Intervention
adalimumab
ClinicalTrials.gov intervention label
How to interpret these research links
Connected source recordsThis is the original ClinicalTrials.gov intervention label, found in 34 distinct published trials. Registry interventions may represent drugs, devices, procedures or other study activities. A matched term or study association does not establish product equivalence, efficacy or regulatory approval.
Data basis: current published ClinicalTrials.gov records and, where present, RxNorm, MONDO and FDA-label identifiers. See the evidence interpretation and counting methodology.
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Clinical trials
34 shownA Comparative Study Between PF-06410293 and Humira® in Combination With Methotrexate in Participants With Active Rheumatoid ArthritisNCT04230213 · 2020-01-13
COMPLETEDA Study Comparing Biologics + Methotrexate With Biologics + Tacrolimus in Patients With Rheumatoid Arthritis (RA)NCT03737708 · 2019-02-13
COMPLETEDTreatment Tapering in JIA With Inactive DiseaseNCT02840175 · 2017-05-18
COMPLETEDPredictability Studies on the Efficacy of TNF-α Inhibitors in Chinese RA From "Real World"NCT02878161 · 2016-01-01
UNKNOWNA Study to Investigate the Safety and Efficacy of ABT-122 Given With Methotrexate in Subjects With Active Rheumatoid Arthritis Who Have an Inadequate Response to MethotrexateNCT02141997 · 2014-07-01
COMPLETEDSafety Study Of Tofacitinib Versus Tumor Necrosis Factor (TNF) Inhibitor In Subjects With Rheumatoid ArthritisNCT02092467 · 2014-03-14
COMPLETEDA Study of RoActemra/Actemra (Tocilizumab) Versus Adalimumab in Combination With Methotrexate (MTX) in Patients With Moderate to Severe Active Rheumatoid Arthritis And an Inadequate Response to Treatment With Only One Tumor Necrosis Factor (TNF)-InhibitorNCT01283971 · 2011-05-01
TERMINATEDREstore Working Ability in RheumatoiD ArthritisNCT01405326 · 2011-05-01
UNKNOWNSerum Concentration of Adalimumab as a Predictive Factor of Clinical Outcomes in Rheumatoid Arthritis (AFORA)NCT01382160 · 2011-01-01
COMPLETEDA Study to Evaluate the Efficacy and Safety of MLTA3698A in Combination With a Disease-Modifying Anti-Rheumatic Drug (DMARD) Compared With Adalimumab in Combination With a DMARD in Patients With Active Rheumatoid ArthritisNCT01225393 · 2010-11-01
COMPLETEDPain Modulation in Rheumatoid Arthritis (RA) - Influence of AdalimumabNCT01197144 · 2010-10-01
COMPLETEDStudy to Determine the Effects of Different Doses of Methotrexate (MTX) When Taken With Adalimumab in Subjects With Early Rheumatoid Arthritis (RA)NCT01185301 · 2010-10-01
COMPLETEDA Canadian Study to Evaluate Early Use of Adalimumab After Methotrexate Failure in Early Rheumatoid ArthritisNCT01162421 · 2010-09-01
COMPLETEDIntravitreal Adalimumab in Refractory Diabetic Retinopathy, Choroidal Neovascularization or Uveitis: A Pilot StudyNCT00855608 · 2009-03-01
UNKNOWNA Pilot Study of the Feasibility of Discontinuation of Adalimumab in Stable Rheumatoid Arthritis Patients in Clinical RemissionNCT00808509 · 2009-01-01
COMPLETEDA Study of Immune Cells in Patients With Rheumatoid Arthritis During Different Types of Anti-TNF Alpha Treatments (Study P05521)NCT00724672 · 2008-09-01
WITHDRAWNA Study of Adalimumab When Added to Inadequate Standard Anti-rheumatic Therapy in Patients With Active Rheumatoid ArthritisNCT01231321 · 2007-12-01
COMPLETEDStudy Comparing 80 mg of Adalimumab With Placebo, and Demonstrating the Non-inferiority of Monthly 80 mg Adalimumab Dosing Compared With 40 mg Adalimumab Every Other Week DosingNCT00647270 · 2007-12-01
COMPLETEDPharmacokinetic and Safety Study With Adalimumab in Chinese Subjects With Mild Rheumatoid ArthritisNCT00650156 · 2007-06-01
COMPLETEDStudy of the Optimal Protocol for Methotrexate and Adalimumab Combination Therapy in Early Rheumatoid ArthritisNCT00420927 · 2006-12-01
COMPLETEDPositron Emission Tomography in Rheumatoid Arthritis With Adalimumab (PETRA)NCT00497614 · 2006-05-01
COMPLETEDAdalimumab in Adult Japanese Subjects With Rheumatoid ArthritisNCT00235872 · 2004-08-01
COMPLETEDEfficacy of HUMIRA in Subjects With Active Rheumatoid ArthritisNCT00234897 · 2004-08-01
COMPLETEDA Study of Adalimumab in Adult Japanese Subjects With Rheumatoid ArthritisNCT00647491 · 2004-02-01
COMPLETEDAssessment of the Effect of Adalimumab on Response to Influenza Virus and Pneumococcal Vaccines in Subjects With Rheumatoid ArthritisNCT00649922 · 2003-10-01
COMPLETEDPost-marketing Observational Study in Subjects With Rheumatoid ArthritisNCT00234884 · 2003-09-01
COMPLETEDStudy of Adalimumab Administered as Subcutaneous Injections in Adult Chinese Rheumatoid Arthritis Subjects Treated With MethotrexateNCT00647920 · 2003-07-01
COMPLETEDAdalimumab Administered in Korean Rheumatoid Arthritis Subjects Treated With MethotrexateNCT00235859 · 2003-07-01
COMPLETEDAdalimumab in Adult Japanese Subjects With Rheumatoid ArthritisNCT00235833 · 2003-06-01
COMPLETEDAdalimumab in Combination With Methotrexate vs Methotrexate Alone in Early Rheumatoid ArthritisNCT00234845 · 2003-03-01
COMPLETEDA Study to Assess the Safety and Efficacy of Adalimumab When Added to Inadequate Standard Anti-Rheumatic Therapy in Patients With Active Rheumatoid ArthritisNCT00448383 · 2002-09-01
COMPLETEDEarly Access Program of the Safety of Human Anti-TNF Monoclonal Antibody Adalimumab in Subjects With Active Rheumatoid ArthritisNCT00650026
APPROVED_FOR_MARKETINGOpen Label Study to Assess Efficacy and Safety of the Fully Human Anti-TNF-Alpha Monoclonal Antibody AdalimumabNCT00650390
APPROVED_FOR_MARKETINGStudy of the Human Anti-TNF Monoclonal Antibody in Patients With Active Rheumatoid ArthritisNCT00649545
APPROVED_FOR_MARKETINGCommon conditions
Leading sponsors
Abbott
16
AbbVie (prior sponsor, Abbott)
3
AbbVie
2
Pfizer
2
University Hospital, Tours
2
Assistance Publique - Hôpitaux de Paris
1
Astellas Pharma Korea, Inc.
1
Fen Li
1
Genentech, Inc.
1
Hoffmann-La Roche
1
Karolinska Institutet
1
Merck Sharp & Dohme LLC
1
Rafic Hariri University Hospital
1
The Rheumatological Center of Helsinki
1
Trial status mix
COMPLETED26
APPROVED_FOR_MARKETING3
UNKNOWN3
TERMINATED1
WITHDRAWN1
Phase mix
PHASE311
PHASE411
PHASE24
NA2
PHASE12
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Registry-derived research relationships: ClinicalTrials.gov. Raw condition and intervention labels remain distinct from canonical MONDO/RxNorm entities unless separately normalized.