Ireland
--:--IST
Latest
Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: 2025 Eurostat Trade Data and Economic Impact Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: 2025 Eurostat Trade Data and Economic Impact
Priya Life Science Compound trial record
Compound · clinical trials

Tofacitinib Citrate clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — the 2 trials in our China register that name Tofacitinib Citrate as an intervention. Synced 10 Nov 2026
2Current trials
2Recruiting now
2Lead sponsors
1Country register
At a glance

Tofacitinib Citrate is named as an intervention in 2 current clinical trials in our China register. 2 are recruiting patients now. All registered phases are Phase 2. The sponsor with the most trials is Anhui Provincial Hospital (1). The most-studied condition is Patients With Locally Advanced or Metastatic NSCLC Who Have Failed First-line Immunotherapy.

Where Tofacitinib Citrate is approved

All regulators →

Of the three regulators tracked here, the first to approve Tofacitinib Citrate was the US, on 6 Nov 2012. It is approved in 3 of the 3 regulators tracked here.

USUnited States (FDA)
6 Nov 2012
Xeljanz
NDA203214 on Drugs@FDA
First original NDA/BLA approval
EUEuropean Union (EMA)
22 Mar 2017
Xeljanz
EMA product page
First centralised authorisation
CACanada (Health Canada)
17 Apr 2014
Xeljanz
Notice of Compliance 15510
First new-drug NOC
  • 3 EU safety letters (DHPC), latest: referral - article 20 procedure for Cibinqo / Jyseleca / Olumiant / Rinvoq / Xeljanz, 21 Feb 2023

From the regulators' own registers: FDA Drugs@FDA, the EMA medicines list and Health Canada's Notice of Compliance database. Dates are the first listed approval of a product containing only this substance; combination products and nationally authorised EU medicines are not counted.

Tofacitinib Citrate patents and exclusivity

Expiry tracker →

Protections still running for marketed products containing Tofacitinib Citrate, as listed by the regulators. Expired patents and exclusivities, and discontinued products, are not shown.

US FDA Orange Book Xeljanz, Xeljanz Xr
  • 3 listed patents; the last listed expires 14 Sep 2034 (US 11253523, including a 6-month paediatric extension).
  • Exclusivity PED: Pediatric exclusivity, until 21 Aug 2028.
  • Exclusivity M-14: Other exclusivity: additional clinical trial information added to pediatric use subsection, until 21 Feb 2028.
See the Orange Book listing for NDA 213082
Patents and exclusivities above are pooled across 3 applications for this substance.

Reproduced from the FDA Orange Book and Purple Book (checked 8 Nov 2026) and the European Commission's Union Register of medicinal products (CC BY 4.0; the EU expiry date is calculated exactly as the Commission's register displays it). Listed patents and dates are as submitted to or published by the regulator and may not reflect litigation, invalidation, settlements, lapsed fees or later extensions. This is not legal advice or a freedom-to-operate opinion, and it does not say when a generic or biosimilar will launch.

What health systems spend on Tofacitinib Citrate

All medicines →
ENNHS England
£12
1 items dispensed, Sep 2025 to Aug 2026
-67% on the previous 12 months
Net ingredient cost, community prescriptions
USUS Medicaid
$264.3m
43,863 prescriptions in 2025 · Xeljanz
+3% on 2024
Amount Medicaid reimbursed, before rebates

From NHSBSA Prescription Cost Analysis (Open Government Licence v3.0) and CMS State Drug Utilization Data. Both are gross amounts: neither system publishes its discounts or rebates per drug. Products combining several substances are not counted here.

How Tofacitinib Citrate works

All drug targets →
  • Janus Kinase (JAK) inhibitor Inhibitor
    Target: Janus Kinase (JAK)
    ✓ In ChEMBL and the Guide to Pharmacology
Diseases it has been tested for in clinical trials, by furthest phase
  • COVID-19Phase 3
  • Takayasu arteritisPhase 3
  • Acute respiratory distress syndromePhase 3
  • Alopecia areataPhase 3
  • Alopecia totalisPhase 3
  • Alopecia universalis congenitaPhase 3
  • Ankylosing spondylitisPhase 3
  • Enthesitis-related juvenile idiopathic arthritisPhase 3
  • GlioblastomaPhase 3
  • Granulomatosis with polyangiitisPhase 3
56 diseases in all

Mechanisms and diseases from ChEMBL via the Open Targets Platform (release 26.09), ChEMBL record CHEMBL221959, CC BY-SA 3.0. Targets checked against the IUPHAR/BPS Guide to PHARMACOLOGY (2026.3.1), ligand 5677, CC BY-SA 4.0. Trial phases are not approvals: approved uses are shown from the regulators' own records where we hold them.

NICE appraisals of Tofacitinib Citrate

All NICE appraisals →

NICE, which decides whether the NHS in England should fund new medicines, has published 5 technology appraisals of Tofacitinib Citrate. 5 are current, and 5 of these recommend it for at least some patients.

AppraisalNICE recommendationPublishedStatus
Tofacitinib for treating active ankylosing spondylitis
NICE TA920
Optimised18 Oct 2023Current
Tofacitinib for treating juvenile idiopathic arthritis
NICE TA735
Optimised20 Oct 2021Current
Tofacitinib for moderately to severely active ulcerative colitis
NICE TA547
Recommended28 Nov 2018Current
Tofacitinib for treating active psoriatic arthritis after inadequate response to DMARDs
NICE TA543
Recommended3 Oct 2018Current
Tofacitinib for moderate to severe rheumatoid arthritis
NICE TA480
Optimised11 Oct 2017Current

NICE decisions apply to the NHS in England. In Ireland the HSE decides on reimbursement, advised by the National Centre for Pharmacoeconomics. Titles, categories and dates link to the guidance on nice.org.uk. © NICE 2026 technology appraisal guidance. Available from www.nice.org.uk/guidance. All rights reserved. Subject to Notice of rights. NICE guidance is prepared for the National Health Service in England. All NICE guidance is subject to regular review and may be updated or withdrawn. NICE accepts no responsibility for the use of its content in this product/publication.

Patient leaflets for Tofacitinib Citrate

The package leaflet is the official guide for patients that comes with every medicine. These links go to the regulators that publish it.

  • IE
    Ireland: 8 products on the HPRA list
    Each product record links to the HPRA, which publishes the leaflet and SmPC.
  • EU
    European Union: Xeljanz
    EMA product information: package leaflet and summary of product characteristics in every EU language.
  • UK
    United Kingdom: Search MHRA Products
    Patient information leaflets and SmPCs for UK-licensed products.
  • US
    United States: Search DailyMed
    FDA-approved labels, including patient and medication guides.

Leaflets differ between brands and countries; always read the one that comes with your own medicine. This is regulatory information, not medical advice.

Reference identifiers for Tofacitinib Citrate

ATC code
L04AA29
ChEMBL
CHEMBL221959
DrugBank
DB08895
PubChem CID
9926791
CAS number
477600-75-2
FDA UNII
87LA6FU830
Wikidata
Q3530324
Wikipedia
Tofacitinib

Codes that identify this medicine in other databases, from Wikidata (CC0), matched by its ChEMBL ID. The ATC code is the WHO classification of what the medicine is used for.

Trials by status

  • Recruiting2100%

Trials by phase

  • Phase 22100%
01

Clinical trials of Tofacitinib Citrate

2 trials
StudyPhaseStatusLead sponsorRegisters
A Clinical Trial of TQH3906 Capsules in the Treatment of Active Psoriatic Arthritis
NCT07406035 · ClinicalTrials.gov ↗ · Psoriatic Arthritis
Phase 2 Recruiting Chia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd China
Tislelizumab Combined With Tofacitinib and Docetaxel for NSCLC After Failure of First-Line Immunotherapy
NCT07925866 · ClinicalTrials.gov ↗ · Patients With Locally Advanced or Metastatic NSCLC Who Have Failed First-line Immunotherapy
Phase 2 Recruiting Anhui Provincial Hospital China

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Trial titles and statuses are copied from the registry as published.

02

Conditions studied with Tofacitinib Citrate

2 conditions
Patients With Locally Advanced or Metastatic NSCLC Who Have Failed First-line Immunotherapy1Psoriatic Arthritis1
03

Sponsors

lead sponsor per trial
Lead sponsorTrials
Anhui Provincial Hospital1
Chia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd1
04

By country register

RegisterTrialsRecruiting
Clinical trials in China22

A trial with sites in more than one country appears in each of those registers.

05

Related compounds

06

Questions about Tofacitinib Citrate trials

How many clinical trials are testing Tofacitinib Citrate?

2 current trials in our China register name Tofacitinib Citrate as a drug or biological intervention, as of the registry sync on 10 November 2026. Completed and withdrawn studies are not counted.

Are Tofacitinib Citrate trials recruiting patients?

Yes. 2 of the 2 trials are recruiting: 2 with sites in China. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Who sponsors Tofacitinib Citrate clinical trials?

Anhui Provincial Hospital (1) and Chia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd (1). The number in brackets is how many trials each organisation leads.

Where does this information come from?

Every trial, status, phase and sponsor on this page is copied from public ClinicalTrials.gov records by a daily sync. Nothing here describes how Tofacitinib Citrate works or whether it is effective, and it is not medical advice.

Approvals, shortages and trials, every Friday

One email a week with new EMA and FDA approvals, EU and US medicine shortages, how many trials are recruiting in Ireland, and the week's Irish pharma news.

Free. Unsubscribe from any email with one click. See our privacy policy.

How this page is built

Everything on this page is copied from public ClinicalTrials.gov registry records — it is not written from memory, and nothing here describes how Tofacitinib Citrate works or whether it is effective. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our country trial registers, collects every trial that lists Tofacitinib Citrate (or a registered synonym) as a drug or biological intervention, and tabulates the registry fields directly. Placebos and generic comparators are excluded. There is no AI drafting and no per-compound editorial pass, and the page has not been clinically reviewed. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The ClinicalTrials.gov data on this page was last retrieved on 10 Nov 2026. How every register is built: methodology · fixes we have made: corrections log.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.