AzTrials
AzTrials

Rheumatoid ArthritisPhase 3OSKIRA - 1NCT01197521

Evaluation of Effectiveness of Two Dosing Regimens of Fostamatinib Compared to Placebo in Patients With Rheumatoid Arthritis (RA) Who Are Taking Methotrexate But Not Responding.

A Phase 3 study testing fostamatinib in people with Rheumatoid Arthritis, run by AstraZeneca at 127 sites in 17 countries.

Completed

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

Official record
Search all trials

Trial summary

The purpose of the study is to evaluate the effectiveness of two dosing regimens of fostamatinib compared to placebo, in patients with rheumatoid arthritis (RA) who are taking methotrexate but not responding. The study will last for 1 year. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Rheumatoid Arthritis
What is being tested?
fostamatinib
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
923 participants
Where
127 sitesin 17 countries
Study dates
Sep 2010to Nov 2012
Phase
Phase 3
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

Who may be able to join

  • Active rheumatoid arthritis (RA) diagnosed after the age of 16
  • Currently taking methotrexate
  • 6 or more swollen joints and 6 or more tender/painful joints (from 28 joint count) and either Erythrocyte Sedimentation Rate (ESR) blood result of 28mm/h or more, or C-Reactive Protein (CRP) blood result of 10mg/L or more
  • At least one of the following: documented history of positive rheumatoid factor (blood test), current presence of rheumatoid factor (blood test), radiographic erosion within 12 months prior to study enrolment, presence of serum anti-cyclic citrullinated peptide antibodies (blood test)

Who cannot join

  • Females who are pregnant or breast feeding
  • Poorly controlled hypertension
  • Liver disease or significant liver function test abnormalities
  • Certain inflammatory conditions (other than rheumatoid arthritis), connective tissue diseases or chronic pain disorders
  • Recent or significant cardiovascular disease
  • Significant active or recent infection including tuberculosis
Show all 9Show fewer
  • Previous failure to respond to a TNF alpha antagonist, anakinra or previous treatment with other biological agent
  • Severe renal impairment
  • Neutropenia

Trial locations and contacts

127 sites in 17 countries.

127 sites in 17 countries

United States41 sites
  • Research Site

    Albany, New York

  • Research Site

    Albuquerque, New Mexico

  • Research Site

    Anniston, Alabama

  • Research Site

    Asheville, North Carolina

  • Research Site

    Atlanta, Georgia

  • Research Site

    Bowling Green, Kentucky

  • Research Site

    Bridgeport, Connecticut

  • Research Site

    Brooklyn, New York

  • Research Site

    Charleston, South Carolina

  • Research Site

    Colorado Springs, Colorado

  • Research Site

    Dallas, Texas

  • Research Site

    Daytona Beach, Florida

  • Research Site

    Erie, Pennsylvania

  • Research Site

    Florissant, Missouri

  • Research Site

    Flowood, Mississippi

  • Research Site

    Greensboro, North Carolina

  • Research Site

    Hixson, Tennessee

  • Research Site

    Houston, Texas

  • Research Site

    Huntington Beach, California

  • Research Site

    Huntsville, Alabama

  • Research Site

    Idaho Falls, Idaho

  • Research Site

    Kalispell, Montana

  • Research Site

    Lake Oswego, Oregon

  • Research Site

    Lewes, Delaware

  • Research Site

    Long Beach, California

  • Research Site

    Marietta, Georgia

  • Research Site

    Memphis, Tennessee

  • Research Site

    Mesquite, Texas

  • Research Site

    Ocala, Florida

  • Research Site

    Olean, New York

  • Research Site

    Perrysburg, Ohio

  • Research Site

    Richmond Heights, Missouri

  • Research Site

    San Antonio, Texas

  • Research Site

    Santa Maria, California

  • Research Site

    Santa Monica, California

  • Research Site

    Springfield, Illinois

  • Research Site

    St Louis, Missouri

  • Research Site

    Tucson, Arizona

  • Research Site

    Tuscaloosa, Alabama

  • Research Site

    Waxford, Pennsylvania

  • Research Site

    Wichita, Kansas

Other trials in United States

India10 sites
  • Research Site

    Ahmedabad, Gujarat

  • Research Site

    Bangalore, Karnataka

  • Research Site

    Hyderabad

  • Research Site

    Kolkata

  • Research Site

    Lucknow, Uttar Pradesh

  • Research Site

    Mangalore, Karnataka

  • Research Site

    Nagpur, Maharshtra

  • Research Site

    Secunderabad, Andhra Pradesh

  • Research Site

    Udupi, Karnataka

  • Research Site

    Visakhapatnam, Andhra Pradesh

Other trials in India

Argentina9 sites
  • Research Site

    Buenos Aires, Buenos Aires F.D.

  • Research Site

    Caba

  • Research Site

    Ciudad Autonoma Bs As, CBA

  • Research Site

    Córdoba, CRD

  • Research Site

    Quilmes

  • Research Site

    Reading, Berkshire

  • Research Site

    Rosario, Santa Fe Province

  • Research Site

    San Juan, San Juan Province

  • Research Site

    San Miguel de Tucumán, TUC

Other trials in Argentina

Ukraine9 sites
  • Research Site

    Donetsk

  • Research Site

    Ivano-Frankivsk

  • Research Site

    Kharkiv

  • Research Site

    Kiev

  • Research Site

    Kyiv

  • Research Site

    Lviv

  • Research Site

    Odesa

  • Research Site

    Vinnytsia

  • Research Site

    Zaporyzhzhya

Other trials in Ukraine

Hungary8 sites
  • Research Site

    Balatonfüred

  • Research Site

    Békéscsaba

  • Research Site

    Budapest

  • Research Site

    Debrecen

  • Research Site

    Makó

  • Research Site

    Sopron

  • Research Site

    Szentes

  • Research Site

    Zalaegerszeg-pozva

Other trials in Hungary

Mexico8 sites
  • Research Site

    Chihuahua City, Chihuahua

  • Research Site

    Guadalajara, Jalisco

  • Research Site

    Mexicali

  • Research Site

    Mexico City, Mexico City

  • Research Site

    Monterrey, Nuevo León

  • Research Site

    Obrergon, Sonora

  • Research Site

    Saltillo, Coahuila

  • Research Site

    San Luis Potosi, Mexico

Other trials in Mexico

Poland8 sites
  • Research Site

    Bytom

  • Research Site

    Chełm Śląski

  • Research Site

    Grodzisk Mazowiecki

  • Research Site

    Katowice

  • Research Site

    Krakow

  • Research Site

    Warsaw

  • Research Site

    Wroclaw

  • Research Site

    Żyrardów

Other trials in Poland

United Kingdom6 sites
  • Research Site

    Christchurch

  • Research Site

    Ipswich

  • Research Site

    London

  • Research Site

    Metropolitan Borough of Wirral

  • Research Site

    Warrington, Cheshire

  • Research Site

    Westcliff-on-the Sea

Other trials in United Kingdom

Brazil5 sites
  • Research Site

    Curitiba, Paraná

  • Research Site

    Recife, Pernambuco

  • Research Site

    Rio de Janeiro

  • Research Site

    São Paulo, São Paulo

  • Research Site

    Vitória, Espírito Santo

Other trials in Brazil

Bulgaria4 sites
  • Research Site

    Plovdiv

  • Research Site

    Sevlievo

  • Research Site

    Sofia

  • Research Site

    Veliko Tarnovo

Other trials in Bulgaria

Slovakia4 sites
  • Research Site

    Bratislava, Slovakia

  • Research Site

    Poprad

  • Research Site

    Rimavská Sobota

  • Research Site

    Žilina, Slovakia

Other trials in Slovakia

Australia3 sites
  • Research Site

    Cairns, Queensland

  • Research Site

    Camperdown, New South Wales

  • Research Site

    Southport, Queensland

Other trials in Australia

Estonia3 sites
  • Research Site

    Pärnu

  • Research Site

    Tallinn

  • Research Site

    Tartu

Other trials in Estonia

Peru3 sites
  • Research Site

    Arequipa, Arequipa

  • Research Site

    Lima, Lima Province

  • Research Site

    Pueblo Libre, Lima region

Other trials in Peru

Belgium2 sites
  • Research Site

    Brussels

  • Research Site

    Yvoir

Other trials in Belgium

Chile2 sites
  • Research Site

    Osorno, Los Lagos Region

  • Research Site

    Santiago

Other trials in Chile

France2 sites
  • Research Site

    Orléans

  • Research Site

    Paris

Other trials in France

About this study

Official title: (OSKIRA-1): A Phase III, Multi-centre, Randomised, Double-Blind, Placebo-Controlled, Parallel Group Study of Two Dosing Regimens of Fostamatinib Disodium in Rheumatoid Arthritis Patients With an Inadequate Response to Methotrexate

The purpose of the study is to evaluate the effectiveness of two dosing regimens of fostamatinib compared to placebo, in patients with rheumatoid arthritis (RA) who are taking methotrexate but not responding. The study will last for 1 year.

Read the detailed description

Sub-study:

Full title: Optional Genetic Research

Date: 18 June 2010

Version: 1

Objectives: To collect and store, with appropriate consent ,DNA samples for future exploratory research into genes/genetic variation that may influence response (ie, absorption, distribution, metabolism and excretion, safety, tolerability and efficacy) to fostamatinib disodium and/or methotrexate; and/or susceptibility to, progression of and prognosis of RA

Being tested
fostamatinib, placebo, fostamatinib
Keywords
Rheumatoid Arthritis
Medical subject headings
Arthritis, Rheumatoid

What participants receive

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

  • fostamatinibDrug

    fostamatinib 100 mg twice daily

  • fostamatinibDrug

    fostamatinib 100 mg twice daily/150 mg once daily

  • placebo, fostamatinibDrug

    Placebo for 24 weeks followed by fostamatinib 100 mg twice daily

Study groups in NCT01197521
Study groupRoleWhat they receive
Dosing Regimen AExperimentalOral Treatment
Receives: Drug: fostamatinib
Dosing Regimen BExperimentalOral Treatment
Receives: Drug: fostamatinib
Dosing Regimen CPlacebo comparatorOral Treatment
Receives: Drug: placebo, fostamatinib

What is being measured

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

  1. Proportion of Patients With ACR20 at Week 24, Comparison Between Fostamatinib and Placebo.

    ACR20: American College of Rheumatology 20% response criteria, based on count of swollen and tender joints (out of 28 joints), blood test measures of inflammation (such as CRP) and the physician and patient's own assessments of disease activity, pain and physical function. Non-responder imputation has been applied by carrying the baseline observation forward. BID=twice daily, CRP=C-reactive protein, DMARD=disease-modifying anti-rheumatic drug, PO=orally, QD=once a day.

    Measured: 24 weeks

  2. Change From Baseline to Week 24 in mTSS, Comparison Between Fostamatinib and Placebo.

    mTSS: modified total Sharp score, a measure of structural progression based upon X-rays. Hand and foot joints are scored for erosions and joint space narrowing and the results summed to give a value between 0 and 448. A higher value represents more serious progression of the disease. After disregarding ineligible records, patients with 2 or more non-missing values have had missing data imputed via linear extrapolation/interpolation methods. Patients with only 1 result have been excluded from the analysis. ANCOVA=analysis of covariance, BID=twice daily, DMARD=disease-modifying anti-rheumatic drug, IP=investigational product, PO=orally, QD=once a day.

    Measured: Baseline and 24 weeks

Secondary outcomes (10)
  1. ACR20 - Proportion of Patients Achieving ACR20, Comparison Between Fostamatinib and Placebo at Week 1

    ACR20: American College of Rheumatology 20% response criteria, based on count of swollen and tender joints (out of 28 joints), blood test measures of inflammation (such as CRP) and the physician and patient's own assessments of disease activity, pain and physical function. Non-responder imputation has been applied by carrying the baseline observation forward. BID=twice daily, CRP=C-reactive protein, DMARD=Disease-modifying anti-rheumatic drug, PO=orally.

    Measured: 1 week

  2. Proportion of Patients Achieving ACR50 up to Week 24

    ACR50: American College of Rheumatology 50% response criteria, based on count of swollen and tender joints (out of 28 joints), blood test measures of inflammation (such as CRP) and the physician and patient's own assessments of disease activity, pain and physical function. Non-responder imputation has been applied by carrying the baseline observation forward. BID=twice daily, CRP=C-reactive protein, DMARD=Disease-modifying anti-rheumatic drug, PO=orally, QD=once a day.

    Measured: 24 weeks

  3. Proportion of Patients Achieving ACR70 up to Week 24

    ACR70: American College of Rheumatology 70% response criteria, based on count of swollen and tender joints (out of 28 joints), blood test measures of inflammation (such as CRP) and the physician and patient's own assessments of disease activity, pain and physical function. Non-responder imputation has been applied by carrying the baseline observation forward. BID=twice daily, CRP=C-reactive protein, DMARD=Disease-modifying anti-rheumatic drug, PO=orally, QD=once a day.

    Measured: 24 weeks

  4. ACRn - Comparison Between Fostamatinib and Placebo at Week 24

    ACRn: American College of Rheumatology index of RA improvement, based on smallest percentage improvement in the count of swollen joints (out of 28 joints), count of tender joints (out of 28 joints), or in blood test measures of inflammation (such as CRP) or the physician or patient's own assessments of disease activity, pain and physical function. Scores are reported as a percentage improvement on a scale of -100 to +100, with larger values representing a better clinical outcome. BID=twice daily, CI=confidence interval, CRP=C-reactive protein, DMARD=Disease-modifying anti-rheumatic drug, PO=orally, QD=once a day, RA=rheumatoid arthritis. Mean refers to change at Week 24.

    Measured: 24 weeks

  5. Proportion of Patients Achieving DAS28-CRP <2.6 at Week 12

    DAS28-CRP: Disease Activity Score based on a count of swollen and tender joints (out of 28 joints), blood test measures of inflammation (CRP) and the patient's own assessment. Scores can take any positive value with a lower value indicating a better clinical condition. A DAS28-CRP score of <2.6 is indicative of remission of RA symptoms. BID=twice daily, CRP=C-reactive protein, DMARD=Disease-modifying anti-rheumatic drug, OR=odds ratio, PO=orally, QD=once a day.

    Measured: 12 weeks

  6. Proportion of Patients Achieving DAS28-CRP <2.6 at Week 24

    DAS28-CRP: Disease Activity Score based on a count of swollen and tender joints (out of 28 joints), blood test measures of inflammation (CRP) and the patient's own assessment. Scores can take any positive value with a lower value indicating a better clinical condition. A DAS28-CRP score of <2.6 is indicative of remission of RA symptoms. BID=twice daily, CRP=C-reactive protein, DMARD=Disease-modifying anti-rheumatic drug, OR=odds ratio, PO=orally, QD=once a day.

    Measured: 24 weeks

  7. Proportion of Patients Achieving DAS28-CRP EULAR Response at Week 24

    Change in DAS28 was derived for each post baseline scheduled assessment and categorised using the European League Against Rheumatism (EULAR) response criteria. Non-responder imputation has been applied by carrying the baseline observation forward. BID=twice daily, CRP=C-reactive protein, DAS28=Disease Activity Score based on a 28-joint count, DMARD=disease-modifying anti-rheumatic drug, OR=odds ratio, PO=orally, QD=once a day.

    Measured: 24 weeks

  8. HAQ-DI Response - Comparison of the Change (>=0.22) From Baseline Between Fostamatinib and Placebo at Week 24

    HAQ-DI: Health Assessment Questionnaire - Disability Index, a measure of physical function. The HAQ-DI score is calculated by summing scores from 8 sub-categories (ie, scores for patient ability in dressing and grooming, rising, eating, walking, hygiene, reach, grip and common daily activities) and dividing by the number of categories completed. The HAQ-DI score takes values between 0 and 3, with higher score indicating greater disability. HAQ-DI response: a reduction from baseline in HAQ-DI greater than or equal to the minimally important difference (0.22). BID=twice daily, DMARD=disease-modifying anti-rheumatic drug, OR=odds ratio, PO=orally, QD=once a day.

    Measured: Baseline and 24 weeks

  9. SF-36 - Comparison of the Change in PCS From Baseline Between Fostamatinib and Placebo at Week 24

    SF-36: 36 item Short Form Health Survey, a measure of health-related QoL. Scores for 8 sub-domains (Physical Functioning, Role-physical, Bodily Pain, General Health, Vitality, Social Function, Role-emotional \& Mental Health) are derived \& normalised to a scale of 0-100. Physical Component Scores (PCS) are derived by multiplying each of these 8 scores by a constant, summing them \& standardising against a population with mean of 50, standard deviation of 10. Higher scores represent a better QoL. Mean changes from baseline score are presented at each visit as increases from baseline (defined as post-baseline minus baseline); larger changes indicate a better clinical condition. ANCOVA=analysis of covariance, BID=twice daily, DMARD=disease modifying antirheumatic drug, PO=orally, QD=once daily, QoL=quality of life.

    Measured: Baseline and 24 weeks

  10. SF-36 - Comparison of the Change in MCS From Baseline Between Fostamatinib and Placebo at Week 24

    SF-36: 36 item Short Form Health Survey, a measure of health-related QoL. Scores for 8 sub-domains (Physical Functioning, Role-physical, Bodily Pain, General Health, Vitality, Social Function, Role-emotional \& Mental Health) are derived \& normalised to a scale of 0-100. Mental Component Scores (MCS) are derived by multiplying each of these 8 scores by a constant, summing them \& standardising against a population with mean of 50, standard deviation of 10. Higher scores represent a better QoL. Mean changes from baseline score are presented at each visit as increases from baseline (defined as post-baseline minus baseline); larger changes indicate a better clinical condition. ANCOVA=analysis of covariance, BID=twice daily, DMARD=disease modifying antirheumatic drug, PO=orally, QD=once daily, QoL=quality of life.

    Measured: Baseline and 24 weeks

Timeline

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

  1. First posted9 Sep 2010 (estimated)
  2. Study startSep 2010
  3. Primary completionNov 2012
  4. Study completionNov 2012

Resources

More details

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

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
923 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01197521
Sponsor's protocol ID
D4300C00001
Other IDs
2010-020743-12
Acronym
OSKIRA - 1
Status last verified
Feb 2014
First submitted
8 Sep 2010
Last updated
7 Apr 2014
Data monitoring committee
Yes

Publications

  • Kjelgaard-Petersen CF, Platt A, Braddock M, Jenkins MA, Musa K, Graham E, Gantzel T, Slynn G, Weinblatt ME, Karsdal MA, Thudium CS, Bay-Jensen AC. Translational Biomarkers and Ex Vivo Models of Joint Tissues as a Tool for Drug Development in Rheumatoid Arthritis. Arthritis Rheumatol. 2018 Sep;70(9):1419-1428. doi: 10.1002/art.40527. Epub 2018 Jul 24.

    PubMed 29669391

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing fostamatinib in people with Rheumatoid Arthritis, run by AstraZeneca at 127 sites in 17 countries.

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 9 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 7 Apr 2014. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 127 sites in United States, India, Argentina, Ukraine, Hungary and 12 more countries. 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. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 7 Apr 2014). 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?

Proportion of Patients With ACR20 at Week 24, Comparison Between Fostamatinib and Placebo. (time frame: 24 weeks). 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 NCT01197521, 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 7 Apr 2014.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in