tablets and XELJANZ XR are indicated for the treatment of adult patients with moderately to severely active rheumatoid arthritis (RA), who have had an inadequate response or intolerance to one or more TNF blockers.","line_of_therapy":"2L","evidence_grade":"not specified","guideline_year":null},{"drug_id":"xeljanz","guideline_body":"FDA label","recommendation":"XELJANZ tablets and XELJANZ XR are indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (UC), who have had an inadequate response or intolerance to one or more TNF blockers.","line_of_therapy":"2L","evidence_grade":"not specified","guideline_year":null},{"drug_id":"xeljanz-xr","guideline_body":"FDA label","recommendation":"XELJANZ tablets and XELJANZ XR are indicated for the treatment of adult patients with moderately to severely active rheumatoid arthritis (RA), who have had an inadequate response or intolerance to one or more TNF blockers.","line_of_therapy":"2L","evidence_grade":"not specified","guideline_year":null},{"drug_id":"adalimumab","guideline_body":"FDA label","recommendation":"Reducing signs and symptoms, inducing major clinical response, inhibiting the progression of structural damage, and improving physical function in adult patients with moderately to severely active rheumatoid arthritis.","line_of_therapy":"1L|2L","evidence_grade":"not specified","guideline_year":null},{"drug_id":"inflectra","guideline_body":"FDA label","recommendation":"reducing signs and symptoms, inhibiting the progression of structural damage, and improving physical function in adult patients with moderately to severely active disease in combination with methotrexate.","line_of_therapy":"2L","evidence_grade":"not specified","guideline_year":null},{"drug_id":"abrilada","guideline_body":"FDA label","recommendation":"Reducing signs and symptoms, inducing major clinical response, inhibiting the progression of structural damage, and improving physical function in adult patients with moderately to severely active rheumatoid arthritis.","line_of_therapy":"1L|2L","evidence_grade":"not specified","guideline_year":null},{"drug_id":"etanercept","guideline_body":"FDA label","recommendation":"Enbrel is indicated for reducing signs and symptoms, inducing major clinical response, inhibiting the progression of structural damage, and improving physical function in patients with moderately to severely active rheumatoid arthritis (RA). Enbrel can be initiated in combination with methotrexate (MTX) or used alone.","line_of_therapy":"1L","evidence_grade":"A","guideline_year":null},{"drug_id":"etanercept","guideline_body":"FDA label","recommendation":"Enbrel is indicated for reducing signs and symptoms of moderately to severely active polyarticular juvenile idiopathic arthritis (pJIA) in patients 2 years of age and older.","line_of_therapy":"1L","evidence_grade":"A","guideline_year":null},{"drug_id":"etanercept","guideline_body":"FDA label","recommendation":"Enbrel is indicated for reducing signs and symptoms, inhibiting the progression of structural damage of active arthritis, and improving physical function in adult patients with psoriatic arthritis (PsA). Enbrel can be used with or without methotrexate.","line_of_therapy":"1L","evidence_grade":"A","guideline_year":null},{"drug_id":"etanercept","guideline_body":"FDA label","recommendation":"Enbrel is indicated for reducing signs and symptoms in patients with active ankylosing spondylitis (AS).","line_of_therapy":"1L","evidence_grade":"A","guideline_year":null},{"drug_id":"tofacitinib","guideline_body":"FDA label","recommendation":"XELJANZ tablets and XELJANZ XR are indicated for the treatment of adult patients with moderately to severely active rheumatoid arthritis (RA), who have had an inadequate response or intolerance to one or more TNF blockers.","line_of_therapy":"2L","evidence_grade":"not specified","guideline_year":null},{"drug_id":"upadacitinib","guideline_body":"FDA label","recommendation":"RINVOQ is indicated for the treatment of adults with moderately to severely active rheumatoid arthritis who have had an inadequate response or intolerance to one or more TNF blockers.","line_of_therapy":"2L","evidence_grade":"not specified","guideline_year":null},{"drug_id":"upadacitinib","guideline_body":"FDA label","recommendation":"RINVOQ is indicated for the treatment of adults with moderately to severely active ulcerative colitis who have had an inadequate response or intolerance to one or more TNF blockers. If TNF blockers are clinically inadvisable, patients should have received at least one approved systemic therapy prior to use of RINVOQ.","line_of_therapy":"2L","evidence_grade":"not specified","guideline_year":null},{"drug_id":"upadacitinib","guideline_body":"FDA label","recommendation":"RINVOQ is indicated for the treatment of adults with active ankylosing spondylitis who have had an inadequate response or intolerance to one or more TNF blockers.","line_of_therapy":"2L","evidence_grade":"not specified","guideline_year":null},{"drug_id":"upadacitinib","guideline_body":"FDA label","recommendation":"RINVOQ is indicated for the treatment of adults with moderately to severely active Crohn’s disease who have had an inadequate response or intolerance to one or more TNF blockers. If TNF blockers are clinically inadvisable, patients should have received at least one approved systemic therapy prior to use of RINVOQ.","line_of_therapy":"2L","evidence_grade":"not specified","guideline_year":null},{"drug_id":"upadacitinib","guideline_body":"FDA label","recommendation":"RINVOQ is indicated for the treatment of adults with active non-radiographic axial spondyloarthritis with objective signs of inflammation who have had an inadequate response or intolerance to TNF blocker.","line_of_therapy":"2L","evidence_grade":"not specified","guideline_year":null},{"drug_id":"daypro","guideline_body":"FDA label","recommendation":"For relief of the signs and symptoms of rheumatoid arthritis","line_of_therapy":"1L","evidence_grade":"B","guideline_year":null},{"drug_id":"abatacept","guideline_body":"FDA label","recommendation":"ORENCIA is indicated for the treatment of adult patients with moderately to severely active rheumatoid arthritis (RA).","line_of_therapy":"any","evidence_grade":"not specified","guideline_year":null},{"drug_id":"dexketoprofen","guideline_body":"FDA label","recommendation":"Ketoprofen extended-release capsules are indicated for the management of the signs and symptoms of rheumatoid arthritis.","line_of_therapy":"any","evidence_grade":"B","guideline_year":null},{"drug_id":"dexketoprofen","guideline_body":"FDA label","recommendation":"Ketoprofen extended-release capsules are indicated for the management of the signs and symptoms of osteoarthritis.","line_of_therapy":"any","evidence_grade":"B","guideline_year":null}],"source":"Drug Landscape verified database"}