Tofacitinib History and Updates

243 events · 2004 – present

Synced daily from openFDA and ClinicalTrials.gov. Last sync: .

51
FDA Approvals
8
Label Revisions
636
Trial Milestones
7
Pivotal Publications
Tofacitinib — history and updatesFDA approvals, label revisions, recalls, trials, and pivotal publicationsFDA approvalsLabel revisionsRecalls + safetyTrialsPublications2004200520062007200820092010201120122013201420152016201720182019202020212022202320242025202620272028202920302031Trial: NCT07522801 2026-09-01 → 2029-12-01 (primary completion)Trial: NCT07352566 2026-08-01 → 2030-06-01 (primary completion)Trial: NCT07055529 2026-06-01 → 2026-12-31 (primary completion)Trial: NCT07581418 2026-06-01 → 2026-12-01 (primary completion)Trial: NCT07598643 2026-05-31 → 2030-08-31 (primary completion)Trial: NCT07406035 2026-04-30 → 2027-08-31 (primary completion)Trial: NCT07547930 2026-04-24 → 2027-12-30 (primary completion)Trial: NCT07530367 2026-04-01 → 2028-04-01 (primary completion)Trial: NCT07313072 2026-03-31 → 2027-01-31 (primary completion)Trial: NCT07406204 2026-02-15 → 2026-08-15 (primary completion)Trial: NCT07343635 2026-02-01 → 2027-07-01 (primary completion)Trial: NCT06654882 2026-01-09 → 2026-12-31 (primary completion)Trial: NCT07487311 2026-01-07 → 2027-12-31 (primary completion)Trial: NCT07297069 2026-01-01 → 2027-05-31 (primary completion)Trial: NCT07211932 2025-12-31 → 2026-12-31 (primary completion)Trial: NCT07281456 2025-12-18 → 2030-12-15 (primary completion)Trial: NCT07554820 2025-12-06 → 2026-08-31 (primary completion)Trial: NCT07131813 2025-10-10 → 2027-01-01 (primary completion)Trial: NCT07138898 2025-09-30 → 2027-09-30 (primary completion)Trial: NCT07261306 2025-08-29 → 2025-12-10 (primary completion)Trial: NCT06945666 2025-08-01 → 2027-01-31 (primary completion)Trial: NCT04871191 2025-06-06 → 2028-10-31 (primary completion)Trial: NCT06979271 2025-06-01 → 2026-04-30 (primary completion)Trial: NCT07008846 2025-05-10 → 2026-09-30 (primary completion)Trial: NCT06923228 2025-04-21 → 2025-07-30 (primary completion)Trial: NCT06698822 2025-03-10 → 2026-10-19 (primary completion)Trial: NCT06998875 2025-03-01 → 2025-10-31 (primary completion)Trial: NCT07044141 2025-03-01 → 2025-09-30 (primary completion)Trial: NCT06465732 2025-01-31 → 2025-11-30 (primary completion)Trial: NCT06687551 2025-01-01 → 2029-04-01 (primary completion)Trial: NCT07472166 2024-12-21 → 2025-08-30 (primary completion)Trial: NCT06810050 2024-12-18 → 2025-08-30 (primary completion)Trial: NCT06707246 2024-12-15 → 2026-10-31 (primary completion)Trial: NCT06689982 2024-12-01 → 2025-12-01 (primary completion)Trial: NCT06625450 2024-10-31 → 2025-12-31 (primary completion)Trial: NCT06301373 2024-09-01 → 2030-04-01 (primary completion)Trial: NCT06573593 2024-07-29 → 2026-12-31 (primary completion)Trial: NCT06393972 2024-07-01 → 2025-11-30 (primary completion)Trial: NCT06498089 2024-06-28 → 2026-06-30 (primary completion)Trial: NCT06095128 2024-06-12 → 2027-07-09 (primary completion)Trial: NCT06418529 2024-05-15 → 2024-07-19 (primary completion)Trial: NCT06201715 2024-05-01 → 2025-06-30 (primary completion)Trial: NCT05754710 2024-04-12 → 2026-09-30 (primary completion)Trial: NCT06438679 2024-03-19 → 2024-09-30 (primary completion)Trial: NCT06176508 2024-02-26 → 2026-04-28 (primary completion)Trial: NCT06172361 2024-01-20 → 2025-09-30 (primary completion)Trial: NCT06044844 2023-11-30 → 2024-05-31 (primary completion)Trial: NCT06202560 2023-11-29 → 2024-07-10 (primary completion)Trial: NCT06020144 2023-11-15 → 2026-07-31 (primary completion)Trial: NCT06112665 2023-11-10 → 2025-03-31 (primary completion)Trial: NCT06114407 2023-10-30 → 2024-06-30 (primary completion)Trial: NCT06011343 2023-10-01 → 2024-10-01 (primary completion)Trial: NCT06119490 2023-07-05 → 2026-07-31 (primary completion)Trial: NCT06278402 2023-07-01 → 2024-01-06 (primary completion)Trial: NCT05112263 2023-07-01 → 2025-12-01 (primary completion)Trial: NCT05662228 2023-06-29 → 2026-12-31 (primary completion)Trial: NCT05845723 2023-06-01 → 2026-06-01 (primary completion)Trial: NCT05814939 2023-04-26 → 2024-05-11 (primary completion)Trial: NCT05803135 2023-03-31 → 2025-01-30 (primary completion)Trial: NCT05749666 2023-01-20 → 2025-07-20 (primary completion)Trial: NCT05625581 2022-11-10 → 2024-12-31 (primary completion)Trial: NCT05487963 2022-11-09 → 2023-06-30 (primary completion)Trial: NCT05326464 2022-10-07 → 2025-06-16 (primary completion)Trial: NCT05048238 2022-09-30 → 2024-02-15 (primary completion)Trial: NCT05104723 2022-08-12 → 2026-05-04 (primary completion)Trial: NCT05246293 2022-08-08 → 2024-03-02 (primary completion)Trial: NCT06157905 2022-08-06 → 2023-02-05 (primary completion)Trial: NCT06474078 2022-08-01 → 2025-06-20 (primary completion)Trial: NCT05165771 2022-07-31 → 2023-02-28 (primary completion)Trial: NCT05400889 2022-06-10 → 2023-03-01 (primary completion)Trial: NCT05606107 2022-05-20 → 2024-06-30 (primary completion)Trial: NCT05348213 2022-05-16 → 2025-06-01 (primary completion)Trial: NCT05431283 2022-04-25 → 2022-12-31 (primary completion)Trial: NCT05728008 2022-04-05 → 2022-06-05 (primary completion)Trial: NCT05313620 2022-04-01 → 2025-12-31 (primary completion)Trial: NCT04768504 2022-03-22 → 2024-01-17 (primary completion)Trial: NCT05133297 2022-02-16 → 2022-12-19 (primary completion)Trial: NCT05186623 2022-02-05 → 2026-12-31 (primary completion)Trial: NCT04876781 2022-01-12 → 2026-06-30 (primary completion)Trial: NCT05151848 2022-01-05 → 2026-01-15 (primary completion)Trial: NCT06310057 2022-01-01 → 2024-03-01 (primary completion)Trial: NCT05087589 2021-11-20 → 2023-01-01 (primary completion)Trial: NCT05080218 2021-11-15 → 2024-04-04 (primary completion)Trial: NCT05102448 2021-11-01 → 2025-12-31 (primary completion)Trial: NCT04624230 2021-08-12 → 2027-04-28 (primary completion)Trial: NCT04985955 2021-07-30 → 2021-09-21 (primary completion)Trial: NCT04944524 2021-07-01 → 2024-07-01 (primary completion)Trial: NCT04925973 2021-06-01 → 2023-12-31 (primary completion)Trial: NCT04927000 2021-05-31 → 2022-08-30 (primary completion)Trial: NCT04496960 2021-05-18 → 2025-01-14 (primary completion)Trial: NCT04798287 2021-03-10 → 2021-12-31 (primary completion)Trial: NCT04772248 2021-02-22 → 2021-12-30 (primary completion)Trial: NCT04580277 2021-01-25 → 2022-12-01 (primary completion)Trial: NCT04721821 2021-01-22 → 2021-11-29 (primary completion)Trial: NCT04799262 2021-01-01 → 2022-03-16 (primary completion)Trial: NCT04424303 2020-12-04 → 2025-12-08 (primary completion)Trial: NCT04311567 2020-11-07 → 2023-11-30 (primary completion)Trial: NCT04246372 2020-10-21 → 2024-10-30 (primary completion)Trial: NCT04610476 2020-10-19 → 2024-10-19 (primary completion)Trial: NCT04468425 2020-10-14 → 2020-12-21 (primary completion)Trial: NCT04415151 2020-10-14 → 2021-02-28 (primary completion)Trial: NCT04613219 2020-10-01 → 2023-04-30 (primary completion)Trial: NCT04469114 2020-09-16 → 2021-01-09 (primary completion)Trial: NCT04338204 2020-09-14 → 2026-03-30 (primary completion)Trial: NCT04552197 2020-09-02 → 2020-12-29 (primary completion)Trial: NCT04529876 2020-08-17 → 2021-08-31 (primary completion)Trial: NCT07101471 2020-08-04 → 2025-06-11 (primary completion)Trial: NCT04062695 2020-08-04 → 2023-12-31 (primary completion)Trial: NCT04413617 2020-07-29 → 2022-02-07 (primary completion)Trial: NCT04412252 2020-07-06 → 2020-09-16 (primary completion)Trial: NCT04390061 2020-06-30 → 2020-09-30 (primary completion)Trial: NCT04338711 2020-06-17 → 2020-09-15 (primary completion)Trial: NCT05638932 2020-06-16 → 2023-09-25 (primary completion)Trial: NCT04431895 2020-06-11 → 2024-03-21 (primary completion)Trial: NCT04750317 2020-05-11 → 2020-08-01 (primary completion)Trial: NCT04449224 2020-04-27 → 2023-08-19 (primary completion)Trial: NCT04332042 2020-04-10 → 2020-06-20 (primary completion)Trial: NCT04299971 2020-03-01 → 2022-12-31 (primary completion)Trial: NCT04928066 2020-03-01 → 2023-06-30 (primary completion)Trial: NCT03976245 2020-03-01 → 2025-03-31 (primary completion)Trial: NCT04175886 2020-02-25 → 2023-05-08 (primary completion)Trial: NCT04141904 2020-02-10 → 2022-05-23 (primary completion)Trial: NCT04973033 2019-12-01 → 2021-01-31 (primary completion)Trial: NCT04114461 2019-11-06 → 2019-12-04 (primary completion)Trial: NCT04485325 2019-11-04 → 2024-03-31 (primary completion)Trial: NCT04111614 2019-10-11 → 2019-12-12 (primary completion)Trial: NCT03885713 2019-09-10 → 2024-12-31 (primary completion)Trial: NCT03681275 2019-09-03 → 2025-11-30 (primary completion)Trial: NCT04034238 2019-08-29 → 2020-12-01 (primary completion)Trial: NCT04464642 2019-07-10 → 2020-08-31 (primary completion)Trial: NCT03970837 2019-06-05 → 2021-10-29 (primary completion)Trial: NCT03980483 2019-05-16 → 2021-09-15 (primary completion)Trial: NCT03793439 2019-05-15 → 2020-06-24 (primary completion)Trial: NCT03910543 2019-04-11 → 2021-06-01 (primary completion)Trial: NCT03580343 2019-04-04 → 2019-12-01 (primary completion)Trial: NCT03868072 2019-02-22 → 2019-03-29 (primary completion)Trial: NCT03800979 2019-01-12 → 2021-01-30 (primary completion)Trial: NCT03981900 2019-01-04 → 2023-02-06 (primary completion)Trial: NCT03598959 2019-01-01 → 2019-12-31 (primary completion)Trial: NCT04403776 2018-12-03 → 2019-02-12 (primary completion)Trial: NCT03755466 2018-11-21 → 2023-11-20 (primary completion)Trial: NCT03486457 2018-08-10 → 2021-04-28 (primary completion)Trial: NCT03502616 2018-06-07 → 2019-12-19 (primary completion)Trial: NCT03000439 2018-05-10 → 2024-03-27 (primary completion)Trial: NCT03504072 2018-01-16 → 2019-06-30 (primary completion)Trial: NCT03387423 2017-11-02 → 2023-07-17 (primary completion)Trial: NCT03440892 2017-11-01 → 2025-01-31 (primary completion)Trial: NCT03274076 2017-09-25 → 2019-04-08 (primary completion)Trial: NCT03736161 2017-09-15 → 2019-09-28 (primary completion)Trial: NCT03112148 2017-09-11 → 2017-11-15 (primary completion)Trial: NCT03738956 2017-09-01 → 2018-12-30 (primary completion)Trial: NCT03288324 2017-08-23 → 2022-11-01 (primary completion)Trial: NCT03103412 2017-05-04 → 2017-11-08 (primary completion)Trial: NCT03159936 2017-04-03 → 2020-05-13 (primary completion)Trial: NCT03002649 2017-01-31 → 2020-09-30 (primary completion)Trial: NCT06688838 2017-01-01 → 2026-12-31 (primary completion)Trial: NCT02996500 2016-11-10 → 2018-08-15 (primary completion)Trial: NCT03011281 2016-09-30 → 2020-12-31 (primary completion)Trial: NCT02812342 2016-09-30 → 2018-07-31 (primary completion)Trial: NCT02592434 2016-06-10 → 2019-05-16 (primary completion)Trial: NCT02321930 2016-02-16 → 2017-09-29 (primary completion)Trial: NCT02535689 2015-08-28 → 2018-04-26 (primary completion)Trial: NCT02487433 2015-06-30 → 2015-07-31 (primary completion)Trial: NCT02566967 2015-05-31 → 2017-12-31 (primary completion)Trial: NCT02299297 2015-01-31 → 2017-12-31 (primary completion)Trial: NCT02312882 2014-12-31 → 2015-08-31 (primary completion)Trial: NCT02281552 2014-11-18 → 2017-03-15 (primary completion)Trial: NCT02193815 2014-09-30 → 2015-02-28 (primary completion)Trial: NCT02187055 2014-08-31 → 2016-12-31 (primary completion)Trial: NCT02197455 2014-07-31 → 2015-07-31 (primary completion)Trial: NCT02147587 2014-06-30 → 2015-06-30 (primary completion)Trial: NCT02157012 2014-05-31 → 2022-04-30 (primary completion)Trial: NCT02084875 2014-04-11 → 2014-05-25 (primary completion)Trial: NCT02092467 2014-03-14 → 2020-07-22 (primary completion)Trial: NCT01976364 2014-02-17 → 2019-05-20 (primary completion)Trial: NCT01877668 2014-01-20 → 2015-12-18 (primary completion)Trial: NCT02001181 2013-12-31 → 2014-09-30 (primary completion)Trial: NCT01882439 2013-08-31 → 2016-04-30 (primary completion)Trial: NCT01932372 2013-07-26 → 2021-08-24 (primary completion)Trial: NCT01831466 2013-05-31 → 2014-09-30 (primary completion)Trial: NCT01786668 2013-04-30 → 2015-03-31 (primary completion)Trial: NCT01710046 2013-03-31 → 2013-11-30 (primary completion)Trial: NCT01500551 2013-03-18 → 2025-02-12 (primary completion)Trial: NCT01731327 2012-11-30 → 2012-12-31 (primary completion)Trial: NCT01741493 2012-11-30 → 2013-12-31 (primary completion)Trial: NCT01458951 2012-06-30 → 2015-05-31 (primary completion)Trial: NCT01599377 2012-05-31 → 2012-07-31 (primary completion)Trial: NCT01465763 2012-04-30 → 2015-05-31 (primary completion)Trial: NCT01499004 2011-11-30 → 2011-12-31 (primary completion)Trial: NCT01375127 2011-08-31 → 2012-07-31 (primary completion)Trial: NCT01164579 2010-10-31 → 2013-11-30 (primary completion)FDA approval — 2012-11-06 FDA approved Xeljanz (tofacitinib) (NDA 203214) Sponsor: PF PRISM CV. Class: Type 1 - New Molecular Entity.FDA approval (supplemental) — 2013-05-03 FDA approved supplemental application for Xeljanz (tofacitinib) — Manufacturing (CMC) (NDA 203214 S-1) Sponsor: PF PRISM CV. Class: Manufacturing (CMC).FDA approval (supplemental) — 2013-11-08 FDA approved supplemental application for Xeljanz (tofacitinib) — REMS (NDA 203214 S-6) Sponsor: PF PRISM CV. Class: REMS.FDA approval (supplemental) — 2013-11-18 FDA approved supplemental application for Xeljanz (tofacitinib) — Efficacy (NDA 203214 S-2) Sponsor: PF PRISM CV. Class: Efficacy.FDA approval (supplemental) — 2014-02-21 FDA approved supplemental application for Xeljanz (tofacitinib) — Efficacy (NDA 203214 S-4) Sponsor: PF PRISM CV. Class: Efficacy.FDA approval (supplemental) — 2014-03-26 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 203214 S-5) Sponsor: PF PRISM CV. Class: Labeling.FDA approval (supplemental) — 2014-05-07 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 203214 S-7) Sponsor: PF PRISM CV. Class: Labeling.FDA approval (supplemental) — 2015-02-11 FDA approved supplemental application for Xeljanz (tofacitinib) — REMS (NDA 203214 S-8) Sponsor: PF PRISM CV. Class: REMS.FDA approval (supplemental) — 2015-06-19 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 203214 S-10) Sponsor: PF PRISM CV. Class: Labeling.FDA approval (supplemental) — 2015-12-22 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 203214 S-11) Sponsor: PF PRISM CV. Class: Labeling.FDA approval (supplemental) — 2016-02-08 FDA approved supplemental application for Xeljanz (tofacitinib) — REMS (NDA 203214 S-13) Sponsor: PF PRISM CV. Class: REMS.FDA approval — 2016-02-23 FDA approved Xeljanz Xr (tofacitinib) (NDA 208246) Sponsor: PFIZER. Class: Type 3 - New Dosage Form.FDA approval (supplemental) — 2017-08-22 FDA approved supplemental application for Xeljanz Xr (tofacitinib) — Efficacy (NDA 208246 S-1) Sponsor: PFIZER. Class: Efficacy.FDA approval (supplemental) — 2017-08-22 FDA approved supplemental application for Xeljanz (tofacitinib) — Efficacy (NDA 203214 S-14) Sponsor: PF PRISM CV. Class: Efficacy.FDA approval (supplemental) — 2017-08-22 FDA approved supplemental application for Xeljanz Xr (tofacitinib) — Labeling (NDA 208246 S-2) Sponsor: PFIZER. Class: Labeling.FDA approval (supplemental) — 2017-08-22 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 203214 S-16) Sponsor: PF PRISM CV. Class: Labeling.FDA approval (supplemental) — 2017-12-14 FDA approved supplemental application for Xeljanz Xr (tofacitinib) — Efficacy (NDA 208246 S-3) Sponsor: PFIZER. Class: Efficacy.FDA approval (supplemental) — 2017-12-14 FDA approved supplemental application for Xeljanz (tofacitinib) — Efficacy (NDA 203214 S-17) Sponsor: PF PRISM CV. Class: Efficacy.FDA approval (supplemental) — 2018-05-30 FDA approved supplemental application for Xeljanz (tofacitinib) — Efficacy (NDA 203214 S-18) Sponsor: PF PRISM CV. Class: Efficacy.FDA approval (supplemental) — 2018-08-17 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 203214 S-21) Sponsor: PF PRISM CV. Class: Labeling.FDA approval (supplemental) — 2018-08-17 FDA approved supplemental application for Xeljanz Xr (tofacitinib) — Labeling (NDA 208246 S-7) Sponsor: PFIZER. Class: Labeling.FDA approval (supplemental) — 2018-10-18 FDA approved supplemental application for Xeljanz Xr (tofacitinib) — Labeling (NDA 208246 S-6) Sponsor: PFIZER. Class: Labeling.FDA approval (supplemental) — 2018-10-18 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 203214 S-20) Sponsor: PF PRISM CV. Class: Labeling.FDA approval (supplemental) — 2019-07-25 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 203214 S-24) Sponsor: PF PRISM CV. Class: Labeling.FDA approval (supplemental) — 2019-07-25 FDA approved supplemental application for Xeljanz Xr (tofacitinib) — Labeling (NDA 208246 S-10) Sponsor: PFIZER. Class: Labeling.FDA approval (supplemental) — 2019-08-30 FDA approved supplemental application for Xeljanz Xr (tofacitinib) — Labeling (NDA 208246 S-11) Sponsor: PFIZER. Class: Labeling.FDA approval (supplemental) — 2019-08-30 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 203214 S-23) Sponsor: PF PRISM CV. Class: Labeling.FDA approval (supplemental) — 2019-12-12 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 203214 S-25) Sponsor: PF PRISM CV. Class: Labeling.FDA approval (supplemental) — 2019-12-12 FDA approved supplemental application for Xeljanz Xr (tofacitinib) — Efficacy (NDA 208246 S-9) Sponsor: PFIZER. Class: Efficacy.FDA approval (supplemental) — 2020-09-25 FDA approved supplemental application for Xeljanz (tofacitinib) — Efficacy (NDA 203214 S-26) Sponsor: PF PRISM CV. Class: Efficacy.FDA approval — 2020-09-25 FDA approved Xeljanz (tofacitinib) (NDA 213082) Sponsor: PFIZER. Class: Type 3 - New Dosage Form.FDA approval (supplemental) — 2021-12-02 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 213082 S-4) Sponsor: PFIZER. Class: Labeling.FDA approval (supplemental) — 2021-12-02 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 203214 S-31) Sponsor: PF PRISM CV. Class: Labeling.FDA approval (supplemental) — 2021-12-02 FDA approved supplemental application for Xeljanz Xr (tofacitinib) — Labeling (NDA 208246 S-17) Sponsor: PFIZER. Class: Labeling.FDA approval (supplemental) — 2021-12-14 FDA approved supplemental application for Xeljanz Xr (tofacitinib) — Efficacy (NDA 208246 S-13) Sponsor: PFIZER. Class: Efficacy.FDA approval (supplemental) — 2021-12-14 FDA approved supplemental application for Xeljanz (tofacitinib) — Efficacy (NDA 203214 S-28) Sponsor: PF PRISM CV. Class: Efficacy.FDA approval (supplemental) — 2021-12-14 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 213082 S-3) Sponsor: PFIZER. Class: Labeling.FDA approval (supplemental) — 2024-05-14 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 203214 S-34) Sponsor: PF PRISM CV. Class: Labeling.FDA approval (supplemental) — 2024-05-14 FDA approved supplemental application for Xeljanz Xr (tofacitinib) — Labeling (NDA 208246 S-21) Sponsor: PFIZER. Class: Labeling.FDA approval (supplemental) — 2024-05-14 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 213082 S-6) Sponsor: PFIZER. Class: Labeling.FDA approval (supplemental) — 2024-09-27 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 203214 S-36) Sponsor: PF PRISM CV. Class: Labeling.FDA approval (supplemental) — 2024-09-27 FDA approved supplemental application for Xeljanz Xr (tofacitinib) — Labeling (NDA 208246 S-23) Sponsor: PFIZER. Class: Labeling.FDA approval (supplemental) — 2024-09-27 FDA approved supplemental application for Xeljanz (tofacitinib) — Labeling (NDA 213082 S-8) Sponsor: PFIZER. Class: Labeling.FDA approval (supplemental) — 2025-02-21 FDA approved supplemental application for Xeljanz (tofacitinib) — Efficacy (NDA 203214 S-38) Sponsor: PF PRISM CV. Class: Efficacy.FDA approval (supplemental) — 2025-02-21 FDA approved supplemental application for Xeljanz Xr (tofacitinib) — Efficacy (NDA 208246 S-25) Sponsor: PFIZER. Class: Efficacy.FDA approval (supplemental) — 2025-02-21 FDA approved supplemental application for Xeljanz (tofacitinib) — Efficacy (NDA 213082 S-10) Sponsor: PFIZER. Class: Efficacy.FDA approval (supplemental) — 2025-10-16 FDA approved supplemental application for Xeljanz (tofacitinib) — Efficacy (NDA 213082 S-11) Sponsor: PFIZER. Class: Efficacy.FDA approval (supplemental) — 2025-10-16 FDA approved supplemental application for Xeljanz (tofacitinib) — Efficacy (NDA 203214 S-39) Sponsor: PF PRISM CV. Class: Efficacy.FDA approval (supplemental) — 2026-03-06 FDA approved supplemental application for Xeljanz Xr (tofacitinib) — Efficacy (NDA 208246 S-27) Sponsor: PFIZER. Class: Efficacy.FDA approval (supplemental) — 2026-03-06 FDA approved supplemental application for Xeljanz (tofacitinib) — Efficacy (NDA 203214 S-41) Sponsor: PF PRISM CV. Class: Efficacy.FDA approval (supplemental) — 2026-03-06 FDA approved supplemental application for Xeljanz (tofacitinib) — Efficacy (NDA 213082 S-13) Sponsor: PFIZER. Class: Efficacy.Label revision — 2026-05-31 Boxed warning present on label on TOFACITINIB label (effective 2026-05-31) WARNING: SERIOUS INFECTIONS, MORTALITY, MALIGNANCY, MAJOR ADVERSE CARDIOVASCULAR EVENTS, and THROMBOSIS SERIOUS INFECTIONS Patients treated with tofacitinib oral solution is at increased risk for developing serious bacterial, fungal, viral,Label revision — 2026-06-02 Boxed warning present on label on TOFACITINIB label (effective 2026-06-02) WARNING: SERIOUS INFECTIONS, MORTALITY, MALIGNANCY, MAJOR ADVERSE CARDIOVASCULAR EVENTS, and THROMBOSIS SERIOUS INFECTIONS Patients treated with tofacitinib tablets are at increased risk for developing serious bacterial, fungal, viral, and Label revision — 2026-06-04 Boxed warning present on label on TOFACITINIB label (effective 2026-06-04) WARNING: SERIOUS INFECTIONS, MORTALITY, MALIGNANCY, MAJOR ADVERSE CARDIOVASCULAR EVENTS, and THROMBOSIS SERIOUS INFECTIONS Patients treated with tofacitinib tablets are at increased risk for developing serious bacterial, fungal, viral, and Label revision — 2026-06-04 Boxed warning present on label on TOFACITINIB label (effective 2026-06-04) WARNING: SERIOUS INFECTIONS, MORTALITY, MALIGNANCY, MAJOR ADVERSE CARDIOVASCULAR EVENTS, and THROMBOSIS SERIOUS INFECTIONS Patients treated with tofacitinib tablets are at increased risk for developing serious bacterial, fungal, viral, and Label revision — 2026-06-05 Boxed warning present on label on tofacitinib label (effective 2026-06-05) WARNING: SERIOUS INFECTIONS, MORTALITY, MALIGNANCY, MAJOR ADVERSE CARDIOVASCULAR EVENTS, and THROMBOSIS SERIOUS INFECTIONS Patients treated with tofacitinib tablets are at increased risk for developing serious bacterial, fungal, viral, and Label revision — 2026-06-05 Boxed warning present on label on TOFACITINIB label (effective 2026-06-05) WARNING: SERIOUS INFECTIONS, MORTALITY, MALIGNANCY, MAJOR ADVERSE CARDIOVASCULAR EVENTS, and THROMBOSIS SERIOUS INFECTIONS Patients treated with tofacitinib extended-release tablets are at increased risk for developing serious bacterial, fuLabel revision — 2026-06-08 Boxed warning present on label on Tofacitinib label (effective 2026-06-08) WARNING: SERIOUS INFECTIONS, MORTALITY, MALIGNANCY, MAJOR ADVERSE CARDIOVASCULAR EVENTS, and THROMBOSIS SERIOUS INFECTIONS Patients treated with tofacitinib extended-release tablets are at increased risk for developing serious bacterial, fuLabel revision — 2026-06-09 Boxed warning present on label on Tofacitinib label (effective 2026-06-09) WARNING: SERIOUS INFECTIONS, MORTALITY, MALIGNANCY, MAJOR ADVERSE CARDIOVASCULAR EVENTS, and THROMBOSIS SERIOUS INFECTIONS Patients treated with tofacitinib extended-release tablets are at increased risk for developing serious bacterial, fuResults posted — 2012-12-07 Trial results posted: NCT01745055 Co-Administration Of Methotrexate And CP-690,550Results posted — 2013-02-20 Trial results posted: NCT01736696 Multiple Dose Escalation Study In Medically Stable Subjects With PsoriasisResults posted — 2013-08-14 Trial results posted: NCT01375127 Collection of Follow-up Data From CP-690,550-treated Kidney Transplant RecipientsResults posted — 2015-04-13 Trial results posted: NCT01710046 Study Of The Mechanism Of Action Of CP-690,550 In The Skin Of Subjects With Moderate To Severe Chronic Plaque PsoriasisResults posted — 2015-04-22 Trial results posted: NCT01164579 Effects of Tofacitinib (CP-690,550) on Magnetic Resonance Imaging (MRI)- Assessed Joint Structure In Early Rheumatoid Arthritis (RA)Results posted — 2015-10-15 Trial results posted: NCT02001181 Tofacitinib Ointment For Atopic Dermatitis (Atopic Eczema)Results posted — 2015-11-25 Trial results posted: NCT01831466 Tofacitinib Ointment For Chronic Plaque PsoriasisResults posted — 2016-06-01 Trial results posted: NCT01458951 A Study To Evaluate Both The Efficacy and Safety Profile of CP-690,550 In Patients With Moderately to Severely Active Ulcerative ColitisResults posted — 2016-06-07 Trial results posted: NCT01465763 A Study Evaluating The Efficacy And Safety Of CP-690,550 In Patients With Moderate To Severe Ulcerative ColitisResults posted — 2016-06-09 Trial results posted: NCT02193815 A 12 Day Study To Evaluate A Topical Drug To Treat Plaque PsoriasisResults posted — 2016-06-10 Trial results posted: NCT01786668 Dose-Ranging Study Of Tofacitinib In Adults With Active Ankylosing SpondylitisResults posted — 2017-04-04 Trial results posted: NCT02197455 Tofacitnib for the Treatment of Alopecia Areata and VariantsResults posted — 2017-07-06 Trial results posted: NCT01877668 Efficacy And Safety Of Tofacitinib In Psoriatic Arthritis: Comparator StudyResults posted — 2017-09-15 Trial results posted: NCT01882439 Tofacitinib In Psoriatic Arthritis Subjects With Inadequate Response to TNF InhibitorsResults posted — 2017-11-06 Trial results posted: NCT02312882 Tofacitinib for the Treatment of Alopecia Areata and Its VariantsResults posted — 2018-04-11 Trial results posted: NCT02147587 A Study to Assess Immune Response Following Zoster Vaccination to Subjects With Rheumatoid Arthritis Receiving Tofacitinib or Placebo With BResults posted — 2018-06-27 Trial results posted: NCT02187055 An Efficacy And Safety Study Evaluating Tofacitinib With And Without Methotrexate Compared To Adalimumab With MethotrexateResults posted — 2018-10-10 Trial results posted: NCT02812342 Topical Tofacitinib for the Treatment of Alopecia Areata and Its VariantsResults posted — 2018-10-12 Trial results posted: NCT02281552 A Study To Evaluate The Safety And Efficacy Of Tofacitinib Modified Release Tablets Compared To Tofacitinib Immediate Release Tablets In AduResults posted — 2019-03-19 Trial results posted: NCT02321930 Musculoskeletal Ultrasound Assessment of Therapeutic Response of Tofacitinib in Rheumatoid Arthritis PatientsResults posted — 2019-05-07 Trial results posted: NCT02299297 Study To Evaluate The Efficacy Of Tofacitinib In Moderate To Severe Alopecia Areata, Totalis And UniversalisResults posted — 2020-02-21 Trial results posted: NCT02592434 Efficacy Study Of Tofacitinib In Pediatric JIA PopulationResults posted — 2020-02-27 Trial results posted: NCT02996500 Safety and Efficacy of Pf-06650833 In Subjects With Rheumatoid Arthritis, With An Inadequate Response To MethotrexateResults posted — 2020-05-08 Trial results posted: NCT03274076 Evaluation of Tofacitinib in Early Diffuse Cutaneous Systemic Sclerosis (dcSSc)Results posted — 2020-05-21 Trial results posted: NCT01976364 Open-Label Extension Study Of Tofacitinib In Psoriatic ArthritisResults posted — 2021-01-11 Trial results posted: NCT03502616 Efficacy and Safety of Tofacitinib in Subjects With Active Ankylosing Spondylitis (AS)Results posted — 2021-02-01 Trial results posted: NCT03580343 Tofacitinib for Inflammatory Eye DiseaseResults posted — 2021-08-17 Trial results posted: NCT02092467 Safety Study Of Tofacitinib Versus Tumor Necrosis Factor (TNF) Inhibitor In Subjects With Rheumatoid ArthritisResults posted — 2022-02-08 Trial results posted: NCT04034238 Mesothelin-Targeted Immunotoxin LMB-100 in Combination With Tofacitinib in Persons With Previously Treated Pancreatic Adenocarcinoma, CholanResults posted — 2022-02-18 Trial results posted: NCT03793439 Tofacitinib Hypothesis-generating, Pilot Study for Corticosteroid-Dependent SarcoidosisResults posted — 2022-03-10 Trial results posted: NCT03800979 Effectiveness and Safety of Tofacitinib in Patients With Extensive and Recalcitrant Alopecia AreataResults posted — 2023-04-07 Trial results posted: NCT04413617 TO ASSESS THE EFFICACY AND SAFETY OF PF-06650833, PF-06651600, AND TOFACITINIB ALONE AND IN COMBINATION IN PARTICIPANTS WITH ACTIVE RHEUMATOResults posted — 2023-10-25 Trial results posted: NCT03980483 Efficacy and Safety of GSK3196165 Versus Placebo and Tofacitinib in Participants With Moderately to Severely Active Rheumatoid Arthritis WhoResults posted — 2023-11-30 Trial results posted: NCT03970837 Efficacy and Safety of GSK3196165 Versus Placebo and Tofacitinib in Participants With Moderately to Severely Active Rheumatoid Arthritis WhoResults posted — 2024-02-08 Trial results posted: NCT03486457 Efficacy And Safety Of Tofacitinib In Chinese Subjects With Active Psoriatic ArthritisResults posted — 2024-04-04 Trial results posted: NCT04580277 Tofacitinib For Treatment Of Chronic PouchitisResults posted — 2024-04-12 Trial results posted: NCT04721821 Comparative Effectiveness Of Tumor Necrosis Factor Inhibitors And Tofacitinib Use In Earlier Lines Of Therapy And Use As Monotherapy.Results posted — 2024-07-30 Trial results posted: NCT03288324 Open-label Study of Tofacitinib for Moderate to Severe Skin Involvement in Young Adults With LupusResults posted — 2024-10-01 Trial results posted: NCT03981900 IDentification of Factors Predictive of Tofacitinib's Survival in Patient With Rheumatoid ArthritisResults posted — 2024-10-21 Trial results posted: NCT03387423 Observational Study to Determine How Physicians Make Treatment Decisions in Patients Treated With Tofacitinib for Moderate to Severe Active Results posted — 2024-10-26 Trial results posted: NCT01932372 Tofacitinib (Xeljanz) Special Investigation for Rheumatoid ArthritisResults posted — 2025-03-21 Trial results posted: NCT05048238 Evaluation of Tofacitinib in Prevention of Photosensitivity in LupusResults posted — 2025-03-28 Trial results posted: NCT04415151 Tofacitinib for Treatment of Moderate COVID-19Results posted — 2025-05-30 Trial results posted: NCT06202560 Effectiveness and Safety of Tofacitinib in Patients With Recalcitrant Frontal Fibrosing Alopecia : A Pilot StudyResults posted — 2025-06-03 Trial results posted: NCT03000439 A Safety, Efficacy And Pharmacokinetics Study Of Tofacitinib In Pediatric Patients With sJIAResults posted — 2025-07-31 Trial results posted: NCT06418529 A Study to Understand How Effective is Tofacitinib When Compared to Other Advanced Treatments in Patients With Rheumatoid ArthritisResults posted — 2025-09-16 Trial results posted: NCT06474078 Study To Evaluate The Efficacy Of Tofacitinib In Patients With SJS/TENResults posted — 2025-12-11 Trial results posted: NCT04246372 Tofacitinib for Immune Skin Conditions in Down SyndromeResults posted — 2025-12-18 Trial results posted: NCT04496960 Safety of Tofacitinib, an Oral Janus Kinase Inhibitor, in Primary Sjogren's SyndromeResults posted — 2026-03-23 Trial results posted: NCT01500551 Long-Term Safety Study Of Tofacitinib In Patients With Juvenile Idiopathic ArthritisPivotal publication — 2010-01-01 Rituximab versus cyclophosphamide for ANCA-associated vasculitis. (N Engl J Med) SATELITE — Study of Salvage Therapy to Treat Patients With Granulomatosis With PolyangiitisPivotal publication — 2017-01-01 Tofacitinib as Induction and Maintenance Therapy for Ulcerative Colitis. (N Engl J Med) OCTAVE — A Study To Evaluate Both The Efficacy and Safety Profile of CP-690,550 In Patients With Moderately to Severely Active Ulcerative ColitisPivotal publication — 2017-01-01 Tofacitinib or Adalimumab versus Placebo for Psoriatic Arthritis. (N Engl J Med) PsOLSET-BD — Safety and Efficacy of Tofacitinib vs Methotrexate in the Treatment of Psoriatic ArthritisPivotal publication — 2017-01-01 Tofacitinib for Psoriatic Arthritis in Patients with an Inadequate Response to TNF Inhibitors. (N Engl J Med) PsOLSET-BD — Safety and Efficacy of Tofacitinib vs Methotrexate in the Treatment of Psoriatic ArthritisPivotal publication — 2021-01-01 Tofacitinib in Patients Hospitalized with Covid-19 Pneumonia. (N Engl J Med) Tofacitinib in Hospitalized Patients With COVID-19 PneumoniaPivotal publication — 2022-01-01 Tofacitinib in juvenile idiopathic arthritis: a double-blind, placebo-controlled, withdrawal phase 3 randomised trial. (Lancet) Efficacy Study Of Tofacitinib In Pediatric JIA PopulationPivotal publication — 2022-01-01 Effect of Tocilizumab on Disease Activity in Patients With Active Polymyalgia Rheumatica Receiving Glucocorticoid Therapy: A Randomized Clinical Trial. (JAMA) ITTGPMR — Induction and Tapering Therapy With Tofacitinib and Glucocorticoid in Patients With Polymyalgia Rheumaticatoday (2026-06-12)FDA approvalLabel revisionRecall or safetyTrial activityPivotal publication

Source: openFDA, ClinicalTrials.gov via AACT, PubMed · Hipa.ai, 2026-06-12Download chart as PNG

This page tracks every FDA action, clinical trial milestone, and major publication for Tofacitinib since 2004, drawn from openFDA, ClinicalTrials.gov, and PubMed.

All published updates (34)

2025

Upcoming & expected milestones

Primary completion· ClinicalTrials.gov
A Randomized, Controlled, Open-label, Multicenter Clinical Trial Comparing the Efficacy and Safety of a Precision Treatment Regimen Based on
Primary completion· ClinicalTrials.gov
A Phase 3 Study Comparing TLL-018 to Tofacitinib in RA Subjects With Inadequate Response or Intolerance to bDMARDs
Primary completion· ClinicalTrials.gov
Evaluation of the Efficacy and Safety of Methylprednisolone Combined With the JAK Inhibitors in the Treatment of Toxic Epidermal Necrolysis
Primary completion· ClinicalTrials.gov
Major Adverse Cardiovascular Events (MACE) in Rheumatoid Arthritis Patient With Moderate to Severe Disease Activity Treated With Tofacitinib
Primary completion· ClinicalTrials.gov
Efficacy of Tofacitinib, Methotrexate Combination Therapy Versus Upadacitinib, Methotrexate Combination Therapy in Moderate to Severe Rheuma
Primary completion· ClinicalTrials.gov
Korea Xeljanz Post-marketing Surveillance for Juvenile Idiopathic Arthritis
Primary completion· ClinicalTrials.gov
A Phase 2 Trial to Assess Safety and Efficacy of Tofacitinib 2% Cream in the Treatment of Cutaneous T-cell Lymphoma (CTCL), Stages IA, IB, a
Primary completion· ClinicalTrials.gov
A Randomized Trial Comparing the Efficacy and Safety of Secukinumab with Tofacitinib in the Treatment of Moderate to Severe Hidradenitis Sup
Primary completion· ClinicalTrials.gov
Comparison of Efficacy and Safety Psoralen Combined With Ultraviolet A (PUVA) Vs Tofacitinib in the Treatment of Generalized Vitiligo.
Primary completion· ClinicalTrials.gov
Prediction Model for Response to Biologics and Small Molecular Agent for UC
Primary completion· ClinicalTrials.gov
Evaluation of Oral Tofacitinib in Children Aged 2 to 17 Years Old Suffering From Moderate to Severe Ulcerative Colitis
Primary completion· ClinicalTrials.gov
Evaluation of Oral Tofacitinib in Children Aged 2 to 17 Years Old Suffering From Moderate to Severe Ulcerative Colitis
Primary completion· ClinicalTrials.gov
The Efficacy and Safety of Anti-inflammation Treatment (Hirudoid Introduction Followed by Yellow Light Therapy) Combined With Tofacitinib an
Primary completion· ClinicalTrials.gov
A Phase II Clinical Trial to Evaluate the Efficacy and Safety of TQH3906 Capsules in the Treatment of Active Psoriatic Arthritis
Primary completion· ClinicalTrials.gov
A Prospective Cohort Study Evaluating the Efficacy and Safety of Guselkumab (GUS) With JAK Inhibitors in Patients With Difficult-To-Treat In
Primary completion· ClinicalTrials.gov
A Phase III Randomized Controlled Trial Evaluating the Efficacy and Safety of Tofacitinib Combined With Imatinib in Patients With Moderate-t

Past events

2026
Trial started· ClinicalTrials.gov
Comparison of Efficacy and Safety Psoralen Combined With Ultraviolet A (PUVA) Vs Tofacitinib in the Treatment of Generalized Vitiligo.
Trial started· ClinicalTrials.gov
Modulation of the Immune System in Down Syndrome for Improved Outcomes and Neurodevelopment - 1
Primary completion· ClinicalTrials.gov
Efficacy and Safety of Telitacicept Combined With Tofacitinib for Refractory Rheumatoid Arthritis
Trial started· ClinicalTrials.gov
A Phase II Clinical Trial to Evaluate the Efficacy and Safety of TQH3906 Capsules in the Treatment of Active Psoriatic Arthritis
Trial started· ClinicalTrials.gov
A Phase III Randomized Controlled Trial Evaluating the Efficacy and Safety of Tofacitinib Combined With Imatinib in Patients With Moderate-t
Primary completion· ClinicalTrials.gov
Observational Study To Assess The Effectiveness and Treatment Adherence Of Tofacitinib of Ulcerative Colitis In Clinical Practice In Sweden
Trial started· ClinicalTrials.gov
The Efficacy and Safety of Anti-inflammation Treatment (Hirudoid Introduction Followed by Yellow Light Therapy) Combined With Tofacitinib an
Primary completion· ClinicalTrials.gov
A Phase 3 Study Comparing TLL-018 to Tofacitinib in RA Subjects With Inadequate Response or Intolerance to bDMARDs
Trial started· ClinicalTrials.gov
A Prospective Cohort Study Evaluating the Efficacy and Safety of Guselkumab (GUS) With JAK Inhibitors in Patients With Difficult-To-Treat In
Trial started· ClinicalTrials.gov
Combination Therapy With Infliximab and Tofacitinib for Acute Severe Ulcerative Colitis - CINTO Trial
2025
Trial started· ClinicalTrials.gov
Major Adverse Cardiovascular Events (MACE) in Rheumatoid Arthritis Patient With Moderate to Severe Disease Activity Treated With Tofacitinib
Primary completion· ClinicalTrials.gov
Tofacitinib Versus Cyclosporine for Steroid Refractory Acute Severe Ulcerative Colitis
Primary completion· ClinicalTrials.gov
The Efficacy and Safety of Tofacitinib in Patients With Glucocorticoid Resistant ICIs-related Myocarditis
Trial started· ClinicalTrials.gov
Evaluation of Efficacy and Safety of add-on Tofacitinib in Patients With Oral Lichen Planus
Primary completion· ClinicalTrials.gov
Induction and Tapering Therapy With Tofacitinib and Glucocorticoid in Patients With Polymyalgia Rheumatica
Primary completion· ClinicalTrials.gov
Observational Study To Assess The Effectiveness and Treatment Adherence Of Tofacitinib of Ulcerative Colitis In Clinical Practice In Sweden
Trial started· ClinicalTrials.gov
Immunosuppressant Management in Rheumatology Patients Undergoing Elective Total Shoulder Arthroplasty
Primary completion· ClinicalTrials.gov
Phase 2b Safety and Efficacy Study of CGB-500 Topical Ointment With 0.5% and 1% Tofacitnib for Treatment of Atopic Dermatitis
Primary completion· ClinicalTrials.gov
Efficacy of Tofacitinib on Skin Thickening in Diffuse Cutaneous Systemic Sclerosis: A Comparative Study With Methotrexate
Results posted· ClinicalTrials.gov
A Study to Understand How Effective is Tofacitinib When Compared to Other Advanced Treatments in Patients With Rheumatoid Arthritis
Primary completion· ClinicalTrials.gov
A Study to Assess Efficacy and Safety of CGB-500, 1% Tofacitinib Versus an Active Comparator for Atopic Dermatitis
Results posted· ClinicalTrials.gov
A Safety, Efficacy And Pharmacokinetics Study Of Tofacitinib In Pediatric Patients With sJIA
Trial started· ClinicalTrials.gov
Efficacy and Safety of Telitacicept Combined With Tofacitinib for Refractory Rheumatoid Arthritis
Results posted· ClinicalTrials.gov
Effectiveness and Safety of Tofacitinib in Patients With Recalcitrant Frontal Fibrosing Alopecia : A Pilot Study
Trial started· ClinicalTrials.gov
Efficacy of Tofacitinib, Methotrexate Combination Therapy Versus Upadacitinib, Methotrexate Combination Therapy in Moderate to Severe Rheuma
Trial started· ClinicalTrials.gov
A Study to Assess Efficacy and Safety of CGB-500, 1% Tofacitinib Versus an Active Comparator for Atopic Dermatitis
Trial started· ClinicalTrials.gov
A Phase 2 Trial to Assess Safety and Efficacy of Tofacitinib 2% Cream in the Treatment of Cutaneous T-cell Lymphoma (CTCL), Stages IA, IB, a
Primary completion· ClinicalTrials.gov
A Phase 3 Study Comparing TLL-018 to Tofacitinib in RA Subjects With Inadequate Response or Intolerance to bDMARDs
Trial started· ClinicalTrials.gov
Efficacy and Safety of Dupilumab in Combination With Tofacitinib in Moderate to Severe Adult AD Patients
Primary completion· ClinicalTrials.gov
Effects of Antirheumatic Treatment on Levels of Survivin in Rheumatoid Arthritis Patients
2024
Primary completion· ClinicalTrials.gov
Identification of Predictive Biomarkers for Response to Biologic Therapies and Tofacitinib in Inflammatory Bowel Disease
Trial started· ClinicalTrials.gov
Efficacy of Tofacitinib on Skin Thickening in Diffuse Cutaneous Systemic Sclerosis: A Comparative Study With Methotrexate
Trial started· ClinicalTrials.gov
Phase 2b Safety and Efficacy Study of CGB-500 Topical Ointment With 0.5% and 1% Tofacitnib for Treatment of Atopic Dermatitis
Trial started· ClinicalTrials.gov
A Randomized Trial Comparing the Efficacy and Safety of Secukinumab with Tofacitinib in the Treatment of Moderate to Severe Hidradenitis Sup
Results posted· ClinicalTrials.gov
Observational Study to Determine How Physicians Make Treatment Decisions in Patients Treated With Tofacitinib for Moderate to Severe Active
Primary completion· ClinicalTrials.gov
Impact of Tapering Immunosuppressants on Maintaining Minimal Disease Activity in Adult Subjects With Psoriatic Arthritis
Results posted· ClinicalTrials.gov
IDentification of Factors Predictive of Tofacitinib's Survival in Patient With Rheumatoid Arthritis
Results posted· ClinicalTrials.gov
Open-label Study of Tofacitinib for Moderate to Severe Skin Involvement in Young Adults With Lupus
Trial started· ClinicalTrials.gov
Efficacy and Safety of JAK Inhibitors in Patients With AA: RWE Study
Primary completion· ClinicalTrials.gov
A Study to Understand How Effective is Tofacitinib When Compared to Other Advanced Treatments in Patients With Rheumatoid Arthritis
Primary completion· ClinicalTrials.gov
Effectiveness and Safety of Tofacitinib in Patients With Recalcitrant Frontal Fibrosing Alopecia : A Pilot Study
Trial started· ClinicalTrials.gov
The Efficacy and Safety of Tofacitinib in Patients With Glucocorticoid Resistant ICIs-related Myocarditis
Primary completion· ClinicalTrials.gov
To Compare the Efficacy and Safety of Low-dose Glucocorticoids and Tofacitinib in Alleviating Moderate to High Disease Activity Rheumatoid A
Primary completion· ClinicalTrials.gov
Baricitinib in the Treatment of Refractory Axial Spondyloarthritis Patients: A Comparison With Tofacitinib
Trial started· ClinicalTrials.gov
A Randomized, Controlled, Open-label, Multicenter Clinical Trial Comparing the Efficacy and Safety of a Precision Treatment Regimen Based on
Trial started· ClinicalTrials.gov
A Study to Understand How Effective is Tofacitinib When Compared to Other Advanced Treatments in Patients With Rheumatoid Arthritis
Trial started· ClinicalTrials.gov
Korea Xeljanz Post-marketing Surveillance for Juvenile Idiopathic Arthritis
Results posted· ClinicalTrials.gov
Comparative Effectiveness Of Tumor Necrosis Factor Inhibitors And Tofacitinib Use In Earlier Lines Of Therapy And Use As Monotherapy.
Primary completion· ClinicalTrials.gov
Capability of Tofacitinib or Etanercept to Accelerate Tapering of NSAID and Treat-to-target Guided De-escalation of Corticosteroids in RA Pa
Trial started· ClinicalTrials.gov
Efficacy and Safety of HS-10374 Compared to Placebo in Adults With Active Psoriatic Arthritis
Results posted· ClinicalTrials.gov
Efficacy And Safety Of Tofacitinib In Chinese Subjects With Active Psoriatic Arthritis
Trial started· ClinicalTrials.gov
Induction and Tapering Therapy With Tofacitinib and Glucocorticoid in Patients With Polymyalgia Rheumatica
Primary completion· ClinicalTrials.gov
Tofacitinib for the Treatment of Refractory Immune-related Colitis from Checkpoint Inhibitor Therapy- TRICK Study
Primary completion· ClinicalTrials.gov
Efficacy of Oral Tofacitinib in Moderate to Severe Alopecia Areata, Totalis and Universalis at Tertiary Care Hospital, Karachi.
2023
Primary completion· ClinicalTrials.gov
Tofacitinib for Reduction of Spinal Inflammation in Patients With Psoriatic ArthritiS PresenTing With Axial InvOlvement
Results posted· ClinicalTrials.gov
Efficacy and Safety of GSK3196165 Versus Placebo and Tofacitinib in Participants With Moderately to Severely Active Rheumatoid Arthritis Who
Trial started· ClinicalTrials.gov
Effectiveness and Safety of Tofacitinib in Patients With Recalcitrant Frontal Fibrosing Alopecia : A Pilot Study
Trial started· ClinicalTrials.gov
A Phase 3 Study Comparing TLL-018 to Tofacitinib in RA Subjects With Inadequate Response or Intolerance to bDMARDs

Sources

FDA approvals, label revisions, and recalls come from the public openFDA APIs (Drugs@FDA, Drug Label, Drug Enforcement). Drug-safety communications come from the FDA RSS feed. Trial milestones come from ClinicalTrials.gov via the AACT pg dump. Pivotal-publication events come from PubMed, filtered to high-impact journals linked to a Phase 3 trial in our inventory.