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临床试验/CTRI/2022/05/042887
CTRI/2022/05/042887尚未招募4 期

Efficacy and safety of Tofacitinib in Ankylosing Spondylitis and its correlation with Serum Cytokines- A randomized, double- blind, placebo controlled trial.

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试验速览

阶段
4 期
状态
尚未招募
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1.Age >= 18 years and < 60 years satisfying presence of Ankylosing Spondylitis based on the Modified New York Criteria for Ankylosing Spondylitis (1984).
  • 2.Has active disease on screening at baseline defined by BASDAI >= 4 and Back pain score (BASDAI Question 2) of ï?³4.
  • 3.Inadequate response to NSAID- Has received at least two NSAIDs for a total duration of at least 4 weeks and lack of sufficient clinical response based on clinical judgement.
  • 4.Patients having intolerance to atleast two different oral NSAIDs.
  • 5.Patient not affording for biologicals like TNF inhibitors or IL-17 inhibitors recommended for treatment of ankylosing spondylitis.

排除标准

  • 1.Subjects that have been exposed to or are currently receiving JAK inhibitors or biological DMARDS
  • 2.Blood dyscrasias at screening
  • 2.1Hemoglobin <10 g/dL
  • 2.2Absolute white blood cell count (WBC) <3.0 x 109/L ( <3000 mm3)
  • 2.3Absolute neutrophil count (ANC) <1.5 x 109/L ( <1500 mm3)
  • 2.4Absolute lymphocyte count <1.0 x 109/L ( <1000/mm3)
  • 2.5Platelet count <100 x 109/L ( <100,000/mm3)
  • 3.Estimated Creatinine Clearance <40 mL/min based on Cockcroft Gault equation at Screening
  • 4.Total bilirubin, AST or ALT more than 1.5 times the upper limit of normal (ULN) at screening
  • 5.History of any other autoimmune rheumatic disease.
  • 6.History of known or suspected complete ankylosis of the spine.
  • 7.Patients having active tuberculosis or positive for latent tuberculosis as tested by QuantiFERON-TB Gold In Tube (QFT Gold test) or Montoux skin Test
  • 8.History of recurrent herpes zoster or herpes simplex.
  • 9.History of severe infection requiring hospitalization or parenteral antimicrobial therapy
  • 10.History of lymphoproliferative disorder, such as Epstein Barr Virus related lymphoproliferative disease (EBV-LPD), history of lymphoma, leukemia
  • 11.Patient with increased risk for GI perforation
  • 12.Present malignancy or with a history of malignancy, with the exception of adequately treated or excised non metastatic basal cell or squamous cell cancer of the skin or cervical carcinoma in situ.
  • 13.Pregnant female or breast feeding mothers.

研究者

发起方
none

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