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T

T. Ishii

Researcher at Eli Lilly and Company

Publications -  10
Citations -  920

T. Ishii is an academic researcher from Eli Lilly and Company. The author has contributed to research in topics: Rheumatoid arthritis & Context (language use). The author has an hindex of 7, co-authored 10 publications receiving 674 citations.

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Baricitinib versus Placebo or Adalimumab in Rheumatoid Arthritis

TL;DR: In patients with rheumatoid arthritis who had had an inadequate response to methotrexate, baricitinib was associated with significant clinical improvements as compared with placebo and adalimumab.
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Safety Profile of Baricitinib in Patients with Active Rheumatoid Arthritis with over 2 Years Median Time in Treatment

TL;DR: In this integrated analysis of patients with moderate to severe active RA with exposure up to 5.5 years, baricitinib has an acceptable safety profile in the context of demonstrated efficacy.
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Safety profile of baricitinib in Japanese patients with active rheumatoid arthritis with over 1.6 years median time in treatment: An integrated analysis of Phases 2 and 3 trials

TL;DR: In Japanese patients, herpes zoster was more frequent than that of patients overall in the integrated database, but the events were considered manageable, and baricitinib had acceptable safety profile in Japanese RA patients in the context of demonstrated efficacy.
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Efficacy and safety of baricitinib in Japanese patients with active rheumatoid arthritis: A 52-week, randomized, single-blind, extension study.

TL;DR: The efficacy and safety profile of baricitinib was maintained during long-term treatment of Japanese patients with RA and background methotrexate therapy and increases in the American College of Rheumatology response rates observed during the first 12 weeks were maintained during the extension period.
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Efficacy and safety of baricitinib in Japanese patients with rheumatoid arthritis: Subgroup analyses of four multinational phase 3 randomized trials.

TL;DR: Data for baricitinib, with/without methotrexate, in Japanese subpopulations across all stages of the RA treatment continuum accord with the efficacy/safety profile in overall study populations.