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AzTrials

Arthritis, RheumatoidESCALATE-RANCT03387423

Observational Study to Determine How Physicians Make Treatment Decisions in Patients Treated With Tofacitinib for Moderate to Severe Active Rheumatoid Arthritis

An observational study of Arthritis, Rheumatoid, run by Pfizer at 91 sites in Germany.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This non-interventional study aims to identify key factors that are driving treatment decisions by rheumatologists in the treatment of rheumatoid arthritis (RA) patients starting treatment with Tofacitinib in a real world setting. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Arthritis, Rheumatoid
What is being tested?
Tofacitinib
How many people
1,459 participants
Where
91 sitesGermany
Study dates
2 Nov 2017to 17 Jul 2023
Phase
Observational
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Adult patients with confirmed diagnosis of rheumatoid arthritis who are eligible for treatment with Tofacitinb according to Summary of Product Characteristics (SmPC)

Who may be able to join

  • Patients aged ≥ 18 years
  • Confirmed Diagnosis of Rheumatoid Arthritis by rheumatologist
  • Patient is eligible for Tofacitinib treatment according to Summary of Product Characteristics (SmPC)
  • Evidence of a personally signed and dated informed consent document indicating that the patient (or a legally acceptable representative) has been informed of all pertinent aspects of the study.

Who cannot join

  • Contraindications according to Xeljanz® SmPC
  • Receipt of any investigational drug within 3 months before study inclusion
  • Patients who have received any previous treatment with Tofacitinib or other JAK inhibitors
  • Patients who are investigational site staff members or patients who are Pfizer employees directly involved in the conduct of the study.

Trial locations and contacts

91 sites in 1 country.

91 sites in 1 country

Germany91 sites
  • Private Practice Kupka

    Altenburg, 04600

  • Private Practise Boehm

    Altenholz, 24161

  • Private Practice Marycz

    Amberg, 92224

  • Private Practice Fuchs

    Augsburg, 86157

  • private practise Gause

    Bad Bramstedt, 24576

  • ACURA Kliniken Rheinland-Pfalz AG

    Bad Kreuznach, 55543

  • MFZ Medizinisches Forschungszentrum Weserbergland

    Bad Pyrmont, 31812

  • Private Practice Manger

    Bamberg, 96047

  • Private Practice Ochs

    Bayreuth, 95444

  • Private Practice Schmitt-Haendle

    Bayreuth, 95444

  • Private Practice

    Bayreuth, 95444

  • Ambulantes Gesundheitszentrum der Charité

    Berlin, 10117

  • Private Practice Bozorg

    Berlin, 10713

  • Private Practice Brandt-Juergens

    Berlin, 12161

  • Privat Practice Remstedt

    Berlin, 12435

  • private practise Herzberg

    Berlin, 12435

  • Private Practice Seifert

    Berlin, 12555

  • Private Practice Zinke

    Berlin, 13055

  • Private Practice Thiele

    Berlin, 14129

  • Immanuel Klinikum Bernau

    Bernau, 16321

  • Private Practise

    Braunschweig, 38100

  • MED Bayern OST GmbH

    Burghausen, 84489

  • Private Practice Lorenz

    Chemnitz, 09139

  • Private Practice Baerlecken

    Cologne, 50996

  • Private Practice Kirrstetter

    Deggendorf, 94469

  • Kreiskranenhaus Demmin GmbH

    Demmin, 17109

  • Private Practice Menne

    Dortmund, 44263

  • Private Practice Luethke

    Dresden, 01097

  • Private Practice Fischer

    Dresden, 01277

  • Private Praxis

    Düsseldorf, North Rhine-Westphalia, 40237

  • private practise Pech

    Eberswalde, 16225

  • Private Practice Steinmueller

    Ehringshausen, 35630

  • Asklepios MVZ Nord SH GmbH, c/o AK St. Georg

    Elmshorn, 25335

  • Private Practice Kaestner

    Erfurt, 99096

  • Private Practice Koch

    Erfurt, 99096

  • Private Practice Haeckel

    Frankenberg, 09669

  • Private Practice Mueller

    Freiberg, 09599

  • SRH Krankenhaus Waltershausen-Friedrichroda GmbH

    Friedrichroda, 99894

  • Private Practice Abahji

    Germering, 82110

  • Private Practice Sensse

    Gifhorn, 38518

  • Private Practice Holst

    Glaisin, 19288

  • Private Practice Zeh

    Göppingen, 73033

  • Private Practice Semmler

    Güstrow, 18273

  • private practise Kühne

    Haldensleben I, 39340

  • Private Practice Liebhaber

    Halle, 06128

  • Private Practice Dahmen

    Hamburg, 22415

  • private practise Aries

    Hamburg, 22767

  • Private Practice Stille

    Hanover, 30161

  • private practise Heilig

    Heidelberg, 69120

  • private practise Wernicke

    Hohen Neuendorf, 16540

  • Private Practice Kremers

    Jülich, 52428

  • Medius Kliniken gGmbH

    Kirchheim unter Teck, 73230

  • Kreiskrankenhaus Langenau

    Langenau, 89129

  • Private Practice Hamann

    Leipzig, 04109

  • Private Practice Schwarze

    Leipzig, 04129

  • Private Practice Kudela

    Magdeburg, 39104

  • private practise Sieburg

    Magdeburg, 39104

  • Private Practice Rossbach

    Mansfeld, 06343

  • Private Practice Harmuth

    Marktredwitz, 95615

  • Private Practice Worsch

    Mühlhausen, 99974

  • Private Practice Krueger

    München, 81541

  • Private Practice Raub

    Münster, 48143

  • Praxis Dr.med. Holger Krauel Facharzt für Innere Medizin und Rheumatologie

    Naumburg, 06618

  • Private Practice Berger

    Naunhof, 04683

  • Private Practise

    Neubrandenburg, 17033

  • Private Practice Volberg

    Neuss, 41462

  • MCN Medic Center Nuernberg GmbH

    Nuremberg, 90443

  • Private Practice Goettl

    Passau, 94032

  • Private Practice Graessler

    Pirna, 01796

  • Private Practice Baumann

    Plauen, 08523

  • Knappschaftsklinikum Soor, Klinik fuer Rheumatologie und Klinische Immunologie

    Püttlingen, 66346

  • Private Practice Wassenberg, Koehler, Weier

    Ratingen, 40878

  • Private Practice Richter

    Rostock, 18059

  • private practise Biewer

    Saarbrücken, 66111

  • MVZ Dialysezentrum Schweinfurt

    Schweinfurt, 97421

  • Private Practice Moebius

    Schwerin, 19053

  • Private Practice

    Schwerin, 19053

  • private practise Ständer

    Schwerin, 19053

  • Private Practice Melzer

    Seesen, 38723

  • MVZ Klinikum Straubing

    Straubing, 94315

  • Private Practice

    Templin, 17268

  • Private Practice Pyra

    Torgelow, 17358

  • Private Practice Haas

    Tübingen, 72072

  • Klinik an der Weissenburg GmbH

    Uhlstaedt-Kirchhasel, 07407

  • Private Practice Rinaldi

    Ulm, 89073

  • Private Practice Woerth

    Wiesbaden, 65189

  • Klinikverbund St. Antonius und St. Josef GmbH

    Wuppertal, 42105

  • Rheuma Praxis Barmen Dres. med. Demirel / Hruschka

    Wuppertal, 42285

  • Private Practice

    Zschopau, Saxony, 09405

  • Private Practice Fricke-Wagner

    Zwickau, 08056

  • Private Practice Alliger

    Zwiesel, 94227

Other trials in Germany

About this study

Official title: ESCALATE-RA A NON-INTERVENTIONAL STUDY OF CRITICAL FACTORS FOR ESCALATING DRUG TREATMENT IN PATIENTS TREATED WITH TOFACITINIB FOR MODERATE TO SEVERE ACTIVE RHEUMATOID ARTHRITIS

This non-interventional study aims to identify key factors that are driving treatment decisions by rheumatologists in the treatment of rheumatoid arthritis (RA) patients starting treatment with Tofacitinib in a real world setting.

Being tested
Tofacitinib
Medical subject headings
Arthritis, Rheumatoid

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • TofacitinibDrug

    Patients who are started on Tofacitinib treatment according to the drug label

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of Participants With Treatment Escalations

    Treatment escalations was defined as participants who switched to another disease modifying antirheumatic drug (DMARD) or combination of DMARDs when compared to the last visit. The following three types of escalations were reported: treatment termination, treatment step-up/switch and treatment step-down. Treatment termination was defined as the termination of a DMARD (or multiple when on combination therapy) without starting a new DMARD therapy. Treatment step-up/switch was defined as an increase from the current treatment regime towards e.g.a combination of DMARDs and treatment step-down, was defined as de-escalation from the current treatment regime, example (e.g.) from combination therapy to monotherapy. One participant can fall into more than 1 type of escalation.

    Measured: From date of first prescription of tofacitinib up to 24 Months

  2. Time to Treatment Escalation

    Time to treatment escalation was defined as time in days from escalation visit date to next escalation visit date. The following three types of escalations were reported: treatment termination, treatment step-up/switch and treatment step-down. Treatment termination was defined as the termination of a DMARD (or multiple when on combination therapy) without starting a new DMARD therapy. Treatment step-up/switch was defined as an increase from the current treatment regime (monotherapy) towards a combination of DMARDs and treatment step-down, was defined as de-escalation from the current treatment regime, e.g. from combination therapy to monotherapy. Number of participants with total number of each type of treatment escalations during the study (step-up/switch, step-down, treatment termination along with all escalations) are reported in this outcome measure.

    Measured: From date of first prescription of tofacitinib up to 24 Months

Secondary outcomes (19)
  1. Time to First Step Up Treatment Escalation

    Time to first step-up treatment escalation was defined for participants who experienced a treatment step-up and was measured as date of first treatment step up escalation minus (-) date of first prescription of tofacitinib. Treatment step-up was defined as an increase from the current treatment regime (monotherapy) towards a combination of DMARDs.

    Measured: From date of first tofacitinib prescription up to date of first step-up treatment escalation (maximum up to 24 months)

  2. Number of Participants Achieving Low Disease Activity (LDA) as Assessed by Simplified Disease Activity Index (SDAI) at Months 3, 6, 9, 12, 15, 18, 21 and 24

    SDAI was calculated using the following formula: SDAI = Tender Joint Count (TJC) (using 28 joints) + Swollen Joint Count (SJC) (using 28 joints) + Patient Global Assessment of Arthritis (PtGA) (0-10 centimetre [cm] scale) + Physician's Global Assessment of Arthritis (PhGA) (0-10 cm scale) + C-reactive protein (CRP) (milligram per decilitre [mg/dL]). TJC28 joints included shoulders, elbows, wrists, metacarpophalangeal (MCP) and proximal interphalangeal (PIP) joints, and knees whereas SJC28 included shoulders, elbows, wrists, MCP, PIP and knees (excluding artificial joints). PtGA and PhGA both were assessed on 0-10 cm visual analogue scale (VAS) scale (0 cm [very well] to 10 cm [worst], where higher scores indicated greater affliction due to disease activity). SDAI total score ranged from 0 to 86, where higher scores indicated higher disease activity. SDAI score of less than or equal to (<=11) indicates LDA.

    Measured: Months 3, 6, 9, 12, 15, 18, 21 and 24

  3. Number of Participants Achieving LDA as Assessed by Clinical Disease Activity Index (CDAI) at Months 3, 6, 9, 12, 15, 18, 21 and 24

    CDAI was calculated using the following formula: CDAI = (28TJC) + (28SJC) + (PhyGA in cm) + (PtGA in cm). TJC28 joints included shoulders, elbows, wrists, MCP and proximal PIP joints, and knees whereas SJC28 included shoulders, elbows, wrists, MCP, PIP and knees (excluding artificial joints). PtGA and PhGA both were assessed on 0-10 cm VAS scale (0 cm [very well] to 10 cm [worst], where higher scores indicated greater affliction due to disease activity). CDAI total score ranged from 0 to 76, where higher scores indicated higher disease activity. CDAI score of <= 10 indicates LDA.

    Measured: Months 3, 6, 9, 12, 15, 18, 21 and 24

  4. Number of Participants Achieving LDA Based on Disease Activity Score (DAS28-4) Erythrocyte Sedimentation Rate (ESR) at Months 3, 6, 9, 12, 15, 18, 21 and 24

    DAS28 is a measure of disease activity in participants with rheumatoid arthritis. DAS28-4 (ESR) was calculated using the following formula: 0.56* square root of (TJC28) + 0.28* square root of (SJC28) + 0.70* natural log (ln) (ESR in [millimeter per hour [mm/ hour]) + 0.014*(PtGA in cm). PtGA was assessed on 0-10 cm VAS scale (scores ranging from 0 cm [very well] to 10 cm [worst]), where higher scores indicated greater affliction due to disease activity). Total DAS28-4 (ESR) score range: 0 (none) to 9.4 (extreme disease activity), higher score indicated more disease activity. DAS28-4 ESR <= 3.2 indicates LDA.

    Measured: Months 3, 6, 9, 12, 15, 18, 21 and 24

  5. Number of Participants Achieving LDA as Based on DAS28-4 C-Reactive Protein (CRP) at Months 3, 6, 9, 12, 15, 18, 21 and 24

    DAS28 is a measure of disease activity in participants with rheumatoid arthritis. DAS28-4 (CRP) was calculated using the following formula: 0.56* square root of (TJC28) + 0.28* square root of (SJC28) + 0.36*ln (CRP in mg/l +1) + 0.014*(PtGA in mm)+ 0.96. PtGA was assessed on 0-10 cm VAS scale (scores ranging from 0 cm [very well] to 10 cm [worst]), where higher scores indicated greater affliction due to disease activity). Total DAS28-4 (CRP) score range: 0 (none) to 9.4 (extreme disease activity), higher score indicated more disease activity. DAS28-4 CRP <= 3.2 indicates LDA.

    Measured: Months 3, 6, 9, 12, 15, 18, 21 and 24

  6. Number of Participants Achieving Remission as Assessed by American College of Rheumatology (ACR)-EULAR Boolean Remission Criteria at Months 3, 6, 9, 12, 15, 18, 21 and 24

    ACR-EULAR Boolean remission criteria was defined as when participant had ACR remission =1 if; TJC28 <=1, SJC28 <=1, CRP <=1mg/dL and PtGA <= 2 cm on a 0 to 10 cm scale, where higher values indicate greater affection due to disease activity.

    Measured: Months 3, 6, 9, 12, 15, 18, 21 and 24

  7. Number of Participants Achieving Remission as Assessed by SDAI at Months 3, 6, 9, 12, 15, 18, 21 and 24

    SDAI was calculated using the following formula: SDAI = (TJC28) + (SJC28) + (PtGA in cm) + (PhGA in cm) + (CRP in mg/dL). TJC28 joints included shoulders, elbows, wrists, MCP and PIP joints, and knees whereas SJC28 included shoulders, elbows, wrists, MCP, PIP and knees (excluding artificial joints). PtGA and PhGA both were assessed on 0-10 cm VAS scale (0 cm [very well] to 10 cm [worst], where higher scores indicated greater affliction due to disease activity). SDAI total score ranged from 0 to 86, where higher scores indicated higher disease activity. SDAI score of <=3.3 indicates remission.

    Measured: Months 3, 6, 9, 12, 15, 18, 21 and 24

  8. Number of Participants Achieving Remission as Assessed by CDAI at Months 3, 6, 9, 12, 15, 18, 21 and 24

    CDAI was calculated using the following formula: CDAI = (28TJC) + (28SJC) + (PhyGA in cm) + (PtGA in cm). TJC28 joints included shoulders, elbows, wrists, MCP and proximal PIP joints, and knees whereas SJC28 included shoulders, elbows, wrists, MCP, PIP and knees (excluding artificial joints). PtGA and PhGA both were assessed on 0-10 cm VAS scale (0 cm [very well] to 10 cm [worst], where higher scores indicated greater affliction due to disease activity). CDAI total score ranged from 0 to 76, where higher scores indicated higher disease activity. CDAI score of <=2.8 indicates remission.

    Measured: Months 3, 6, 9, 12, 15, 18, 21 and 24

  9. Number of Participants Achieving Remission as Assessed by DAS-28 ESR at Months 3, 6, 9, 12, 15, 18, 21 and 24

    DAS28 is a measure of disease activity in participants with rheumatoid arthritis. DAS28-4 (ESR) was calculated using the following formula: 0.56*square root of (TJC28) + 0.28*square root of (SJC28) + 0.70*In (ESR in mm/ hour) + 0.014*PtGA in cm. PtGA was assessed on 0-10 cm VAS scale (scores ranging from 0 cm [very well] to 10 cm [worst]), where higher scores indicated greater affliction due to disease activity). Total DAS28-4 (ESR) score range: 0 (none) to 9.4 (extreme disease activity), higher score indicated more disease activity. DAS28-4 ESR score of <2.6 indicates remission.

    Measured: Months 3, 6, 9, 12, 15, 18, 21 and 24

  10. Number of Participants Achieving Remission as Assessed by DAS28-4 CRP at Months 3, 6, 9, 12, 15, 18, 21 and 24

    DAS28 is a measure of disease activity in participants with rheumatoid arthritis. DAS28-4 (CRP) was calculated using the following formula: 0.56*square root of (TJC28) + 0.28*square root of (SJC28) + 0.36*ln (CRP in mg/l +1) + 0.014*(PtGA in cm)+ 0.96. PtGA was assessed on 0-10 cm VAS scale (scores ranging from 0 cm [very well] to 10 cm [worst]), where higher scores indicated greater affliction due to disease activity). Total DAS28-4 (CRP) score range: 0 (none) to 9.4 (extreme disease activity), higher score indicated more disease activity. DAS28-4 CRP score of <2.6 indicates remission.

    Measured: Months 3, 6, 9, 12, 15, 18, 21 and 24

  11. Change From Baseline in DAS28-4 ESR at Months 3, 6, 9, 12, 15, 18, 21 and 24

    DAS28 is a measure of disease activity in participants with rheumatoid arthritis. DAS28-4 (ESR) was calculated using the following formula: 0.56*square root of (TJC28) + 0.28*square root of (SJC28) + 0.70*In (ESR in mm/ hour) + 0.014*PtGA in cm. PtGA was assessed on 0-10 cm VAS scale (scores ranging from 0 cm [very well] to 10 cm [worst]), where higher scores indicated greater affliction due to disease activity). Total DAS28-4 (ESR) score range: 0 (none) to 9.4 (extreme disease activity), higher score indicated more disease activity.

    Measured: Baseline, Months 3, 6, 9, 12, 15, 18, 21 and 24

  12. Change From Baseline in DAS28-4 CRP at Months 3, 6, 9, 12, 15, 18, 21 and 24

    DAS28 is a measure of disease activity in participants with rheumatoid arthritis. DAS28-4 (CRP) was calculated using the following formula: 0.56*square root of(TJC28) + 0.28*square root of(SJC28) + 0.36*ln (CRP in mg/l +1) + 0.014*(PtGA in cm)+ 0.96. PtGA was assessed on 0-10 cm VAS scale (scores ranging from 0 cm [very well] to 10 cm [worst]), where higher scores indicated greater affliction due to disease activity). Total DAS28-4 (CRP) score range: 0 (none) to 9.4 (extreme disease activity), higher score indicated more disease activity.

    Measured: Baseline, Months 3, 6, 9, 12, 15, 18, 21 and 24

  13. Change From Baseline in Duration of Morning Stiffness at Months 3, 6, 9, 12, 15, 18, 21 and 24

    The duration of morning stiffness was determined by asking the following questions: "When you wake up in the morning, do you currently suffer from morning stiffness?" "How long does the morning stiffness last from the time you wake up?". The change from baseline in duration of morning stiffness was calculated as: morning stiffness at time point -morning stiffness at baseline.

    Measured: Baseline, Months 3, 6, 9, 12, 15, 18, 21 and 24

  14. Change From Baseline in the Functional Ability Questionnaire Hannover (FFbH) at Months 3, 6, 9, 12, 15, 18, 21 and 24

    The FFbH for RA is a German short questionnaire for the assessment of patientive functional capacity in the context of basic everyday activities (range: 0-100% functional capacity, where higher percentage indicates more capacity for everyday activities). The FFbH questionnaire consisted of 18 questions with 3 possible responses (Yes; Yes, but with effort; No or only with outside help). The total score was the sum of the scores of all 18 questions, where for each question (Yes = 2 points; Yes, but with effort = 1 point; No or only with outside help = 0 points).The functional capacity (%) is calculated by (total score*100) divided by (2*number of valid responses). The change from baseline was calculated at each time point as functional capacity at timepoint - functional capacity at baseline.

    Measured: Baseline, Months 3, 6, 9, 12, 15, 18, 21 and 24

  15. Number of Participants Achieving Functional Remission in FFbH at Months 3, 6, 9, 12, 15, 18, 21 and 24

    The FFbH for RA is a German short questionnaire for the assessment of patientive functional capacity in the context of basic everyday activities (range: 0-100% functional capacity, where higher percentage indicates more capacity for everyday activities). The FFbH questionnaire consisted of 18 questions with 3 possible responses (Yes; Yes, but with effort; No or only with outside help). The total score was the sum of the scores of all 18 questions, where for each question (Yes = 2 points; Yes, but with effort = 1 point; No or only with outside help = 0 points). The functional capacity [%] is calculated by (total score*100)/ (2*number of valid responses). Functional remission in FFbH was defined as functional capacity > 83 %.

    Measured: Months 3, 6, 9, 12, 15, 18, 21 and 24

  16. Change From Baseline in European Quality of Life (EuroQoL) Group EuroQoL- 5 Dimensions- 3 Levels (EQ-5D-3L) Total Scores at Months 3, 6, 9, 12, 15, 18, 21 and 24

    The EQ-5D-3L is a standardised instrument used to measure quality of life. It is based on five dimensions: mobility, self-care, usual activities, pain and discomfort, and anxiety and depression with each dimension having three levels of function: 1 indicates no problem; 2 indicates some problem; 3 indicates extreme problem. Scoring formula developed by EuroQol Group (German weights) assigns a utility value for each domain in the profile. Score was transformed and results in a total score range of 0.05 to 1.00; higher scores indicating a better health state.

    Measured: Baseline, Months 3, 6, 9, 12, 15, 18, 21 and 24

  17. Change From Baseline in Functional Assessment of Chronic Illness Therapy (FACIT)- Fatigue Scale at Months 3, 6, 9, 12, 15, 18, 21 and 24

    The FACIT-F Scale is a participant completed questionnaire consisting of 13 items that assess fatigue. Participants responded to each item on a 5-point scale based on their experience of fatigue during the past 7 days (0 = not at all; 1 = a little bit; 2 =somewhat; 3 = quite a bit; 4 = very much). Instrument scoring yielded a range from 0 to 52 (negatively worded items were reversed during analysis), with higher scores representing better participant status (less fatigue).

    Measured: Baseline, Months 3, 6, 9, 12, 15, 18, 21 and 24

  18. Mean Number of Days of Drug Survival at Months 12 and 24

    Drug survival was assessed using Kaplan-Meier methodology. For participants who terminated tofacitinib, the drug survival status was recorded as (status = 1 and time = termination date tofacitinib - date of initiation on tofacitinib) and for participants who do not terminate tofacitinib (status = 0 and time = date of final visit - date of initiation on tofacitinib.

    Measured: At 12 and 24 months

  19. Number of Participants Per Categories of Satisfaction With Tofacitinib Treatment at Months 3, 6, 9, 12, 15, 18, 21 and 24

    Satisfaction with treatment was assessed on a 5-point Likert scale (where 0 = extremely dissatisfied, 1= dissatisfied, 2 = neither satisfied nor dissatisfied, 3 = satisfied and 4 = extremely satisfied) in response to the question "How satisfied are you with the drugs that you have received for your arthritis since your last visit?".

    Measured: Months 3, 6, 9, 12, 15, 18, 21 and 24

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Jan 2018
  2. Study start2 Nov 2017
  3. Primary completion17 Jul 2023
  4. Study completion17 Jul 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
1,459 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03387423
Sponsor's protocol ID
A3921302
Other IDs
ESCALATE-RA
Acronym
ESCALATE-RA
Status last verified
Jul 2024
First submitted
7 Dec 2017
Last updated
21 Oct 2024
Individual data sharing
No: Pfizer will provide access to individual de-identified participant data and related study documents (e.g. protocol, Statistical Analysis Plan (SAP), Clinical Study Report (CSR)) upon request from qualified researchers, and subject to certain criteria, conditions, and exceptions. Further details on Pfizer's data sharing criteria and process for requesting access can be found at: https://www.pfizer.com/science/clinical\_trials/trial\_data\_and\_results/data\_requests.

Publications

  • Krueger K, Behrens F, Brandt-Juergens J, Detert J, Feuchtenberger M, Prothmann U, Behmer O, Hsieh MM, Jobst J, Klaus P, Meng T. Tofacitinib in rheumatoid arthritis: a German real-world study with focus on treatment changes, effectiveness and patient-reported outcomes (ESCALATE-RA). BMJ Open. 2026 Feb 12;16(2):e096952. doi: 10.1136/bmjopen-2024-096952.

    PubMed 41689213

Questions about this trial

What is this clinical trial studying?

An observational study of Arthritis, Rheumatoid, run by Pfizer at 91 sites in Germany.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 21 Oct 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 91 sites in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 21 Oct 2024). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of Participants With Treatment Escalations (time frame: From date of first prescription of tofacitinib up to 24 Months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT03387423, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Oct 2024.

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