46. Malignant rheumatoid arthritis Clinical trials / Disease details
Clinical trials : 4,356 / Drugs : 2,567 - (DrugBank : 415) / Drug target genes : 192 - Drug target pathways : 228
Showing 1 to 10 of 140 diseases
No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
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1 | NCT05165771 (ClinicalTrials.gov) | July 2022 | 8/12/2021 | 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 Study to Evaluate Safety, Tolerability, and Efficacy of GS-5718 in Participants With Active Rheumato ... | A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Phase 2 Proof-of-Concept Study to Evaluate Safety, Tolerability, and Efficacy of GS-5718 on Background Therapy With Conventional Synthetic Disease-modifying Antirheumatic Drug(s) (csDMARDs) in Participants With Active Rheumatoid Arthritis Who Have an Inadequate Response to Biologic DMARD(s) Treatment A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Phase 2 Proof-of-Concept Study to Evalu ... | Rheumatoid Arthritis | Drug: GS-5718;Drug: Placebo to match GS-5718;Drug: Tofacitinib 5 mg;Drug: Placebo to match Tofacitinib Drug: GS-5718;Drug: Placebo to match GS-5718;Drug: Tofacitinib5 mg;Drug: Placebo to match Tofacitini ... | Gilead Sciences | NULL | Withdrawn | 18 Years | 75 Years | All | 0 | Phase 2 | NULL |
2 | NCT05606107 (ClinicalTrials.gov) | May 20, 2022 | 1/11/2022 | To Compare the Efficacy and Safety of Low-dose Glucocorticoids and Tofacitinib in Alleviating Moderate to High Disease Activity Rheumatoid Arthritis for 24 Weeks To Compare the Efficacy and Safety of Low-dose Glucocorticoids and Tofacitinibin Alleviating Moderat ... | To Compare the Efficacy and Safety of Low-dose Glucocorticoids and Tofacitinib in Alleviating Moderate to High Disease Activity Rheumatoid Arthritis for 24 Weeks To Compare the Efficacy and Safety of Low-dose Glucocorticoids and Tofacitinibin Alleviating Moderat ... | Rheumatoid Arthritis | Drug: Tofacitinib;Drug: Glucocorticoid | Second Affiliated Hospital, School of Medicine, Zhejiang University | Jiaxing Hospital of T.C.M;Jinhua Municipal Central Hospital;SAHZU.CHANGXING CAMPUS;Zhuji People's hospital;Shaoxing People's Hospital Jiaxing Hospital of T.C.M;Jinhua Municipal Central Hospital;SAHZU.CHANGXING CAMPUS;Zhuji People's ho ... | Recruiting | 18 Years | 70 Years | All | 230 | Phase 4 | China |
3 | NCT05246293 (ClinicalTrials.gov) | April 1, 2022 | 17/1/2022 | Tofacitinib in the Treatment of Rheumatoid Arthritis-related Interstitial Lung Disease. | Safety and Tolerability of Tofacitinib in the Treatment of Rheumatoid Arthritis-related Interstitial Lung Disease (RAILDTo Trial). Safety and Tolerability of Tofacitinibin the Treatment of Rheumatoid Arthritis-related Interstitial ... | Rheumatoid Arthritis;Interstitial Lung Disease | Drug: Tofacitinib | National Institute of Respiratory Diseases, Mexico | NULL | Recruiting | 18 Years | N/A | All | 60 | Phase 2 | Mexico |
4 | NCT05133297 (ClinicalTrials.gov) | February 16, 2022 | 15/11/2021 | The Safety and Efficacy of TLL-018 in Active Rheumatoid Arthritis | A Phase 2A, Randomized, Double-blind, Double-dummy, Tofacitinib-parallel-group Study to Evaluate the Safety and Efficacy of TLL-018 in Active Rheumatoid Arthritis Who Had an Inadequate Response or Intolerance to Methotrexate. A Phase 2A, Randomized, Double-blind, Double-dummy, Tofacitinib-parallel-group Study to Evaluate the ... | Rheumatoid Arthritis | Drug: TLL-018;Drug: Tofacitinib | Hangzhou Highlightll Pharmaceutical Co., Ltd | NULL | Recruiting | 18 Years | 75 Years | All | 100 | Phase 2 | China |
5 | EUCTR2021-004131-84-NL (EUCTR) | 14/02/2022 | 08/09/2021 | Comparing the effectiveness of tofacitinib extended release (XR) chronotherapy, morning versus evening dosing, in rheumatoid arthritis (RA) and psoriatic arthritis (PsA) patients from a patient’s, clinical as well as a translational point of view. Comparing the effectiveness of tofacitinibextended release (XR) chronotherapy, morning versus evenin ... | Chronotherapy in Inflammatory Arthritis (ChronIA trial): a crossover randomized controlled trial comparing the effectiveness of morning and evening dosing of tofacitinib extended-release - ChronIA trial Chronotherapy in Inflammatory Arthritis (ChronIA trial): a crossover randomized controlled trial com ... | Rheumatoid arthritis or psoriatic arthritis according to respectively 2010 criteria or CASPAR criteria MedDRA version: 23.1;Level: PT;Classification code 10039073;Term: Rheumatoid arthritis;System Organ Class: 10028395 - Musculoskeletal and connective tissue disorders MedDRA version: 21.0;Level: LLT;Classification code 10037160;Term: Psoriatic arthritis;System Organ Class: 10028395 - Musculoskeletal and connective tissue disorders;Therapeutic area: Diseases [C] - Immune System Diseases [C20] Rheumatoid arthritis or psoriatic arthritis according to respectively 2010 criteria or CASPAR criter ... | Trade Name: Xeljanz XR Product Name: Tofacitinib XR Product Code: EMEA/H/C/004214 | Erasmus Medical Center | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 84 | Phase 4 | Netherlands | ||
6 | NCT04876781 (ClinicalTrials.gov) | January 12, 2022 | 20/4/2021 | Korean Post-marketing Surveillance for Xeljanz XR | Korean Post-marketing Surveillance for Xeljanz XR (Registered) | Active Moderate to Severe Rheumatoid Arthritis;Active Ankylosing Spondylitis | Drug: Tofacitinib XR | Pfizer | NULL | Recruiting | 18 Years | N/A | All | 200 | Korea, Republic of | |
7 | ChiCTR2100054220 | 2021-12-04 | 2021-12-11 | Efficacy and safety of tofacitinib in the treatment of rheumatoid arthritis related interstitial lung disease Efficacy and safety of tofacitinibin the treatment of rheumatoid arthritis related interstitial lung ... | Efficacy and safety of tofacitinib in the treatment of rheumatoid arthritis related interstitial lung disease Efficacy and safety of tofacitinibin the treatment of rheumatoid arthritis related interstitial lung ... | Rheumatoid arthritis related interstitial lung disease | Tofacitinib group:No;Traditional immunosuppressive therapy group:No; | Yantai Yuhuangding Hospital | NULL | Recruiting | 18 | 90 | Both | Tofacitinib group:30;Traditional immunosuppressive therapy group:30; | Phase 4 | Chian |
8 | NCT05080218 (ClinicalTrials.gov) | November 15, 2021 | 6/10/2021 | COVID-19 VaccinE Response in Rheumatology Patients | The SARS-CoV-2 Vaccine Response and Safety in Rheumatology Patients and the Influence of Temporary Interruptions in Immunomodulatory Therapy The SARS-CoV-2 Vaccine Response and Safety in Rheumatology Patients and the Influence of Temporary I ... | Rheumatoid Arthritis;Psoriatic Arthritis;Spondylarthritis | Drug: Upadacitinib;Drug: Abatacept;Drug: Secukinumab;Drug: Tofacitinib;Drug: TNF Inhibitor;Drug: Canakinumab Injection;Drug: Baricitinib;Drug: Ixekizumab Drug: Upadacitinib;Drug: Abatacept;Drug: Secukinumab;Drug: Tofacitinib;Drug: TNF Inhibitor;Drug: Can ... | Jeffrey Curtis | University of Alabama at Birmingham;University of Nebraska;University of Pennsylvania;AbbVie;Bristol-Myers Squibb;Novartis;Eli Lilly and Company;Pfizer University of Alabama at Birmingham;University of Nebraska;University of Pennsylvania;AbbVie;Bristol ... | Recruiting | 18 Years | 85 Years | All | 1000 | Phase 4 | United States |
9 | EUCTR2021-001560-14-ES (EUCTR) | 13/08/2021 | 11/06/2021 | Use of tofacitinib in patients with treatment-refractory rheumatoid arthritis. | Single-center, open-label, uncontrolled clinical trial to evaluate the association between the expression of the JAK / STAT pathway and the response to tofacitinib in patients with refractory rheumatoid arthritis. Single-center, open-label, uncontrolled clinical trial to evaluate the association between the expre ... | Refractory rheumatoid arthritis;Therapeutic area: Diseases [C] - Immune System Diseases [C20] | Trade Name: XELJANZ INN or Proposed INN: TOFACITINIB | FUNDACION JIMENEZ DIAZ HEALTH RESEARCH INSTITUTE | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 42 | Phase 4 | Spain | ||
10 | ChiCTR2100048185 | 2021-07-01 | 2021-07-04 | The efficacy and safety of Tofacitinib in the treatment of DMARDS naive rheumatoid arthtits patients | The efficacy and safety of Tofacitinib virus MTX in the treatment of DMARDS naive rheumatoid arthtits patients--a randomized controlled trial The efficacy and safety of Tofacitinibvirus MTX in the treatment of DMARDS naive rheumatoid arthtits ... | Rheumatoid Arthritis | Experimental group:Tofacitinib 5mg twice per day;Control group:Methotrexate; | Peking University First Hospital | NULL | Pending | 18 | Both | Experimental group:112;Control group:112; | Phase 4 | China |