Effectiveness and Safety of Tofacitinib in Patients With Extensive and Recalcitrant Alopecia Areata |
Active, not recruiting |
Alopecia Areata |
NCT03800979 |
Study of Tofacitinib in Refractory Dermatomyositis |
Active, not recruiting |
Dermatomyositis |
NCT03002649 |
IDentification of Factors Predictive of Tofacitinib's Survival in Patient With Rheumatoid Arthritis |
Recruiting |
Arthritis, Rheumatoid |
NCT03981900 |
Efficiency of Methotrexate and Tofacitinib in Mild and Moderate Patients |
Recruiting |
Takayasu Arteritis|Methotrexate|Inhibition|Treatment |
NCT04299971 |
Tofacitinib for Immune Skin Conditions in Down Syndrome |
Not yet recruiting |
Down Syndrome|Alopecia|Atopic Dermatitis/Eczema|Hidradenitis Suppurativa|Vitiligo|Psoriasis |
NCT04246372 |
A Study to Demonstrate the Equivalence of the Tofacitinib Oral Solution to the Tablet Formulation in Healthy Participants. |
Completed |
Healthy |
NCT04111614 |
Tofacitinib in Depression (TIDE) |
Recruiting |
Depression|Inflammation |
NCT04141904 |
Effects of Tofacitinib vs Methotrexate on Rheumatoid Arthritis Interstitial Lung Disease |
Not yet recruiting |
Rheumatoid Arthritis|Interstitial Lung Disease Due to Systemic Disease (Disorder) |
NCT04311567 |
Safety and Efficacy of Tofacitinib vs Methotrexate in the Treatment of Psoriatic Arthritis |
Completed |
Psoriatic Arthritis |
NCT03736161 |
Tofacitinib for Inflammatory Eye Disease |
Active, not recruiting |
Uveitis|Scleritis |
NCT03580343 |
Tofacitinib for the Treatment of Alopecia Areata and Its Variants |
Completed |
Alopecia Areata|Alopecia Totalis|Alopecia Universalis |
NCT02312882 |
Risk of Tuberculous and Other Infections in Patients of Spondyloarthritis Treated With Tofacitinib in Bangladesh |
Recruiting |
Spondyloarthritis |
NCT03504072 |
Effectiveness and Safety of Tofacitinib in Korean Patients With Rheumatoid Arthritis |
Recruiting |
Rheumatoid Arthritis |
NCT03011281 |
Open-label Trial of Tofacitinib in Cutaneous Sarcoidosis and Granuloma Annulare |
Recruiting |
Cutaneous Sarcoidosis|Granuloma Annulare |
NCT03910543 |
Evaluation of Tofacitinib in Early Diffuse Cutaneous Systemic Sclerosis (dcSSc) |
Completed |
Systemic Sclerosis|Scleroderma |
NCT03274076 |
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 |
Rheumatoid Arthritis |
NCT02281552 |
Study to Evaluate the Bioequivalence of Pfizer Korea Inc. "XELJANZ 5Mg Tablet" in Healthy Volunteers |
Completed |
Rheumatoid Arthritis |
NCT03868072 |
Open-label Study of Tofacitinib for Moderate to Severe Skin Involvement in Young Adults With Lupus |
Recruiting |
Cutaneous Lupus|Systemic Lupus Erythematosus |
NCT03288324 |
Efficacy Study Of Tofacitinib In Pediatric JIA Population |
Completed |
Juvenile Idiopathic Arthritis |
NCT02592434 |
Study To Evaluate The Efficacy Of Tofacitinib In Moderate To Severe Alopecia Areata, Totalis And Universalis |
Completed |
Alopecia Areata |
NCT02299297 |
Topical Tofacitinib for the Treatment of Alopecia Areata and Its Variants |
Completed |
Alopecia Areata|Alopecia Totalis|Alopecia Universalis |
NCT02812342 |
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 |
Rheumatoid Arthritis |
NCT02566967 |
Effects of Tofacitinib on Body Composition, Bone Mineral Density and Bone Marrow Adiposity in Patients With Rheumatoid Arthritis: the TOFAT Project |
Not yet recruiting |
Rheumatoid Arthritis |
NCT04175886 |
Tofacitinib Response in Ulcerative Colitis - a Real World Prospective Multi-center Study |
Enrolling by invitation |
Ulcerative Colitis |
NCT03772145 |
Oral Tofacitinib in Adult Subjects With Discoid Lupus Erythematosus (DLE) and Systemic Lupus Erythematosus (SLE) |
Recruiting |
Discoid Lupus Erythematosus|Systemic Lupus Erythematosus |
NCT03159936 |
Safety of Tofacitinib, an Oral Janus Kinase Inhibitor, in Systemic Lupus Erythematosus |
Completed |
Systemic Lupus Erythematosus |
NCT02535689 |
Tofacitinib for Reduction of Spinal Inflammation in Patients With Psoriatic ArthritiS PresenTing With Axial InvOlvement |
Not yet recruiting |
Psoriatic Arthritis|Spondylitis|Sacroilitis |
NCT04062695 |
A Study To Evaluate The Effect Of Food On The Behavior of Tofacitinib Modified Release 22 Milligram Tablets In Healthy Volunteers |
Completed |
Healthy |
NCT02487433 |
Observational Study to Determine How Physicians Make Treatment Decisions in Patients Treated With Tofacitinib for Moderate to Severe Active Rheumatoid Arthritis |
Recruiting |
Arthritis, Rheumatoid |
NCT03387423 |
Safety and Efficacy of Tofacitinib in the Treatment of NSAID Refractory Axial Spondyloarthritis:A Clinical Trial |
Recruiting |
Axial Spondyloarthritis |
NCT03738956 |
Musculoskeletal Ultrasound Assessment of Therapeutic Response of Tofacitinib in Rheumatoid Arthritis Patients |
Completed |
Rheumatoid Arthritis |
NCT02321930 |
Efficacy And Safety Of Tofacitinib In Chinese Subjects With Active Psoriatic Arthritis |
Recruiting |
Psoriatic Arthritis |
NCT03486457 |
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 |
Healthy |
NCT02084875 |
A Safety, Efficacy And Pharmacokinetics Study Of Tofacitinib In Pediatric Patients With sJIA |
Recruiting |
Arthritis Juvenile Idiopathic |
NCT03000439 |
Long-Term Safety Study Of Tofacinib In Patients With Juvenile Idiopathic Arthritis |
Recruiting |
Juvenile Idiopathic Arthritis |
NCT01500551 |
Mesothelin-Targeted Immunotoxin LMB-100 in Combination With Tofacitinib in Persons With Previously Treated Pancreatic Adenocarcinoma, Cholangiocarcinoma and Other Mesothelin Expressing Solid Tumors |
Recruiting |
Neoplasms With Mesothelin Expression|Epithelioid Mesothelioma|Cholangiocarcinoma, Extrahepatic|Adenocarcinoma, Pancreatic |
NCT04034238 |
Methotrexate Withdrawal Study of Tofacitinib Modified Release Formulation in Subjects With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT02831855 |
Study to Evaluate HL-TOF Tab. 5 mg Compared With XelJanz Tab. in Healthy Volunteers |
Recruiting |
Healthy Volunteers |
NCT04114461 |
Efficacy and Safety of Tofacitinib in Subjects With Active Ankylosing Spondylitis (AS) |
Active, not recruiting |
Ankylosing Spondylitis |
NCT03502616 |
A Study to Assess Immune Response Following Zoster Vaccination to Subjects With Rheumatoid Arthritis Receiving Tofacitinib or Placebo With Background Methotrexate |
Completed |
Rheumatoid Arthritis |
NCT02147587 |
A Phase 1 Study To Evaluate The Pharmacokinetics (PK), Safety, And Bioavailability Of A Modified-Release (MR) Formulation Of Tofacitinib In Healthy Volunteers |
Completed |
Healthy |
NCT01731327 |
Tofacitinib Hypothesis-generating, Pilot Study for Corticosteroid-Dependent Sarcoidosis |
Recruiting |
Sarcoidosis, Pulmonary|Sarcoidosis Lung|Sarcoidosis |
NCT03793439 |
Tofacitinib Combined With Chidamide in R/R ENKTCL |
Not yet recruiting |
Extranodal NK/T-cell Lymphoma |
NCT03598959 |
Open-Label Extension Study Of Tofacitinib In Psoriatic Arthritis |
Completed |
Arthritis, Psoriatic |
NCT01976364 |
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 |
Healthy |
NCT01499004 |
An Efficacy And Safety Study Evaluating Tofacitinib With And Without Methotrexate Compared To Adalimumab With Methotrexate |
Completed |
Rhematoid Arthritis |
NCT02187055 |
Effects of Tofacitinib (CP-690,550) on Magnetic Resonance Imaging (MRI)- Assessed Joint Structure In Early Rheumatoid Arthritis (RA) |
Completed |
Rheumatoid Arthritis |
NCT01164579 |
Tofacitinib Ointment For Atopic Dermatitis (Atopic Eczema) |
Completed |
Dermatitis, Atopic |
NCT02001181 |
Tofacitinib Bioequivalence Study Comparing Tablets And Capsules |
Completed |
Healthy |
NCT01599377 |
Dose-Ranging Study Of Tofacitinib In Adults With Active Ankylosing Spondylitis |
Completed |
Ankylosing Spondylitis |
NCT01786668 |
Effect Of Ketoconazole On The Pharmacokinetics Of Tasocitinib (CP-690,550) In Healthy Volunteers |
Completed |
Healthy |
NCT01202240 |
Tofacitinib (Xeljanz) Special Investigation for Rheumatoid Arthritis |
Active, not recruiting |
Rheumatoid Arthritis |
NCT01932372 |
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) |
Recruiting |
Arthritis, Rheumatoid |
NCT03970837 |
Tofacitinib In Psoriatic Arthritis Subjects With Inadequate Response to TNF Inhibitors |
Completed |
Psoriatic Arthritis |
NCT01882439 |
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 |
Recruiting |
Arthritis, Rheumatoid |
NCT03980483 |
JAK Inhibition to Prevent Ventilator-induced Diaphragm Dysfunction |
Recruiting |
Diaphragm Injury |
NCT03681275 |
Tofacitinib Registry of Patients With Ulcerative Colitis in Germany |
Recruiting |
Colitis, Ulcerative|Biologics|Tofacitiniib|Chronic Inflammatory Small Bowel Disease|Bowel Diseases, Inflammatory|Bowel Disease|CED |
NCT04032756 |
Tofacitinib Ointment For Chronic Plaque Psoriasis |
Completed |
Psoriasis Vulgaris|Psoriasis |
NCT01831466 |
Identify Predictors That Distinguish Between Tofacitinib Responders and Non-responders Based on Genotype and Cellular and Molecular Profiles From Pinch Biopsies, Blood and Stool Samples |
Recruiting |
Ulcerative Colitis |
NCT03663400 |
Tofacitnib for the Treatment of Alopecia Areata and Variants |
Completed |
Alopecia Areata (AA)|Alopecia Totalis (AT)|Alopecia Universalis (AU) |
NCT02197455 |
Shingrix Vaccine in Patients With Moderate to Severe Ulcerative Colitis on Tofacitinib |
Recruiting |
Inflammatory Bowel Diseases |
NCT03591770 |
A Study To Compare The Effectiveness Of Tofacitinib 11 Mg Once A Day To Tofacitinib 5 Mg Twice A Day |
Completed |
Arthritis Rheumatoid |
NCT04267380 |
Comparative Analysis of Outcomes Among Patients Treated With Xeljanz vs Biologics |
Active, not recruiting |
Arthritis, Rheumatoid |
NCT03964649 |
Evaluation of Pain Sensitization in Rheumatoid Arthritis: Analysis on a Cohort of Tofacitinib Treated Patients |
Recruiting |
Rheumatoid Arthritis |
NCT03815578 |
Safety Study Of Tofacitinib Versus Tumor Necrosis Factor (TNF) Inhibitor In Subjects With Rheumatoid Arthritis |
Active, not recruiting |
Arthritis, Rheumatoid |
NCT02092467 |
Efficacy And Safety Of Tofacitinib In Psoriatic Arthritis: Comparator Study |
Completed |
Psoriatic Arthritis |
NCT01877668 |
PK Study in Adult Healthy Volunteers to Assess QD Dosing With the Selected Age-appropriate MR Formulations |
Completed |
Healthy |
NCT03112148 |
Examination of Efficacy and Safety of Baricitinib in RA Patients |
Recruiting |
Rheumatoid Arthritis |
NCT03755466 |
Collection of Follow-up Data From CP-690,550-treated Kidney Transplant Recipients |
Completed |
Kidney Transplantation |
NCT01375127 |
Changes of Depression After First-year of Tofacitinib in RA Patients |
Not yet recruiting |
Rheumatoid Arthritis |
NCT03992781 |
Predictors of Response to Tofacitinib Treatment in Rheumatoid Arthritis Patients |
Not yet recruiting |
Rheumatoid Arthritis |
NCT04079920 |
Comparative Analysis of Outcomes Among Patients Initiating Xeljanz in Combination With Oral MTX Who Withdraw MTX Versus Continue MTX |
Completed |
Rheumatoid Arthritis |
NCT03975790 |
A Study Of Tasocitinib In Dry Eye Subjects |
Withdrawn |
Keratoconjunctivitis Sicca |
NCT01226680 |
Comparative Analysis of Adherence and Effectiveness Outcomes Between Rheumatoid Arthritis (RA) Patients Treated With Tofacitinib Modified Release (MR) |
Completed |
Rheumatoid Arthritis |
NCT04018001 |
Patient-Reported Outcomes In Rheumatoid Arthritis Patients Treated With Tofacitinib Or Biological Disease-Modifying Antirheumatic Drugs (DMARDs) In Real Life Conditions |
Completed |
Arthritis, Rheumatoid |
NCT03073109 |
A Study To Evaluate The Effect Of Food On How Tasocitinib (CP-690,550) Is Absorbed And Moves Through The Body Following Oral Administration Of Tasocitinib (CP-690,550) Tablets To Healthy Subjects |
Completed |
Rheumatoid Arthritis |
NCT01184001 |
Effects Of CP-690,550 (Tasocitinib) On Cholesterol Metabolism In Patients With Active Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT01262118 |
Safety and Efficacy of Pf-06650833 In Subjects With Rheumatoid Arthritis, With An Inadequate Response To Methotrexate |
Completed |
Rheumatoid Arthritis |
NCT02996500 |
A Study To Compare The Amount Of Tasocitinib (CP-690,550) That Is Absorbed Into The Blood Of Healthy Subjects Following Oral Administration Of Three Different Tablet Versions Of Tasocitinib (CP-690,550) |
Completed |
Rheumatoid Arthritis |
NCT01184092 |
TD-3504 SAD in Healthy Subjects and Subjects With Ulcerative Colitis (UC) |
Completed |
Active Mild Ulcerative Colitis, Active Moderate Ulcerative Colitis, Healthy Subjects |
NCT03103412 |
Rheumatoid Arthritis Satisfaction Outcome Research |
Recruiting |
Rheumatoid Arthritis |
NCT03703817 |
Estimate The Effect Of Repeat-Dose Rifampin On The Pharmacokinetics Of CP-690,550 In Healthy Volunteers |
Completed |
Healthy |
NCT01204112 |
Korea Post-marketing Surveillance for Xeljanz (Registered) in Ulcerative Colitis Patients |
Not yet recruiting |
Ulcerative Colitis |
NCT04071405 |
Evaluation of the Condition of Rheumatoid Arthritis After Treatment |
Recruiting |
Rheumatoid Arthritis |
NCT02157012 |
Advanced Therapeutics in Rheumatoid Arthritis (RA) |
Recruiting |
Rheumatoid Arthritis |
NCT03976245 |
A Study of Tofacitinib in Patients With Ulcerative Colitis in Stable Remission |
Active, not recruiting |
Ulcerative Colitis |
NCT03281304 |
A Study Evaluating The Efficacy And Safety Of CP-690,550 In Patients With Moderate To Severe Ulcerative Colitis |
Completed |
Ulcerative Colitis |
NCT01465763 |
A Study To Evaluate Both The Efficacy and Safety Profile of CP-690,550 In Patients With Moderately to Severely Active Ulcerative Colitis |
Completed |
Ulcerative Colitis |
NCT01458951 |
A Study To Estimate The Amount Of CP-690,550 (Study Drug) That Is Absorbed Into The Blood Of Healthy Subjects Following Oral Administration Of CP-690,550 In Tablet Form |
Completed |
Healthy |
NCT01143805 |
Xeljanz Special Investigation for Long-term Use in UC Patients |
Active, not recruiting |
Ulcerative Colitis |
NCT03643211 |
Korean Post-marketing Surveillance for Xeljanz |
Recruiting |
Rheumatoid Arthritis|Psoriatic Arthritis |
NCT02984020 |
Safety and Tolerability of Herpes Zoster Vaccine Rheumatologic Patients |
Active, not recruiting |
Herpes Zoster |
NCT03016884 |
Pharmacokinetics Of CP-690,550 In Pediatric Patients With Juvenile Idiopathic Arthritis (JIA) |
Completed |
Juvenile Idiopathic Arthritis |
NCT01513902 |
Long-Term Effectiveness And Safety Of CP-690,550 For The Treatment Of Rheumatoid Arthritis |
Completed |
Arthritis, Rheumatoid |
NCT00413699 |
Senica |
MUDr. Pavol Polak s.r.o. |
Slovakia|Hospital Nuestra Senora de la Esperanza |
Nestatne zdravotnicke zariadenie |
Co-Administration Of Methotrexate And CP-690,550 |
Completed |
Rheumatoid Arthritis |
NCT01745055 |
A Study to Evaluate Patient Characteristics and Treatment Patterns Among Rheumatoid Arthritis Patients |
Completed |
Rheumatoid Arthritis |
NCT04047121 |
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 |
Rheumatoid Arthritis |
NCT01741493 |
A 12 Day Study To Evaluate A Topical Drug To Treat Plaque Psoriasis |
Completed |
Psoriasis Vulgaris |
NCT02193815 |
Study Of The Mechanism Of Action Of CP-690,550 In The Skin Of Subjects With Moderate To Severe Chronic Plaque Psoriasis |
Completed |
Plaque Psoriasis |
NCT01710046 |
A Study To Evaluate The Effect Of CP-690,550 On Measures Of Kidney Function In Patients With Active Rheumatoid Arthritis |
Completed |
Arthritis, Rheumatoid |
NCT01484561 |
The Safety And Efficacy Of Maintenance Therapy With CP-690,550 |
Completed |
Crohn's Disease |
NCT01393899 |
Effects of Antirheumatic Treatment on Levels of Survivin in Rheumatoid Arthritis Patients |
Recruiting |
Rheumatoid Arthritis |
NCT03440892 |
Multiple Dose Escalation Study In Medically Stable Subjects With Psoriasis |
Completed |
Psoriasis|Immunomodulation |
NCT01736696 |
A 6-Month Study Of CP-690,550 Versus Tacrolimus In Kidney Transplant Patients |
Completed |
Kidney Transplantation |
NCT00106639 |
Long-Term, Open-Label Study Of CP-690,550 For Treatment Of Rheumatoid Arthritis In Japan |
Completed |
Rheumatoid Arthritis |
NCT00661661 |
A Long Term Study To Evaluate The Safety And Tolerability Of CP-690,550 For Patients With Moderate To Severe Chronic Plaque Psoriasis |
Terminated |
Psoriasis |
NCT01163253 |
Extension Study Of Stage 1 Subjects Of Study A3921009 For The Prevention Of Acute Rejection In Kidney Transplant Patient |
Completed |
Kidney Transplantation |
NCT00263328 |
A Study To Investigate Safety And Efficacy Of CP-690,550 For Induction Therapy In Subjects With Moderate To Severe Crohn's Disease |
Completed |
Crohn's Disease |
NCT01393626 |
A Study Evaluating The Efficacy And Safety Of CP-690,550 In Asian Subjects With Moderate To Severe Plaque Psoriasis |
Completed |
Psoriasis |
NCT01815424 |
A One-Year Study To Evaluate The Efficacy And Safety Of CP-690,550 For Patients With Moderate To Severe Chronic Plaque Psoriasis |
Completed |
Psoriasis |
NCT01309737 |
A One-Year Study To Evaluate The Effects And Safety Of CP-690,550 In Patients With Moderate To Severe Chronic Plaque Psoriasis |
Completed |
Psoriasis |
NCT01276639 |
A Long Term Study To Evaluate The Safety, Tolerability And Efficacy Of CP-690,550 In Patients With Moderate To Severe Plaque Psoriasis And/Or Psoriatic Arthritis |
Completed |
Psoriasis |
NCT01519089 |
A Study Of Oral CP-690,550 As A Maintenance Therapy For Ulcerative Colitis |
Completed |
Ulcerative Colitis |
NCT01458574 |
A Study To Evaluate The Effects And Safety Of Treatment, Treatment Withdrawal, Followed By Re-Treatment With CP-690,550 In Subjects With Moderate To Severe Chronic Plaque Psoriasis |
Completed |
Psoriasis |
NCT01186744 |
Extension Study Of Subjects From Study A3921030 For The Prevention Of Acute Rejection In Kidney Transplant Patients |
Completed |
Kidney Transplantation |
NCT00658359 |
The Impact of Targeted Therapy on Microorganism in Patients With Psoriasis |
Unknown status |
Psoriasis |
NCT01504113 |
A Phase 3, Multi Site, Randomized, Double Blind, Placebo Controlled Study Of The Efficacy And Safety Comparing CP- 690,550 And Etanercept In Subjects With Moderate To Severe Chronic Plaque Psoriasis |
Completed |
Psoriasis |
NCT01241591 |
JAKPOT (JAK Inhibitors and Predictors of Outcome in rheumaToid Arthritis) |
Recruiting |
Rheumatoid Arthritis |
NCT04084223 |
Pharmacokinetics Of CP-690,550 In Patients With Impaired Renal Function |
Completed |
Renal Impairment |
NCT01740362 |
A Study Of CP-690,550 In Stable Kidney Transplant Patients |
Completed |
Kidney Transplant |
NCT01710033 |
Pharmacokinetics And Dialysability Of CP-690,550 In Subjects With End-Stage Renal Disease |
Completed |
End-Stage Renal Disease|Hemodialysis |
NCT01710020 |
Long-Term Study Of CP-690,550 In Subjects With Ulcerative Colitis |
Active, not recruiting |
Ulcerative Colitis |
NCT01470612 |
A Open-Label Study Of CP-690,550 As Long-Term Therapy (48 Weeks) In Subjects With Crohn's Disease |
Completed |
Crohn's Disease |
NCT01470599 |
A Study To Compare The Amount Of CP-690,550 That Is Absorbed Into The Blood Of Healthy Subjects Following Oral Administration Of Two Different Strength Tablets Of CP-690,550 |
Completed |
Arthritis, Rheumatoid |
NCT01277991 |
CP-690-550 Ointment For Chronic Plaque Psoriasis |
Completed |
Psoriasis |
NCT01246583 |
Pharmacokinetics And Safety Study Of Two CP-690,550 Controlled Release Formulation Following Single Dose In Healthy Volunteers |
Completed |
Healthy |
NCT01185184 |
CP-690,550 Pharmacokinetics In Healthy Chinese Subjects |
Completed |
Healthy |
NCT01101919 |
A Study Of The Taste Of Different Oral Liquid Preparations Of CP-690,550 In Trained Adult Product Testers |
Completed |
Arthritis, Rheumatoid |
NCT01023100 |
A Safety and Tolerability Study of CP-690,550 in Subjects With Hepatic Impairment and Normal Hepatic Function |
Completed |
Hepatic Insufficiency |
NCT00969813 |
A Study Comparing 2 Doses Of CP-690,550 Vs. Placebo For The Treatment Of Rheumatoid Arthritis In Patients On Other Background Arthritis Medications |
Completed |
Arthritis, Rheumatoid |
NCT00856544 |
A Phase 3 Study Comparing 2 Doses of CP-690,550 vs. Placebo for Treatment of Rheumatoid Arthritis |
Completed |
Arthritis, Rheumatoid |
NCT00814307 |
Comparison Of 5 CP-690,550 Doses Vs. Placebo, For The Treatment Of Rheumatoid Arthritis In Japan |
Completed |
Arthritis, Rheumatoid |
NCT00687193 |
Topical CP-690,550 For Chronic Plaque Psoriasis |
Completed |
Psoriasis |
NCT00678561 |
Effectiveness and Safety of 3 Dosing Regimens of CP-690,550 to Placebo in Subjects With Moderate to Severe Chronic Plaque Psoriasis |
Completed |
Psoriasis |
NCT00678210 |
A Study to Investigate the Safety and Efficacy of CP-690,550 in Patients With Moderate to Severe Crohn's Disease |
Completed |
Crohn's Disease |
NCT00615199 |
Clinical Study to Evaluate the Pharmacokinetic Profiles and Safety of CKD-374 5 mg in Healthy Volunteers |
Completed |
Rheumatoid Arthritis |
NCT03858725 |
Long-Term Safety Follow-Up Of Subjects Previously Enrolled In Rheumatoid Arthritis Studies Of CP-690,550 |
Completed |
Arthritis, Rheumatoid |
NCT00414661 |
Three Dose Levels of CP-690,550 Monotherapy Versus Placebo, Administered Orally Twice Daily (BID) for 6 Weeks |
Completed |
Rheumatoid Arthritis |
NCT00147498 |
In Vitro Evaluation of a Novel Drug on Airway Epithelial Cells Obtained From Participants With Severe Asthma |
Completed |
Asthma |
NCT02740049 |
Effect Of CP-690,550 On The Pharmacokinetics Of Metformin In Healthy Volunteers |
Completed |
Rheumatoid Arthritis |
NCT01405118 |
Study Of The Effects Of Atorvastatin On Cholesterol Levels In Rheumatoid Arthritis Patients Taking CP-690,550 |
Completed |
Rheumatoid Arthritis |
NCT01059864 |
A Study To Evaluate The Mechanism Of Action Of CP-690,550 In Patients With Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT00976599 |
Study of CP-690,550 Versus Placebo In Rheumatoid Arthritis Patients On Background Methotrexate With Inadequate Response To Tumor Necrosis Factor (TNF) Inhibitors |
Completed |
Arthritis, Rheumatoid |
NCT00960440 |
CP-690,550 and Midazolam Drug-Drug Interaction Study |
Completed |
Healthy Volunteer |
NCT00902460 |
A Phase 3 Study Comparing 2 Doses Of CP-690,550 And The Active Comparator, Humira (Adalimumab) Vs. Placebo For Treatment Of Rheumatoid Arthritis |
Completed |
Rheumatoid Arthritis |
NCT00853385 |
A 2-Year Phase 3 Study Of CP-690,550 In Patients With Active Rheumatoid Arthritis On Background Methotrexate |
Completed |
Arthritis, Rheumatoid |
NCT00847613 |
Comparison Of 4 CP-690,550 Doses Vs. Placebo, Each Combined With Methotrexate, For The Treatment Of Rheumatoid Arthritis in Japan |
Completed |
Arthritis, Rheumatoid |
NCT00603512 |
A Phase 2 Study For Patients With A Physician's Diagnosis Of Rheumatoid Arthritis |
Completed |
Arthritis, Rheumatoid |
NCT00550446 |
Comparison Of 6 CP-690,550 Doses Vs.Placebo, Each Combined With Methotrexate, For The Treatment Of Rheumatoid Arthritis |
Completed |
Arthritis, Rheumatoid |
NCT00413660 |
A Time to Cardiovascular Event Analysis Comparing Tocilizumab to Other Biologics in Patients With Rheumatoid Arthritis (RA) |
Unknown status |
Rheumatoid Arthritis |
NCT02797769 |
Determination of the Optimal Treatment Target in Ulcerative Colitis |
Recruiting |
Colitis, Ulcerative |
NCT04259138 |
A Phase II, Dose Ranging Study Of CP-690,550 Eye Drops In Patients With Dry Eye Disease |
Completed |
Dry Eye Syndromes |
NCT01135511 |
Comparing The Effectiveness And Safety Of 2 Doses Of An Experimental Drug, CP-690,550, To Methotrexate (MTX) In Patients With Rheumatoid Arthritis Who Have Not Previously Received MTX |
Completed |
Arthritis, Rheumatoid |
NCT01039688 |
CP-690,550 Thorough QTc Study |
Completed |
Healthy |
NCT01743677 |
A Prospective, Randomized, Placebo and Active Comparator Controlled Study of CP-690,550 in Subjects With Dry Eye. |
Completed |
Dry Eye Syndromes |
NCT00784719 |
Study of a JAK3 Inhibitor for the Prevention of Acute Rejection in Kidney Transplant Patients |
Completed |
Kidney Transplantation |
NCT00483756 |
CP-690,550 And Oral Contraception Drug-Drug Interaction Study |
Completed |
Healthy |
NCT01137708 |
A Study To Assess the Immune Response Following Administration Of Influenza and Pneumococcal Vaccines To Subjects With Rheumatoid Arthritis Receiving CP-690,550 Or Placebo |
Completed |
Rheumatoid Arthritis |
NCT01359150 |
A Phase I Open-Label Study of the Effects of Tacrolimus and Cyclosporine on CP-690,555 in Healthy Volunteers |
Completed |
Healthy Volunteers |
NCT00860496 |
A Study to Observe Vedolizumab and Anti-tumour Necrosis Factors (Anti-TNFs) Outcomes in Real-world Biologic Ulcerative Colitis (UC) and Crohn's Disease (CD) Participants |
Recruiting |
Colitis, Ulcerative|Crohn Disease |
NCT03710486 |
Enhancing Patient Ability to Understand and Utilize Complex Information Concerning Medication Self-management |
Completed |
Rheumatoid Arthritis |
NCT02820038 |