| Rheumatoid Arthritis | NCT07554820 | Major Adverse Cardiovascular Events (MACE) in Rheumatoid Arthritis Patient With Moderate to Severe Disease Activity Treated With Tofacitinib and Statins vs TNF Inhibitors: TOFSTAT CLINICAL TRIAL | recruiting | PHASE4 | 120 |
| NCT06979271 | Efficacy and Safety of Telitacicept Combined With Tofacitinib for Refractory Rheumatoid Arthritis | recruiting | N/A | 20 |
| NCT06301373 | Methotrexate Combined With Tofacitinib in Rheumatoid Arthritis | recruiting | NA | 130 |
| NCT06418529 | A Study to Understand How Effective is Tofacitinib When Compared to Other Advanced Treatments in Patients With Rheumatoid Arthritis | completed | N/A | 21,340 |
| NCT06020144 | A Phase 3 Study Comparing TLL-018 to Tofacitinib in RA Subjects With Inadequate Response or Intolerance to bDMARDs | active not recruiting | PHASE3 | 459 |
| NCT05803135 | Iguratimod Combined With Tofacitinib in the Treatment of Rheumatoid Arthritis | unknown | PHASE4 | 138 |
| NCT05246293 | Tofacitinib in the Treatment of Rheumatoid Arthritis-related Interstitial Lung Disease. | unknown | PHASE2 | 60 |
| NCT05165771 | Study to Evaluate Safety, Tolerability, and Efficacy of GS-5718 in Participants With Active Rheumatoid Arthritis Who Have an Inadequate Response to Disease-modifying Antirheumatic Drug(s) (bDMARDs) Treatment | withdrawn | PHASE2 | 0 |
| NCT05606107 | To Compare the Efficacy and Safety of Low-dose Glucocorticoids and Tofacitinib in Alleviating Moderate to High Disease Activity Rheumatoid Arthritis for 24 Weeks | unknown | PHASE4 | 230 |
| NCT05133297 | The Safety and Efficacy of TLL-018 in Active Rheumatoid Arthritis | completed | PHASE2 | 101 |
| NCT05080218 | COVID-19 VaccinE Response in Rheumatology Patients | completed | PHASE4 | 841 |
| NCT04927000 | The Role of Tofacitinib in Steroid Withdrawal in Rheumatoid Arthritis | unknown | PHASE4 | 170 |
| NCT04798287 | Safety of TofAcitinib in Routine Care Patients With Rheumatoid Arthritis (STAR-RA)-Cancer Endpoints | completed | N/A | 105,711 |
| NCT04772248 | Safety of TofAcitinib in Routine Care Patients With Rheumatoid Arthritis (STAR-RA)- Cardiovascular Endpoints | completed | N/A | 105,711 |
| NCT04311567 | Effects of Tofacitinib vs Methotrexate on Rheumatoid Arthritis Interstitial Lung Disease | terminated | PHASE4 | 3 |
| NCT04529876 | Data Analysis for Drug Repurposing for Effective Alzheimer's Medicines (DREAM) - Tofacitinib vs Abatacept | completed | N/A | 29,464 |
| NCT04413617 | TO ASSESS THE EFFICACY AND SAFETY OF PF-06650833, PF-06651600, AND TOFACITINIB ALONE AND IN COMBINATION IN PARTICIPANTS WITH ACTIVE RHEUMATOID ARTHRITIS WITH AN INADEQUATE RESPONSE TO METHOTREXATE | completed | PHASE2 | 460 |
| NCT04449224 | Comparative Effectiveness of Targeted Therapy in RA Patients | unknown | N/A | 506 |
| NCT03976245 | Advanced Therapeutics in Rheumatoid Arthritis (RA) | recruiting | PHASE4 | 144 |
| NCT04175886 | Effects of Tofacitinib on Body Composition, Bone Mineral Density and Bone Marrow Adiposity in Patients With Rheumatoid Arthritis: the TOFAT Project | completed | N/A | 10 |
| NCT04464642 | Tofacitinib Versus Methotrexate as the First Line DMARD in the Treatment of Rheumatoid Arthritis | unknown | PHASE4 | 110 |
| NCT03868072 | Study to Evaluate the Bioequivalence of Pfizer Korea Inc. "XELJANZ 5Mg Tablet" in Healthy Volunteers | completed | PHASE1 | 40 |
| NCT03755466 | Examination of Efficacy and Safety of Baricitinib in RA Patients | unknown | PHASE2 | 90 |
| NCT03440892 | Effects of Antirheumatic Treatment on Levels of Survivin in Rheumatoid Arthritis Patients | unknown | N/A | 2,500 |
| NCT02996500 | Safety and Efficacy of Pf-06650833 In Subjects With Rheumatoid Arthritis, With An Inadequate Response To Methotrexate | completed | PHASE2 | 269 |
| NCT03011281 | Effectiveness and Safety of Tofacitinib in Korean Patients With Rheumatoid Arthritis | unknown | N/A | 378 |
| NCT02321930 | Musculoskeletal Ultrasound Assessment of Therapeutic Response of Tofacitinib in Rheumatoid Arthritis Patients | completed | PHASE4 | 37 |
| NCT02566967 | An Evaluation of the Optimal Dose of Tofacitinib Needed to Achieve Low Disease Activity (LDA) or Clinical Remission in Patients With Active Rheumatoid Arthritis (RA) as Measured From a Clinical and Structural Perspective | completed | PHASE3 | 20 |
| NCT02281552 | A Study To Evaluate The Safety And Efficacy Of Tofacitinib Modified Release Tablets Compared To Tofacitinib Immediate Release Tablets In Adult Patients With Rheumatoid Arthritis | completed | PHASE3 | 209 |
| NCT02147587 | A Study to Assess Immune Response Following Zoster Vaccination to Subjects With Rheumatoid Arthritis Receiving Tofacitinib or Placebo With Background Methotrexate | completed | PHASE2 | 112 |
| NCT01932372 | Tofacitinib (Xeljanz) Special Investigation for Rheumatoid Arthritis | completed | N/A | 9,968 |
| NCT01741493 | A Study in Healthy Adults and Adult Subjects With Rheumatoid Arthritis to Evaluate the Safety, Tolerability and Pharmacokinetics After Multiple Doses of ABT-494 | completed | PHASE1 | 67 |
| NCT01164579 | Effects of Tofacitinib (CP-690,550) on Magnetic Resonance Imaging (MRI)- Assessed Joint Structure In Early Rheumatoid Arthritis (RA) | completed | PHASE2 | 109 |
| NCT03414502 | Treatment of Rheumatoid Arthritis With DMARDs: Predictors of Response | recruiting | PHASE3 | 400 |
| NCT01745055 | Co-Administration Of Methotrexate And CP-690,550 | completed | PHASE1 | 12 |
| Ulcerative Colitis | NCT06625450 | TOFACITINIB vs TOFACITINIB WITH MESALAMINE IN ULCERATIVE COLITIS | not yet recruiting | PHASE4 | 75 |
| NCT06095128 | A Study of Vedolizumab With Tofacitinib in Adults With Ulcerative Colitis (UC) | recruiting | PHASE4 | 65 |
| NCT05112263 | Tofacitinib Versus Cyclosporine for Steroid Refractory Acute Severe Ulcerative Colitis | unknown | NA | 96 |
| NCT05431283 | Real-world Effectiveness of Tofacitinib on Ulcerative Colitis Associated Spondyloarthropathy | unknown | N/A | 100 |
| NCT05728008 | Retrospective Observational Comparison Study Between Ustekinumab and Tofacitinib as Third Line Therapy in a Multicenter Cohort of Patients With Refractory Ulcerative Colitis. | completed | N/A | 100 |
| NCT05313620 | Effect of Tofacitinib on Coagulation and Platelet Function, and Its Role in Thromboembolic Events | recruiting | PHASE4 | 30 |
| NCT05186623 | Prediction Model for Response to Biologics and Small Molecular Agent for UC | recruiting | N/A | 300 |
| NCT04624230 | Evaluation of Oral Tofacitinib in Children Aged 2 to 17 Years Old Suffering From Moderate to Severe Ulcerative Colitis | active not recruiting | PHASE3 | 118 |
| NCT04424303 | Tofacitinib in Adult Patients With Moderate to Severe Ulcerative Colitis | completed | N/A | 152 |
| NCT04338204 | Observational Study To Assess The Effectiveness and Treatment Adherence Of Tofacitinib of Ulcerative Colitis In Clinical Practice In Sweden | completed | N/A | 102 |
| NCT03885713 | Identification of Predictive Biomarkers for Response to Biologic Therapies and Tofacitinib in Inflammatory Bowel Disease | completed | PHASE4 | 180 |
| NCT01458951 | A Study To Evaluate Both The Efficacy and Safety Profile of CP-690,550 In Patients With Moderately to Severely Active Ulcerative Colitis | completed | PHASE3 | 547 |
| NCT01465763 | A Study Evaluating The Efficacy And Safety Of CP-690,550 In Patients With Moderate To Severe Ulcerative Colitis | completed | PHASE3 | 614 |
| Healthy | NCT04985955 | A Study Validating the Use of Candin as a Challenge Agent in Healthy Participants - Intervention Specific Appendix 3 | completed | PHASE1 | 12 |
| NCT04552197 | A Study of JNJ-64251330 in Healthy Participants | completed | PHASE1 | 36 |
| NCT04338711 | A Study In Adult Healthy Volunteers To Asses Once Daily (QD) Dosing With The Selected Age-Appropriate Modified Release (MR) Formulations | completed | PHASE1 | 23 |
| NCT04111614 | A Study to Demonstrate the Equivalence of the Tofacitinib Oral Solution to the Tablet Formulation in Healthy Participants. | completed | PHASE1 | 12 |
| NCT04403776 | PK and Bioavailability Comparison of Tofacitinib Between a Modified Release and The Immediate Release Formulation | completed | PHASE1 | 26 |
| NCT03112148 | PK Study in Adult Healthy Volunteers to Assess QD Dosing With the Selected Age-appropriate MR Formulations | completed | PHASE1 | 24 |
| NCT02487433 | A Study To Evaluate The Effect Of Food On The Behavior of Tofacitinib Modified Release 22 Milligram Tablets In Healthy Volunteers | completed | PHASE1 | 18 |
| NCT02084875 | A Study To Evaluate The Effect Of Food On The Behavior Of Tofacitinib Modified Release 11 Milligram Tablets In Healthy Western And Japanese Volunteers | completed | PHASE1 | 24 |
| NCT01731327 | A Phase 1 Study To Evaluate The Pharmacokinetics (PK), Safety, And Bioavailability Of A Modified-Release (MR) Formulation Of Tofacitinib In Healthy Volunteers | completed | PHASE1 | 20 |
| NCT01599377 | Tofacitinib Bioequivalence Study Comparing Tablets And Capsules | completed | PHASE1 | 50 |
| NCT01499004 | A Phase 1 Study To Evaluate The Pharmacokinetics And Safety Of Three Modified Release And One Immediate Release Formulations Of Tofacitinib (CP-690,550) In Healthy Volunteers | completed | PHASE1 | 30 |
| Psoriatic Arthritis | NCT07406035 | A Phase II Clinical Trial to Evaluate the Efficacy and Safety of TQH3906 Capsules in the Treatment of Active Psoriatic Arthritis | not yet recruiting | PHASE2 | 156 |
| NCT06176508 | Efficacy and Safety of HS-10374 Compared to Placebo in Adults With Active Psoriatic Arthritis | recruiting | PHASE2 | 160 |
| NCT05080218 | COVID-19 VaccinE Response in Rheumatology Patients | completed | PHASE4 | 841 |
| NCT04610476 | Impact of Tapering Immunosuppressants on Maintaining Minimal Disease Activity in Adult Subjects With Psoriatic Arthritis | unknown | PHASE3 | 270 |
| NCT04062695 | Tofacitinib for Reduction of Spinal Inflammation in Patients With Psoriatic ArthritiS PresenTing With Axial InvOlvement | unknown | PHASE2 | 80 |
| NCT03486457 | Efficacy And Safety Of Tofacitinib In Chinese Subjects With Active Psoriatic Arthritis | completed | PHASE3 | 204 |
| NCT03736161 | Safety and Efficacy of Tofacitinib vs Methotrexate in the Treatment of Psoriatic Arthritis | completed | PHASE3 | 61 |
| NCT01877668 | Efficacy And Safety Of Tofacitinib In Psoriatic Arthritis: Comparator Study | completed | PHASE3 | 422 |
| NCT01882439 | Tofacitinib In Psoriatic Arthritis Subjects With Inadequate Response to TNF Inhibitors | completed | PHASE3 | 395 |
| Alopecia Areata | NCT07406204 | Tofacitinib vs Methotrexate for Severe Alopecia Areata (TOFA-MTX-AA) | not yet recruiting | PHASE4 | 78 |
| NCT06573593 | Efficacy and Safety of JAK Inhibitors in Patients With AA: RWE Study | recruiting | N/A | 150 |
| NCT06278402 | Efficacy of Oral Tofacitinib in Moderate to Severe Alopecia Areata, Totalis and Universalis at Tertiary Care Hospital, Karachi. | completed | PHASE3 | 30 |
| NCT04246372 | Tofacitinib for Immune Skin Conditions in Down Syndrome | completed | PHASE2 | 47 |
| NCT03800979 | Effectiveness and Safety of Tofacitinib in Patients With Extensive and Recalcitrant Alopecia Areata | completed | PHASE4 | 19 |
| NCT02812342 | Topical Tofacitinib for the Treatment of Alopecia Areata and Its Variants | completed | PHASE2 | 10 |
| NCT02299297 | Study To Evaluate The Efficacy Of Tofacitinib In Moderate To Severe Alopecia Areata, Totalis And Universalis | completed | PHASE2 | 12 |
| NCT02312882 | Tofacitinib for the Treatment of Alopecia Areata and Its Variants | completed | NA | 40 |
| Arthritis, Rheumatoid | NCT04928066 | The Efficacy and Safety of Tofacitinib (TF) With Iguratimod (IGU) on RA | completed | PHASE4 | 100 |
| NCT03970837 | Efficacy and Safety of GSK3196165 Versus Placebo and Tofacitinib in Participants With Moderately to Severely Active Rheumatoid Arthritis Who Have an Inadequate Response to Conventional Synthetic (cs)/Biologic (b) Disease Modifying Anti-rheumatic Drugs (DMARDs) | terminated | PHASE3 | 1,764 |
| NCT03980483 | Efficacy and Safety of GSK3196165 Versus Placebo and Tofacitinib in Participants With Moderately to Severely Active Rheumatoid Arthritis Who Have an Inadequate Response to Methotrexate | completed | PHASE3 | 1,537 |
| NCT03981900 | IDentification of Factors Predictive of Tofacitinib's Survival in Patient With Rheumatoid Arthritis | completed | N/A | 314 |
| NCT03387423 | Observational Study to Determine How Physicians Make Treatment Decisions in Patients Treated With Tofacitinib for Moderate to Severe Active Rheumatoid Arthritis | completed | N/A | 1,459 |
| NCT02092467 | Safety Study Of Tofacitinib Versus Tumor Necrosis Factor (TNF) Inhibitor In Subjects With Rheumatoid Arthritis | completed | PHASE4 | 4,372 |
| Psoriasis | NCT07352566 | Utilization of a Microdevice for Psoriasis and Atopic Dermatitis | not yet recruiting | PHASE4 | 10 |
| NCT07261306 | Comparison Between Oral Methotrexate and Tofacitinib in Chronic Plaque Psoriasis | recruiting | EARLY_PHASE1 | 75 |
| NCT04246372 | Tofacitinib for Immune Skin Conditions in Down Syndrome | completed | PHASE2 | 47 |
| NCT01831466 | Tofacitinib Ointment For Chronic Plaque Psoriasis | completed | PHASE2 | 476 |
| NCT01736696 | Multiple Dose Escalation Study In Medically Stable Subjects With Psoriasis | completed | PHASE1 | 59 |
| Takayasu Arteritis | NCT06498089 | A 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 | recruiting | PHASE4 | 124 |
| NCT05749666 | Comparison of Tofacitinib and Prednisolone in the Treatment of Active Takayasu's Arteritis | unknown | PHASE3 | 50 |
| NCT05151848 | Comparison of Adalimumab and Tofacitinib in the Treatment of Active Takayasu Arteritis | unknown | PHASE4 | 100 |
| NCT05102448 | Comparison of Tofacitinib and Methotrexate in Takayasu's Arteritis | recruiting | PHASE4 | 76 |
| NCT04299971 | Efficiency of Methotrexate and Tofacitinib in Mild and Moderate Patients | unknown | PHASE4 | 130 |
| COVID-19 | NCT04412252 | Safety and Efficacy of Tofacitinib in Hospitalized Participants With COVID-19 Pneumonia Who Are Receiving Standard of Care Therapy | withdrawn | PHASE2 | 0 |
| NCT04390061 | TOFAcitinib Plus Hydroxycloroquine vs Hydroxycloroquine in Patients With COVID-19 Interstitial Pneumonia | unknown | PHASE2 | 116 |
| NCT05638932 | Methodologies for Observational Studies Comparing Inpatient COVID-19 Treatments | completed | N/A | 1,442 |
| NCT04750317 | Efficacy and Safety of Tofacitinib in Patients With COVID-19 Pneumonia | completed | PHASE2 | 414 |
| Alopecia Universalis | NCT07406204 | Tofacitinib vs Methotrexate for Severe Alopecia Areata (TOFA-MTX-AA) | not yet recruiting | PHASE4 | 78 |
| NCT06278402 | Efficacy of Oral Tofacitinib in Moderate to Severe Alopecia Areata, Totalis and Universalis at Tertiary Care Hospital, Karachi. | completed | PHASE3 | 30 |
| NCT02812342 | Topical Tofacitinib for the Treatment of Alopecia Areata and Its Variants | completed | PHASE2 | 10 |
| NCT02312882 | Tofacitinib for the Treatment of Alopecia Areata and Its Variants | completed | NA | 40 |
| Systemic Lupus Erythematosus | NCT03288324 | Open-label Study of Tofacitinib for Moderate to Severe Skin Involvement in Young Adults With Lupus | completed | PHASE1/PHASE2 | 13 |
| NCT03159936 | Oral Tofacitinib in Adult Subjects With Discoid Lupus Erythematosus (DLE) and Systemic Lupus Erythematosus (SLE) | terminated | EARLY_PHASE1 | 5 |
| NCT02535689 | Safety of Tofacitinib, an Oral Janus Kinase Inhibitor, in Systemic Lupus Erythematosus | completed | PHASE1 | 34 |
| Axial Spondyloarthritis | NCT06112665 | ToFAcitinib in Early Active Axial SpondyloarThritis: | recruiting | PHASE4 | 104 |
| NCT06310057 | Tofacitinib in the Treatment of Refractory Axial Spondyloarthritis Patients: A Dose Escalation Study | completed | PHASE4 | 92 |
| NCT03738956 | Safety and Efficacy of Tofacitinib in the Treatment of NSAID Refractory Axial Spondyloarthritis:A Clinical Trial | unknown | PHASE2/PHASE3 | 30 |
| Atopic Dermatitis | NCT07352566 | Utilization of a Microdevice for Psoriasis and Atopic Dermatitis | not yet recruiting | PHASE4 | 10 |
| NCT06465732 | Efficacy and Safety of Dupilumab in Combination With Tofacitinib in Moderate to Severe Adult AD Patients | not yet recruiting | PHASE4 | 220 |
| NCT05487963 | Tolerability and Effectiveness of CGB-500 Topical Ointment, 1% Tofacitinib, for the Treatment of Atopic Dermatitis | completed | PHASE1/PHASE2 | 40 |
| Alopecia Totalis | NCT06278402 | Efficacy of Oral Tofacitinib in Moderate to Severe Alopecia Areata, Totalis and Universalis at Tertiary Care Hospital, Karachi. | completed | PHASE3 | 30 |
| NCT02812342 | Topical Tofacitinib for the Treatment of Alopecia Areata and Its Variants | completed | PHASE2 | 10 |
| NCT02312882 | Tofacitinib for the Treatment of Alopecia Areata and Its Variants | completed | NA | 40 |
| Hidradenitis Suppurativa | NCT06707246 | A Randomized Trial Comparing the Efficacy and Safety of Secukinumab with Tofacitinib in the Treatment of Moderate to Severe Hidradenitis Suppurativa in Chinese Patients | recruiting | NA | 60 |
| NCT04246372 | Tofacitinib for Immune Skin Conditions in Down Syndrome | completed | PHASE2 | 47 |
| Active Ankylosing Spondylitis | NCT05814939 | Efficacy and Safety Clinical Study of VC005 Tablets in Subjects With Active Ankylosing Spondylitis. | completed | PHASE2 | 180 |
| NCT04876781 | Korean Post-marketing Surveillance for Xeljanz XR | recruiting | N/A | 200 |
| Ankylosing Spondylitis | NCT03502616 | Efficacy and Safety of Tofacitinib in Subjects With Active Ankylosing Spondylitis (AS) | completed | PHASE3 | 270 |
| NCT01786668 | Dose-Ranging Study Of Tofacitinib In Adults With Active Ankylosing Spondylitis | completed | PHASE2 | 208 |
| Polymyalgia Rheumatica | NCT06172361 | Induction and Tapering Therapy With Tofacitinib and Glucocorticoid in Patients With Polymyalgia Rheumatica | recruiting | PHASE3 | 98 |
| NCT04799262 | Tofacitinib as a GC Sparing Agent for Polymyalgia Rheumatica | completed | PHASE2 | 14 |
| Cutaneous Lupus | NCT05048238 | Evaluation of Tofacitinib in Prevention of Photosensitivity in Lupus | completed | PHASE1 | 7 |
| NCT03288324 | Open-label Study of Tofacitinib for Moderate to Severe Skin Involvement in Young Adults With Lupus | completed | PHASE1/PHASE2 | 13 |
| Juvenile Idiopathic Arthritis | NCT02592434 | Efficacy Study Of Tofacitinib In Pediatric JIA Population | completed | PHASE3 | 225 |
| NCT01500551 | Long-Term Safety Study Of Tofacitinib In Patients With Juvenile Idiopathic Arthritis | completed | PHASE2/PHASE3 | 302 |
| Sjogren's Syndrome | NCT07281456 | Safety of Tofacitinib, an Oral Janus Kinase Inhibitor, in Primary Sjogren Disease | recruiting | PHASE2 | 60 |
| NCT04496960 | Safety of Tofacitinib, an Oral Janus Kinase Inhibitor, in Primary Sjogren's Syndrome | active not recruiting | PHASE1/PHASE2 | 23 |
| Alopecia Totalis (AT) | NCT07406204 | Tofacitinib vs Methotrexate for Severe Alopecia Areata (TOFA-MTX-AA) | not yet recruiting | PHASE4 | 78 |
| NCT02197455 | Tofacitnib for the Treatment of Alopecia Areata and Variants | completed | PHASE2 | 30 |
| Psoriasis Vulgaris | NCT02193815 | A 12 Day Study To Evaluate A Topical Drug To Treat Plaque Psoriasis | completed | PHASE1 | 15 |
| NCT01831466 | Tofacitinib Ointment For Chronic Plaque Psoriasis | completed | PHASE2 | 476 |
| Dermatomyositis | NCT06438679 | 3T Therapy in the Treatment of MDA5-positive Dermatomyositis | enrolling by invitation | PHASE4 | 133 |
| NCT03002649 | Study of Tofacitinib in Refractory Dermatomyositis | completed | PHASE1 | 10 |
| Granulomatosis With Polyangiitis | NCT04871191 | Study of Salvage Therapy to Treat Patients With Granulomatosis With Polyangiitis | recruiting | PHASE3 | 42 |
| NCT04944524 | Comparison of Tofacitinib and Methotrexate in the Maintained Treatment of GPA | unknown | PHASE4 | 66 |
| Toxic Epidermal Necrolysis | NCT06119490 | Evaluation of the Efficacy and Safety of Methylprednisolone Combined With the JAK Inhibitors in the Treatment of Toxic Epidermal Necrolysis | recruiting | EARLY_PHASE1 | 30 |
| NCT06474078 | Study To Evaluate The Efficacy Of Tofacitinib In Patients With SJS/TEN | completed | NA | 20 |
| Down Syndrome | NCT05662228 | Therapies for Down Syndrome Regression Disorder | active not recruiting | PHASE2 | 66 |
| NCT04246372 | Tofacitinib for Immune Skin Conditions in Down Syndrome | completed | PHASE2 | 47 |
| Vitiligo | NCT07044141 | Efficacy of Oral Tofacitinib in Combination of Narrow Band UVB in Treatment of Vitiligo | active not recruiting | PHASE1 | 20 |
| NCT04246372 | Tofacitinib for Immune Skin Conditions in Down Syndrome | completed | PHASE2 | 47 |
| Atopic Dermatitis (AD) | NCT06923228 | A Study to Assess Efficacy and Safety of CGB-500, 1% Tofacitinib Versus an Active Comparator for Atopic Dermatitis | completed | PHASE2 | 3 |
| NCT06810050 | Phase 2b Safety and Efficacy Study of CGB-500 Topical Ointment With 0.5% and 1% Tofacitnib for Treatment of Atopic Dermatitis | completed | PHASE2 | 180 |
| Depression | NCT04141904 | Tofacitinib in Depression (TIDE) | terminated | PHASE1/PHASE2 | 2 |
| Dermatitis, Atopic | NCT02001181 | Tofacitinib Ointment For Atopic Dermatitis (Atopic Eczema) | completed | PHASE2 | 69 |
| Diaphragm Injury | NCT03681275 | Janus Kinase Inhibition to Prevent Ventilator-induced Diaphragm Dysfunction | recruiting | PHASE2 | 70 |
| Diffuse Large B Cell Lymphoma | NCT05348213 | Novel Targeted Drugs Combined With R-ICE Regimen in Relapsed and Refractory Diffuse Large B-cell Lymphoma | recruiting | PHASE2 | 76 |
| Discoid Lupus Erythematosus | NCT03159936 | Oral Tofacitinib in Adult Subjects With Discoid Lupus Erythematosus (DLE) and Systemic Lupus Erythematosus (SLE) | terminated | EARLY_PHASE1 | 5 |
| Drug Use | NCT04973033 | Effect of Tofacitinib in Treating ANCA-associated Vasculitis | completed | NA | 10 |
| Effect of Drug | NCT04799262 | Tofacitinib as a GC Sparing Agent for Polymyalgia Rheumatica | completed | PHASE2 | 14 |
| Efficacy of Tofacitinib in the Systemic Sclerosis | NCT06044844 | Effectiveness of Tofacitinib in Systemic Sclerosis | unknown | PHASE2 | 44 |
| Epithelioid Mesothelioma | NCT04034238 | Mesothelin-Targeted Immunotoxin LMB-100 in Combination With Tofacitinib in Persons With Previously Treated Pancreatic Adenocarcinoma, Cholangiocarcinoma and Other Mesothelin Expressing Solid Tumors | completed | PHASE1 | 19 |
| Erythematotelangiectatic Rosacea | NCT07343635 | The Efficacy and Safety of Anti-inflammation Treatment (Hirudoid Introduction Followed by Yellow Light Therapy) Combined With Tofacitinib and Doxycycline in Chinese Adult Patients With Mild to Moderate Erythematous Telangiectatic Rosacea | recruiting | NA | 186 |
| Extensive Alopecia Areata | NCT06157905 | Efficacy and Safety of Oral Tofacitinib in the Treatment of Alopecia Areata | completed | EARLY_PHASE1 | 9 |
| Extranodal NK/T-cell Lymphoma | NCT03598959 | Tofacitinib Combined With Chidamide in R/R ENKTCL | unknown | PHASE2 | 20 |
| Frontal Fibrosing Alopecia | NCT06202560 | Effectiveness and Safety of Tofacitinib in Patients With Recalcitrant Frontal Fibrosing Alopecia : A Pilot Study | completed | NA | 11 |
| Glioblastoma | NCT05326464 | Tofacitinib in Recurrent GBM Patients | active not recruiting | PHASE3 | 17 |
| Glucocorticoid Resistant ICIs-related Myocarditis | NCT06393972 | The Efficacy and Safety of Tofacitinib in Patients With Glucocorticoid Resistant ICIs-related Myocarditis | not yet recruiting | PHASE2 | 25 |
| Granuloma Annulare | NCT03910543 | Open-label Trial of Tofacitinib in Cutaneous Sarcoidosis and Granuloma Annulare | completed | PHASE1 | 15 |
| Graves Ophthalmopathy | NCT07547930 | Tofacitinib for Glucocorticoid-Resistant Moderate-to-Severe Thyroid Eye Disease | recruiting | PHASE2 | 8 |
| Graves Orbitopathy | NCT07547930 | Tofacitinib for Glucocorticoid-Resistant Moderate-to-Severe Thyroid Eye Disease | recruiting | PHASE2 | 8 |
| Healthy Subjects | NCT04468425 | Tofacitinib Citrate Topical Gel 3.2% FDA BA Bridging Study | completed | PHASE1 | 14 |
| Idiopathic Inflammatory Myopathies | NCT05400889 | Clinical Characteristics and Mechanism Research of Inhibitors of Janus Kinase in the Idiopathic Inflammatory Myopathies | unknown | PHASE2 | 10 |
| IgG4-related Disease | NCT05625581 | Tofatib Treatment for IgG4-related Disease | unknown | N/A | 40 |
| ILD | NCT04311567 | Effects of Tofacitinib vs Methotrexate on Rheumatoid Arthritis Interstitial Lung Disease | terminated | PHASE4 | 3 |
| Ileal Pouch | NCT04580277 | Tofacitinib For Treatment Of Chronic Pouchitis | terminated | PHASE2 | 6 |
| Ileal Pouchitis | NCT04580277 | Tofacitinib For Treatment Of Chronic Pouchitis | terminated | PHASE2 | 6 |
| Immune-Mediated Colitis | NCT04768504 | Tofacitinib for the Treatment of Refractory Immune-related Colitis from Checkpoint Inhibitor Therapy- TRICK Study | terminated | PHASE2 | 2 |
| Immunomodulation | NCT01736696 | Multiple Dose Escalation Study In Medically Stable Subjects With Psoriasis | completed | PHASE1 | 59 |
| Inflamatory Bowel Disease | NCT07487311 | A Prospective Cohort Study Evaluating the Efficacy and Safety of Guselkumab (GUS) With JAK Inhibitors in Patients With Difficult-To-Treat Inflammatory Bowel Disease (IBD) | recruiting | N/A | 80 |
| Inflammation | NCT04141904 | Tofacitinib in Depression (TIDE) | terminated | PHASE1/PHASE2 | 2 |
| Inflammatory Bowel Diseases | NCT03885713 | Identification of Predictive Biomarkers for Response to Biologic Therapies and Tofacitinib in Inflammatory Bowel Disease | completed | PHASE4 | 180 |
| Inflammatory Gastrointestinal Disease | NCT05104723 | Safety and Efficacy of Tofacitinib for Chronic Granulomatous Disease With Inflammatory Complications | completed | PHASE1/PHASE2 | 10 |
| Inflammatory Lung Disease | NCT05104723 | Safety and Efficacy of Tofacitinib for Chronic Granulomatous Disease With Inflammatory Complications | completed | PHASE1/PHASE2 | 10 |
| Inflammatory Skin Disease | NCT05104723 | Safety and Efficacy of Tofacitinib for Chronic Granulomatous Disease With Inflammatory Complications | completed | PHASE1/PHASE2 | 10 |
| Inhibition | NCT04299971 | Efficiency of Methotrexate and Tofacitinib in Mild and Moderate Patients | unknown | PHASE4 | 130 |
| Interstitial Lung Disease | NCT05246293 | Tofacitinib in the Treatment of Rheumatoid Arthritis-related Interstitial Lung Disease. | unknown | PHASE2 | 60 |
| Interstitial Lung Disease Due to Systemic Disease (Disorder) | NCT04311567 | Effects of Tofacitinib vs Methotrexate on Rheumatoid Arthritis Interstitial Lung Disease | terminated | PHASE4 | 3 |
| Itch | NCT06201715 | Efficacy and Safety of Tofacitinib in Patients With Prurigo Nodularis | unknown | NA | 24 |
| JAK-STAT Pathway Deregulation | NCT04973033 | Effect of Tofacitinib in Treating ANCA-associated Vasculitis | completed | NA | 10 |
| Janus Kinase Inhibitors | NCT06573593 | Efficacy and Safety of JAK Inhibitors in Patients With AA: RWE Study | recruiting | N/A | 150 |
| Juvenile Idiopathic Arthritis (JIA) | NCT07211932 | Tofacitinib in Juvenile Idiopathic Arthritis | not yet recruiting | N/A | 58 |
| Kidney Transplantation | NCT01375127 | Collection of Follow-up Data From CP-690,550-treated Kidney Transplant Recipients | completed | N/A | 83 |
| LAL | NCT07522801 | A Precision Medicine Trial for Patients With Relapsed or Refractory T Cell ALL | not yet recruiting | PHASE2 | 93 |
| Lichen Planopilaris of Scalp | NCT06202560 | Effectiveness and Safety of Tofacitinib in Patients With Recalcitrant Frontal Fibrosing Alopecia : A Pilot Study | completed | NA | 11 |
| Major Adverse Cardiac Events | NCT07554820 | Major Adverse Cardiovascular Events (MACE) in Rheumatoid Arthritis Patient With Moderate to Severe Disease Activity Treated With Tofacitinib and Statins vs TNF Inhibitors: TOFSTAT CLINICAL TRIAL | recruiting | PHASE4 | 120 |
| Methotrexate | NCT04299971 | Efficiency of Methotrexate and Tofacitinib in Mild and Moderate Patients | unknown | PHASE4 | 130 |
| Moderate to Severe Rheumatoid Arthritis | NCT07008846 | Efficacy of Tofacitinib, Methotrexate Combination Therapy Versus Upadacitinib, Methotrexate Combination Therapy in Moderate to Severe Rheumatoid Arthritis | active not recruiting | PHASE3 | 96 |
| Myasthenia Gravis, Generalized | NCT04431895 | Safety And Efficacy Of Tofacitinib In Patients With Refractory Myasthenia Gravis: A Pilot Study | completed | EARLY_PHASE1 | 19 |
| Nail Psoriasis | NCT07313072 | Topical Use of 2% Tofacitinib for Nail Psoriasis: an Exploratory Clinical Study | not yet recruiting | PHASE2 | 10 |
| Neoplasms With Mesothelin Expression | NCT04034238 | Mesothelin-Targeted Immunotoxin LMB-100 in Combination With Tofacitinib in Persons With Previously Treated Pancreatic Adenocarcinoma, Cholangiocarcinoma and Other Mesothelin Expressing Solid Tumors | completed | PHASE1 | 19 |
| Oral Lichen Planus | NCT07131813 | Evaluation of Efficacy and Safety of add-on Tofacitinib in Patients With Oral Lichen Planus | recruiting | PHASE4 | 60 |
| Palmoplantar Pustulosis (PPP) | NCT07530367 | A Phase III Randomized Controlled Trial Evaluating the Efficacy and Safety of Tofacitinib Combined With Imatinib in Patients With Moderate-to-Severe Palmoplantar Pustulosis | not yet recruiting | PHASE3 | 135 |
| Plaque Psoriasis | NCT01710046 | Study Of The Mechanism Of Action Of CP-690,550 In The Skin Of Subjects With Moderate To Severe Chronic Plaque Psoriasis | completed | PHASE2 | 12 |
| Pneumonitis, Interstitial | NCT04390061 | TOFAcitinib Plus Hydroxycloroquine vs Hydroxycloroquine in Patients With COVID-19 Interstitial Pneumonia | unknown | PHASE2 | 116 |
| Polyarticular Course Juvenile Idiopathic Arthritis (JIA) | NCT06654882 | Trial of Sequential Medications AfteR TNFi Failure in Juvenile Idiopathic Arthritis | recruiting | PHASE3 | 400 |
| Pouchitis | NCT04580277 | Tofacitinib For Treatment Of Chronic Pouchitis | terminated | PHASE2 | 6 |
| Primary Cutaneous Amyloidosis | NCT06998875 | A Prospective Cohort Study on Primary Cutaneous Amyloidosis | recruiting | PHASE4 | 56 |
| Primary Sjögren's Syndrome | NCT05087589 | Efficacy, Safety and Immunological Evaluation of Tofacitinib in the Treatment of Primary Sjogren's Syndrome | unknown | PHASE2 | 10 |
| Prurigo Nodularis | NCT06201715 | Efficacy and Safety of Tofacitinib in Patients With Prurigo Nodularis | unknown | NA | 24 |
| RA | NCT04311567 | Effects of Tofacitinib vs Methotrexate on Rheumatoid Arthritis Interstitial Lung Disease | terminated | PHASE4 | 3 |
| Reduction | NCT04610476 | Impact of Tapering Immunosuppressants on Maintaining Minimal Disease Activity in Adult Subjects With Psoriatic Arthritis | unknown | PHASE3 | 270 |
| Regression | NCT05662228 | Therapies for Down Syndrome Regression Disorder | active not recruiting | PHASE2 | 66 |
| Rhematoid Arthritis | NCT02187055 | An Efficacy And Safety Study Evaluating Tofacitinib With And Without Methotrexate Compared To Adalimumab With Methotrexate | completed | PHASE4 | 1,152 |
| Rheumatic Arthritis | NCT04485325 | Capability of Tofacitinib or Etanercept to Accelerate Tapering of NSAID and Treat-to-target Guided De-escalation of Corticosteroids in RA Patients | completed | PHASE4 | 92 |
| Rheumatic Disease | NCT07138898 | Immunosuppressant Management in Rheumatology Patients Undergoing Elective Total Shoulder Arthroplasty | not yet recruiting | PHASE2 | 80 |
| Rheumatoid Arthritis (RA | NCT06945666 | A Study of Iguratimod in Combination With Tofacitinib in RA Patients | not yet recruiting | PHASE4 | 200 |
| Rhumatoid Arthisis | NCT06687551 | JAK Inhibitor Dose TAPering Strategy Study | not yet recruiting | PHASE4 | 308 |
| Sacroilitis | NCT04062695 | Tofacitinib for Reduction of Spinal Inflammation in Patients With Psoriatic ArthritiS PresenTing With Axial InvOlvement | unknown | PHASE2 | 80 |
| Safety Issues | NCT04799262 | Tofacitinib as a GC Sparing Agent for Polymyalgia Rheumatica | completed | PHASE2 | 14 |
| Sarcoidosis | NCT03793439 | Tofacitinib Hypothesis-generating, Pilot Study for Corticosteroid-Dependent Sarcoidosis | completed | PHASE1 | 5 |
| Sarcoidosis Lung | NCT03793439 | Tofacitinib Hypothesis-generating, Pilot Study for Corticosteroid-Dependent Sarcoidosis | completed | PHASE1 | 5 |
| Sarcoidosis, Pulmonary | NCT03793439 | Tofacitinib Hypothesis-generating, Pilot Study for Corticosteroid-Dependent Sarcoidosis | completed | PHASE1 | 5 |
| SARS-COv2 Related Interstitial Pneumonia | NCT04332042 | TOFAcitinib in SARS-CoV2 Pneumonia | unknown | PHASE2 | 50 |
| Scleritis | NCT03580343 | Tofacitinib for Inflammatory Eye Disease | unknown | PHASE2 | 5 |
| Scleroderma | NCT03274076 | Evaluation of Tofacitinib in Early Diffuse Cutaneous Systemic Sclerosis (dcSSc) | completed | PHASE1/PHASE2 | 15 |
| Scleroderma, Systemic | NCT07472166 | Efficacy of Tofacitinib on Skin Thickening in Diffuse Cutaneous Systemic Sclerosis: A Comparative Study With Methotrexate | completed | PHASE4 | 34 |
| Spondylarthritis | NCT05080218 | COVID-19 VaccinE Response in Rheumatology Patients | completed | PHASE4 | 841 |
| Spondylitis | NCT04062695 | Tofacitinib for Reduction of Spinal Inflammation in Patients With Psoriatic ArthritiS PresenTing With Axial InvOlvement | unknown | PHASE2 | 80 |
| Spondyloarthritis | NCT03504072 | Risk of Tuberculous and Other Infections in Patients of Spondyloarthritis Treated With Tofacitinib in Bangladesh | unknown | PHASE4 | 174 |
| Spondyloarthritis, Axial | NCT06114407 | Baricitinib in the Treatment of Refractory Axial Spondyloarthritis Patients: A Comparison With Tofacitinib | unknown | PHASE2 | 184 |
| Spondyloarthropathy | NCT05431283 | Real-world Effectiveness of Tofacitinib on Ulcerative Colitis Associated Spondyloarthropathy | unknown | N/A | 100 |
| Stevens-Johnson Syndrome | NCT06474078 | Study To Evaluate The Efficacy Of Tofacitinib In Patients With SJS/TEN | completed | NA | 20 |
| Systemic Sclerosis | NCT03274076 | Evaluation of Tofacitinib in Early Diffuse Cutaneous Systemic Sclerosis (dcSSc) | completed | PHASE1/PHASE2 | 15 |
| Telitacicept | NCT06979271 | Efficacy and Safety of Telitacicept Combined With Tofacitinib for Refractory Rheumatoid Arthritis | recruiting | N/A | 20 |
| Thromboembolism | NCT05313620 | Effect of Tofacitinib on Coagulation and Platelet Function, and Its Role in Thromboembolic Events | recruiting | PHASE4 | 30 |
| Thyroid Eye Disease, TED | NCT07547930 | Tofacitinib for Glucocorticoid-Resistant Moderate-to-Severe Thyroid Eye Disease | recruiting | PHASE2 | 8 |
| Treatment | NCT04299971 | Efficiency of Methotrexate and Tofacitinib in Mild and Moderate Patients | unknown | PHASE4 | 130 |
| Treatment Compliance | NCT06979271 | Efficacy and Safety of Telitacicept Combined With Tofacitinib for Refractory Rheumatoid Arthritis | recruiting | N/A | 20 |
| Ulcerative Colitis Acute | NCT04925973 | Tofacitinib for Hospitalized Acute Severe Ulcerative Colitis Management | active not recruiting | PHASE2 | 24 |
| Uveitis | NCT03580343 | Tofacitinib for Inflammatory Eye Disease | unknown | PHASE2 | 5 |
| Vitiligo, Generalized | NCT07055529 | Comparison of Efficacy and Safety Psoralen Combined With Ultraviolet A (PUVA) Vs Tofacitinib in the Treatment of Generalized Vitiligo. | not yet recruiting | EARLY_PHASE1 | 64 |
| Withdrawal | NCT04610476 | Impact of Tapering Immunosuppressants on Maintaining Minimal Disease Activity in Adult Subjects With Psoriatic Arthritis | unknown | PHASE3 | 270 |
| Active Mild Ulcerative Colitis, Active Moderate Ulcerative Colitis, Healthy Subjects | NCT03103412 | TD-3504 SAD in Healthy Subjects and Subjects With Ulcerative Colitis (UC) | completed | PHASE1 | 32 |
| Active Moderate to Severe Rheumatoid Arthritis | NCT04876781 | Korean Post-marketing Surveillance for Xeljanz XR | recruiting | N/A | 200 |
| Active Psoriatic Arthritis | NCT04876781 | Korean Post-marketing Surveillance for Xeljanz XR | recruiting | N/A | 200 |
| Acute Severe Ulcerative Colitis | NCT07297069 | Combination Therapy With Infliximab and Tofacitinib for Acute Severe Ulcerative Colitis - CINTO Trial | not yet recruiting | PHASE2 | 60 |
| Adenocarcinoma, Pancreatic | NCT04034238 | Mesothelin-Targeted Immunotoxin LMB-100 in Combination With Tofacitinib in Persons With Previously Treated Pancreatic Adenocarcinoma, Cholangiocarcinoma and Other Mesothelin Expressing Solid Tumors | completed | PHASE1 | 19 |
| Alopecia Areata (AA) | NCT02197455 | Tofacitnib for the Treatment of Alopecia Areata and Variants | completed | PHASE2 | 30 |
| Alopecia Areata(AA) | NCT07101471 | Rhofanib® (Tofacitinib) Safety and Effectiveness Evaluation | completed | N/A | 296 |
| Alopecia Totalis/Universalis | NCT07101471 | Rhofanib® (Tofacitinib) Safety and Effectiveness Evaluation | completed | N/A | 296 |
| Alopecia Universalis (AU) | NCT02197455 | Tofacitnib for the Treatment of Alopecia Areata and Variants | completed | PHASE2 | 30 |
| Amyotrophic Lateral Sclerosis | NCT06689982 | Tofacitinib in Patients With Amyotrophic Lateral Sclerosis | not yet recruiting | EARLY_PHASE1 | 12 |
| ANCA Associated Vasculitis | NCT04973033 | Effect of Tofacitinib in Treating ANCA-associated Vasculitis | completed | NA | 10 |
| Aneurysm | NCT05845723 | Tocilizumab and Tofacitinib in the Treatment of Vascular Behçet's Syndrome | recruiting | PHASE2 | 81 |
| Anti-neutrophil Cytoplasmic Antibody-associated Vasculitis | NCT04871191 | Study of Salvage Therapy to Treat Patients With Granulomatosis With Polyangiitis | recruiting | PHASE3 | 42 |
| Arthritis Juvenile Idiopathic | NCT03000439 | A Safety, Efficacy And Pharmacokinetics Study Of Tofacitinib In Pediatric Patients With sJIA | completed | PHASE3 | 100 |
| Arthritis Rheumatoid | NCT04721821 | Comparative Effectiveness Of Tumor Necrosis Factor Inhibitors And Tofacitinib Use In Earlier Lines Of Therapy And Use As Monotherapy. | completed | N/A | 7,807 |
| Arthritis, Psoriatic | NCT01976364 | Open-Label Extension Study Of Tofacitinib In Psoriatic Arthritis | completed | PHASE3 | 686 |
| Atopic Dermatitis / Eczema | NCT04246372 | Tofacitinib for Immune Skin Conditions in Down Syndrome | completed | PHASE2 | 47 |
| Behcet Syndrome, Vascular Type | NCT05845723 | Tocilizumab and Tofacitinib in the Treatment of Vascular Behçet's Syndrome | recruiting | PHASE2 | 81 |
| Blau Syndrome | NCT06688838 | Effective Treatment of Jak1/3 Inhibitor in Blau Syndrome | enrolling by invitation | N/A | 24 |
| Cholangiocarcinoma, Extrahepatic | NCT04034238 | Mesothelin-Targeted Immunotoxin LMB-100 in Combination With Tofacitinib in Persons With Previously Treated Pancreatic Adenocarcinoma, Cholangiocarcinoma and Other Mesothelin Expressing Solid Tumors | completed | PHASE1 | 19 |
| Chronic Granulomatous Disease | NCT05104723 | Safety and Efficacy of Tofacitinib for Chronic Granulomatous Disease With Inflammatory Complications | completed | PHASE1/PHASE2 | 10 |
| Clinically Amyopathic Dermatomyisitis(CAMD) | NCT04613219 | Correlation Between the Change of Peripheral Lymphocyte Subsets and Clinically Amyopathic Dermatomyositis Combined With Rapidly Progressive Interstitial Lung Disease | unknown | N/A | 80 |
| COVID-19 Pneumonia | NCT04415151 | Tofacitinib for Treatment of Moderate COVID-19 | terminated | PHASE2 | 24 |
| Covid19 | NCT04469114 | Tofacitinib in Hospitalized Patients With COVID-19 Pneumonia | completed | PHASE3 | 289 |
| Crohn Disease | NCT03885713 | Identification of Predictive Biomarkers for Response to Biologic Therapies and Tofacitinib in Inflammatory Bowel Disease | completed | PHASE4 | 180 |
| Cutaneous Leishmaniasis, American | NCT06011343 | Tofacitinib Associated With Meglumine Antimoniate in Cutaneous Leishmaniasis | unknown | PHASE2/PHASE3 | 22 |
| Cutaneous Sarcoidosis | NCT03910543 | Open-label Trial of Tofacitinib in Cutaneous Sarcoidosis and Granuloma Annulare | completed | PHASE1 | 15 |
| Cutaneous T-Cell Lymphoma | NCT06698822 | A Phase 2 Trial to Assess Safety and Efficacy of Tofacitinib 2% Cream in the Treatment of Cutaneous T-cell Lymphoma (CTCL), Stages IA, IB, and IIA | recruiting | PHASE2 | 20 |