Adalimumab

drug
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Also known as Abp-501AbriladaAdalimumab (abbvie)Adalimumab (genetical recombination)Adalimumab (humira)Adalimumab aacfAdalimumab adazAdalimumab adbmAdalimumab afzbAdalimumab aqvhAdalimumab attoAdalimumab betaAdalimumab biosimilar (alvotech)Adalimumab biosimilar (amgen)Adalimumab biosimilar (avt02)Adalimumab biosimilar (celltrion)Adalimumab biosimilar (ct-p17)Adalimumab biosimilar (fkb-327)Adalimumab biosimilar (msb11022)

Summary

Adalimumab (CHEMBL1201580) is an approved antibody (ATC L04AB04); indicated across 37 conditions including ankylosing spondylitis and psoriasis.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Antibody
  • ATC class: L04AB04
  • Indications: 37 conditions
  • Clinical trials: 443

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1201580
NameAdalimumab
TypeAntibody
Max phase4
ATCL04AB04

Also known as: Abp-501, Abrilada, Adalimumab, Adalimumab (abbvie), Adalimumab (genetical recombination), Adalimumab (humira), Adalimumab aacf, Adalimumab adaz, Adalimumab adbm, Adalimumab afzb, Adalimumab aqvh, Adalimumab atto

Targets

Targets

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

12 approved indications. FDA phase 4, plus an anticancer drug’s labelled cancer uses (which ChEMBL often logs at phase 3).

IndicationPhaseMONDOEFO
ankylosing spondylitis4MONDO:0005306EFO:0003898
psoriasis4MONDO:0005083EFO:0000676
rheumatoid arthritis4MONDO:0008383EFO:0000685
ulcerative colitis4MONDO:0005101EFO:0000729
Crohn disease4MONDO:0005011EFO:0000384
psoriatic arthritis4MONDO:0011849EFO:0003778
juvenile idiopathic arthritis4MONDO:0011429EFO:0002609
hidradenitis suppurativa4MONDO:0006559EFO:1000710
uveitis4MONDO:0020283EFO:1001231
immune system disorder4MONDO:0005046EFO:0000540
arthritic joint disease4MONDO:0005578EFO:0005856
psoriasis-related juvenile idiopathic arthritis4MONDO:0019436EFO:0009733

22 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.

Disease (in trials)PhaseMONDOEFO
pyoderma3MONDO:0002922HP:0000999
Behcet disease3MONDO:0007191EFO:0003780
temporal arteritis3MONDO:0008538EFO:1001209
interstitial cystitis3MONDO:0018301EFO:0008507
severe acute respiratory syndrome3MONDO:0005091MONDO:0100096
inflammatory bowel disease3MONDO:0005265EFO:0003767
osteoarthritis3MONDO:0005178MONDO:0005178
spondyloarthropathy3MONDO:0005095EFO:0000706
focal segmental glomerulosclerosis2MONDO:0100313EFO:0004236
colitis2MONDO:0005292EFO:0003872
palmar fibromatosis2MONDO:0006345EFO:0004229
sciatica2MONDO:0024333HP:0011868
osteoarthritis, knee2MONDO:0005416EFO:0004616
frozen shoulder2MONDO:0006763EFO:1000941
asthma2MONDO:0004979MONDO:0004979
Netherton syndrome2MONDO:0009735MONDO:0009735
sarcoidosis2MONDO:0019338MONDO:0019338
benign prostatic hyperplasia2MONDO:0010811EFO:0000284
age-related macular degeneration2MONDO:0005150EFO:0001365
choroidal neovascularization2MONDO:0810000MONDO:0810000
mucopolysaccharidosis type 61MONDO:0009661MONDO:0009661
mucopolysaccharidosis type 21MONDO:0010674MONDO:0010674

3 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 443.

Phase distribution

PhaseTrials
PHASE3156
PHASE4103
PHASE268
Not specified68
PHASE133
PHASE2/PHASE39
PHASE1/PHASE25
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03917303PHASE4RECRUITINGControl Crohn Safe Trial
NCT04183608PHASE4RECRUITINGA Trial COmparing staNdard of Care Versus Treat to Target With telemonitoRing and Patient Education in Patients With Ulcerative cOlitis Initiating Adalimumab
NCT04300686PHASE4RECRUITINGA Pilot Study in Severe Patients With Takayasu Arteritis.
NCT04646187PHASE4ENROLLING_BY_INVITATIONDe-escalation of Anti-TNF Therapy in Inflammatory Bowel Disease
NCT05626348PHASE4RECRUITINGThe Clinical Efficacy of Immunomodulators in RA Patients
NCT06045754PHASE4RECRUITINGA Study of Vedolizumab Intravenous (IV) and Adalimumab or Vedolizumab and Ustekinumab in Adults With Crohn’s Disease
NCT06180382PHASE4RECRUITINGComparison of Vedolizumab Treatment to Adalimumab Dose Intensification in Crohn’s Disease Patients With Loss of Response or Biomarker Activity to Adalimumab on First Line With Therapeutic Drug Concentration.
NCT06390436PHASE4NOT_YET_RECRUITINGTherapeutic Drug Monitoring-baSed adalimuMab De-escalatiOn in nOn-infecTious cHronic Uveitis
NCT06498089PHASE4RECRUITINGA Randomized, Controlled, Open-label, Multicenter Clinical Trial Comparing the Efficacy and Safety of a Precision Treatment Regimen Based on Clinical-molecular Phenotypes with a Conventional Treatment Regimen in the Treatment of Patients with Active Takayasu’s Arteritis
NCT06527534PHASE4RECRUITINGFilgotinib Effect on Proteomic Profile and Micro-RNA Expression in Patients With Active Rheumatoid Arthritis (RA)
NCT06833112PHASE4NOT_YET_RECRUITINGInterleukin-17 (IL-17) Inhibitor in Combination With Tumor Necrosis Factor α (TNFα )Inhibitor for the Treatment of Ankylosing Spondylitis
NCT07013838PHASE4NOT_YET_RECRUITINGThe Efficacy and Safety of Deucravacitinib in Takayasu’s Arteritis
NCT07352566PHASE4NOT_YET_RECRUITINGUtilization of a Microdevice for Psoriasis and Atopic Dermatitis
NCT07510191PHASE4RECRUITINGTNFi Plus Low-Dose Upadacitinib vs TNFi Intensification in Crohn’s Disease With Suboptimal Response
NCT07529925PHASE4NOT_YET_RECRUITINGA Clinical Trail of Adalimumab in Treating Chinese Children With Severe Plaque Psoriasis
NCT07564505PHASE4NOT_YET_RECRUITINGPost - Marketing Case Registration Study on the Safety and Efficacy of Adalimumab Solution for Injection in Chinese Pediatric Patients With Moderate - to - Severe Active Crohn’s Disease
NCT00133315PHASE4COMPLETEDTNFalfa Blocking Treatment of Spondylarthropathies
NCT00216177PHASE4UNKNOWNComparison of Adalimumab and Infliximab Treatment of Rheumatoid Arthritis
NCT00234234PHASE4COMPLETEDPredictors of the Response to Adalimumab in Rheumatoid Arthritis
NCT00234897PHASE4COMPLETEDEfficacy of HUMIRA in Subjects With Active Rheumatoid Arthritis
NCT00291915PHASE4UNKNOWNMulticenter Randomized Prospective Trial Comparing Methotrexate Alone or in Combination With Adalimumab in Early Arthritis
NCT00420927PHASE4COMPLETEDStudy of the Optimal Protocol for Methotrexate and Adalimumab Combination Therapy in Early Rheumatoid Arthritis
NCT00477893PHASE4UNKNOWNDanish Multicenter Study of Adalimumab in Spondyloarthritis
NCT00480272PHASE4COMPLETEDProspective Study on Intensive Early Rheumatoid Arthritis Treatment
NCT00517296PHASE4COMPLETEDEndoscopic Ultrasound (EUS) Guided Treatment With Humira for Crohn’s Perianal Fistulas
NCT00649922PHASE4COMPLETEDAssessment of the Effect of Adalimumab on Response to Influenza Virus and Pneumococcal Vaccines in Subjects With Rheumatoid Arthritis
NCT00696059PHASE4COMPLETEDHumira in Rheumatoid Arthritis - Do Bone Erosions Heal?
NCT00735787PHASE4COMPLETEDControlled Study of Humira in Subjects With Chronic Plaque Psoriasis of the Hands and/or Feet
NCT00761514PHASE4TERMINATEDEvaluation of Quality of Life Changes in Puerto Rican Subjects With Active Rheumatoid Arthritis Treated With Humira
NCT00796705PHASE4TERMINATEDSwitching Anti-TNF-Alpha Agents in Rheumatoid Arthritis (RA)
NCT00808509PHASE4COMPLETEDA Pilot Study of the Feasibility of Discontinuation of Adalimumab in Stable Rheumatoid Arthritis Patients in Clinical Remission
NCT00837434PHASE4COMPLETEDAnti-TNF Agents for the Treatment of Rheumatoid Arthritis
NCT00932113PHASE4COMPLETEDMechanism of Action Study for Psoriasis
NCT00940862PHASE4COMPLETEDEffect of Adalimumab on Vascular Inflammation in Patients With Moderate to Severe Plaque Psoriasis
NCT00972218PHASE4WITHDRAWNEffectiveness and Safety of Spondylitis Related to Inflammatory Bowel Disease
NCT01000441PHASE4COMPLETEDRotation or Change of Biotherapy After First Anti-TNF Treatment Failure for Rheumatoid Arthritis
NCT01029847PHASE4COMPLETEDAdalimumab in Axial Spondyloarthritis (ASIM) - MRI and Biomarkers in Patients With Spondyloarthritis
NCT01072058PHASE4UNKNOWNHeart Function in Rheumatoid Arthritis and Ankylosing Spondylitis Pre and Post-TNF Blocker
NCT01119859PHASE4COMPLETEDA Study of Tocilizumab (RoActemra/Actemra) Versus Adalimumab in Patients With Rheumatoid Arthritis
NCT01162421PHASE4COMPLETEDA Canadian Study to Evaluate Early Use of Adalimumab After Methotrexate Failure in Early Rheumatoid Arthritis
NCT01174186PHASE4COMPLETEDIntestinal Inflammation in Ankylosing Spondylitis and the Effects of Adalimumab on Mucosal Healing
NCT01181570PHASE4COMPLETEDEfficacy and Safety of Adalimumab in Patients With Psoriasis and Obstructive Sleep Apnea
NCT01185288PHASE4COMPLETEDA Study to Determine the Effect of Methotrexate (MTX) Dose on Clinical Outcome and Ultrasonographic Signs in Subjects With Moderately to Severely Active Rheumatoid Arthritis (RA) Treated With Adalimumab (MUSICA)
NCT01237262PHASE4UNKNOWNEvaluation of Lymphocytic Infiltrate, Dendritic Cells and Cytokines Expression in Psoriatic Lesion and Normal Skin Before and After TNF Alfa Inhibitors Therapy
NCT01265823PHASE4COMPLETEDImmediate Response With Adalimumab and Its Impact on Quality of Life and Other Comorbidity Factors in Patients With Moderate to Severe Plaque Psoriasis
NCT01270035PHASE4UNKNOWNEfficacy and Safety of Adalimumab 80 mg Every Other Week With Methotrexate
NCT01270087PHASE4COMPLETEDThe Effect of Adalimumab (Humira) on Vascular Abnormalities in Rheumatoid Arthritis. A Pilot Study.
NCT01283971PHASE4TERMINATEDA 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)-Inhibitor
NCT01295151PHASE4COMPLETEDSWITCH Clinical Trial for Patients With Rheumatoid Arthritis Who Have Failed an Initial TNF-blocking Drug.
NCT01382160PHASE4COMPLETEDSerum Concentration of Adalimumab as a Predictive Factor of Clinical Outcomes in Rheumatoid Arthritis (AFORA)
NCT01405326PHASE4UNKNOWNREstore Working Ability in RheumatoiD Arthritis
NCT01465438PHASE4COMPLETEDHUmira in Psoriatic Arthritis
NCT01500278PHASE4COMPLETEDStudy to Assess the Short- and Long-term Efficacy of Certolizumab Pegol Plus Methotrexate Compared to Adalimumab Plus Methotrexate in Subjects With Moderate to Severe Rheumatoid Arthritis (RA) Inadequately Responding to Methotrexate
NCT01553058PHASE4COMPLETEDVascular Inflammation in Psoriasis Trial (The VIP Trial)
NCT01556672PHASE4COMPLETEDAdalimumab-psoriasis and Small Bowel Lesions
NCT01602302PHASE4TERMINATEDUltrasound and Withdrawal of Biological DMARDs in Rheumatoid Arthritis
NCT01609205PHASE4COMPLETEDDoppler Evaluation in RA Patients After Adalimumab.
NCT01644396PHASE4COMPLETEDAn Open-Label, Prospective Study to Assess the Safety and Effectiveness of Adalimumab in Patients With Moderate to Severe Plaque Psoriasis in the Russian Federation
NCT01722214PHASE4COMPLETEDTrial on the Effect of Adalimumab on Vascular Inflammation in Patients With Psoriasis
NCT01793519PHASE4UNKNOWNStopping TNF Alpha Inhibitors in Rheumatoid Arthritis
NCT01866592PHASE4COMPLETEDVascular Inflammation in Psoriasis - Extension Study
NCT01893996PHASE4COMPLETEDStudy of Adalimumab to Lower Cardiovascular Risk in RA Patients With Well Controlled Joint Disease
NCT01895764PHASE4COMPLETEDEffect of the Combination of Methotrexate and Adalimumab on Reduction of Immunization in Ankylosing Spondylitis (COMARIS)
NCT02035800PHASE4UNKNOWNBone Resorption, Osteoclastogenesis and Adalimumab
NCT02056184PHASE4COMPLETEDTargeted Ultrasound in Rheumatoid Arthritis
NCT02092467PHASE4COMPLETEDSafety Study Of Tofacitinib Versus Tumor Necrosis Factor (TNF) Inhibitor In Subjects With Rheumatoid Arthritis
NCT02132234PHASE4UNKNOWNEffects of Biological Treatment on Blood Pressure and Endothelial Function in Patients With Rheumatoid Arthritis, Psoriatic Arthritis and Ankylosing Spondylitis
NCT02148718PHASE4COMPLETEDRapidity of Response to Adalimumab Treatment in Patients With Crohn´s Disease
NCT02198651PHASE4COMPLETEDA Phase 4 Trial Assessing the ImPact of Residual Inflammation Detected Via Imaging TEchniques, Drug Levels and Patient Characteristics on the Outcome of Dose TaperIng of Adalimumab in Clinical Remission Rheumatoid ArThritis (RA) Subjects
NCT02256462PHASE4COMPLETEDPediatric Crohn’s Disease AdalImumab Level-based Optimization Treatment (PAILOT) Trial
NCT02374021PHASE4COMPLETEDTreatments Against RA and Effect on FDG-PET/CT
NCT02451748PHASE4COMPLETEDIL-7 and IL-7R Expression in RA Patients With Active vs. Inactive Disease Treated With DMARD or CIMZIA
NCT02489760PHASE4UNKNOWNEtanercept Versus Adalimumab in the Treatment of Patients With Ankylosing Spondylitis. A Switch Study
NCT02492217PHASE4COMPLETEDBiomarkers Identification of Anti-tumor Necrosis Factor (TNF) α Agent’s Efficacy in Ankylosing Spondylitis Patients
NCT02557100PHASE4COMPLETEDStudy to Assess Changes in the Immune Profile in Adults With Early Rheumatoid Arthritis
NCT02634541PHASE4UNKNOWNAdalimumab in Alleviating Inflammation in Patients With Axial Spondyloarthritis
NCT02764762PHASE4COMPLETEDTriple Combination Therapy in High Risk Crohn’s Disease (CD)
NCT02808975PHASE4COMPLETEDSafety and Efficacy of Adalimumab (Humira) for Hidradenitis Suppurativa (HS) Peri-Surgically
NCT02814175PHASE4COMPLETEDA Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness of Adalimumab Introduction Compared With Methotrexate Dose Escalation (CONTROL)
NCT02852694PHASE4COMPLETEDReduce Risk for Crohn’s Disease Patients
NCT02878161PHASE4UNKNOWNPredictability Studies on the Efficacy of TNF-α Inhibitors in Chinese RA From Real World
NCT02897115PHASE4TERMINATEDA Study Treating Participants With Early Axial Spondyloarthritis (axSpA) Taking an Intense Treatment Approach Versus Routine Treatment
NCT03059849PHASE4WITHDRAWNBrief Escalation of Adalimumab Treatment for Prevention of Clinical Relapse in IBD
NCT03100253PHASE4TERMINATEDRheumatoid Arthritis Treatment After First Anti-TNF INvestiGation
NCT03151551PHASE4COMPLETEDA Study of Ixekizumab (LY2439821) Versus Adalimumab in Participants With Psoriatic Arthritis
NCT03220841PHASE4UNKNOWNStricture Definition and Treatment (STRIDENT) Drug Therapy Study
NCT03221621PHASE4UNKNOWNCost-effectiveness of Adalimumab and Surgery vs Adalimumab in HS
NCT03505008PHASE4COMPLETEDEvaluation of the Optimal MTX Dose as an Add-on Therapy to Adalimumab for RA Patients in Japan, South Korea and Taiwan
NCT03619876PHASE4TERMINATEDEffects of Abatacept on Myocarditis in Rheumatoid Arthritis
NCT03737708PHASE4COMPLETEDA Study Comparing Biologics + Methotrexate With Biologics + Tacrolimus in Patients With Rheumatoid Arthritis (RA)
NCT03739853PHASE4COMPLETEDSevere Psoriatic Arthritis - Early intervEntion to Control Disease: the SPEED Trial
NCT03816397PHASE4COMPLETEDAdalimumab in JIA-associated Uveitis Stopping Trial
NCT04132388PHASE4WITHDRAWNHidradenitis Suppurativa Patient Experience With Humira Treatment
NCT04194827PHASE4UNKNOWNAdalimumab Drug Optimisation in Rheumatoid Arthritis Using Therapeutic Drug Monitoring
NCT04222920PHASE4COMPLETEDAdalimumab Dose Reduction Aiming Low Serum Concentration With Control of Disease Activity
NCT04255134PHASE4COMPLETEDBiologics for Rheumatoid Arthritis Pain (BIORA-PAIN)
NCT05015335PHASE4UNKNOWNThe Efficacy and Safety of Adalimumab in Non-infectious Anterior Pediatric Uveitis With Peripheral Vascular Leakage
NCT05151848PHASE4UNKNOWNComparison of Adalimumab and Tofacitinib in the Treatment of Active Takayasu Arteritis
NCT05153200PHASE4UNKNOWNEarly Changes in Pain, Disease Activity, and Ultrasound Evidence of Inflammatory Synovitis in Patients Receiving JAK-inhibitor vs. TNF-inhibitor Therapy for Active Rheumatoid Arthritis: A Feasibility Study.
NCT05164198PHASE4UNKNOWNREduCed Dose of TNFi in Patients With Ankylosing SpondyliTis (RECAST)

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).