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Xpanding The Possibilities1

An Oral Therapy With The Efficacy of A Biologic2

   

   

Xeljanz® demonstrated similar treatment effectiveness to biological DMARDS2

   

*P values are for one-sided noninferiority comparisons (98.34% confidence interval) and must be <0.025 to declare significance.2,3

   

  

ACR, American College of Rheumatology; BID, twice daily; IR, inadequate responders; LOCF, last observation carried forward; MTX, methotrexate; NRI, nonresponder imputation; NS, nonsignificant; q 2 wk, every 2 weeks; Sc, subcutaneous.

  

References:

Dhillon S. Tofacitinib: A Review in Rheumatoid Arthritis. Drugs. 2017;77(18):1987-2001.Fleischmann R, Mysler E, Hall S, et al; on behalf of the ORAL Strategy Investigators. Efficacy and safety of tofacitinib monotherapy, tofacitinib with methotrexate, and adalimumab with methotrexate in patients with rheumatoid arthritis (ORAL Strategy): a phase 3b/4, double-blind, head-to-head, randomised controlled trial. Lancet. 2017;390(10093):457-468.Data on file. Pfizer Inc, New York, NY.

  

Please click the Prescribing Information link to view the safety and adverse events information of Xeljanz®.
For the use only of Registered Medical Practitioners or a Hospital or a Laboratory.

PP-XEL-IND-0843 22/07/22
Clinical Efficacy RA

About

XELJANZ® (tofacitinib citrate) is a small molecule that selectively targets the JAK pathway

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Dosing & Administration

   

Helps protect against RA, PsA and UC

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For more details on, Who is a Registered Medical Practitioner*, please visit https://cdsco.gov.in/opencms/export/sites/CDSCO_WEB/Pdf-documents/acts_rules/2016DrugsandCosmeticsAct1940Rules1945.pdf , Page No. 39, Rule 2 part (ee), last accessed on 13th September 2019.
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