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NCT Number: NCT01754935

A Magnetic Resonance Imaging Study and Arthroscopic Biopsy Substudy in Subjects With Active Rheumatoid Arthritis Receiving VX-509, an Oral JAK3 Inhibitor

The current study is designed to evaluate the safety and efficacy, including MRI imaging, across a range of VX-509 doses in subjects with active rheumatoid arthritis (RA) who have had an inadequate response to disease-modifying antirheumatic drugs (DMARDs).

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Vertex Investigational Site, Hillerød, Denmark

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About this study

VX-509 is an oral, selective Janus kinase 3 (JAK3) inhibitor being developed by Vertex. In autoimmune diseases, JAK3 is an essential component of the immune signaling cascade. This cascade ultimately contributes to abnormal immune response that results in chronic inflammation and, in the case of rheumatoid arthritis (RA), irreversible damage to cartilage and bones. Selective inhibition of JAK3 offers a new disease modifying approach to the treatment of RA, and a broad range of other autoimmune diseases.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and female subjects 18 to 65 years of age (inclusive)
  • Diagnosis of RA
  • Swollen joint count of ≥6 out of 66 joints and tender joint count of ≥6 out of 68 joints
  • Seropositivity based on either a positive rheumatoid factor or anti cyclic citrullinated peptide antibody at screening -OR- known erosive disease based on previous X-ray report or erosions detected on screening hand and foot X-ray
  • Baseline CRP level or Westergren erythrocyte sedimentation rate ≥1.2 × upper limit of normal
  • Receiving stable therapy with 1 of the following DMARDs: methotrexate, sulfasalazine, leflunomide, anti-malarial drug, or penicillamine
  • Palpable 2+ synovitis of the wrist or ≥2 MCPs in the MRI-designated hand

Exclusion criteria

  • History or presence of a clinically significant medical disorder other than RA that, in the opinion of the investigator and medical monitor, would pose a risk to subject safety or interfere with the study evaluation, procedures, or completion.
  • Inflammatory, rheumatological disorders other than RA, where arthritis may be a prominent feature
  • Planned surgery during the study
  • History of alcohol or drug abuse, or excessive alcohol consumption
  • History of tuberculosis (TB) infection of any kind (pulmonary or extrapulmonary, active or latent), regardless of history of anti-TB treatment.
  • Pregnant or nursing an infant or with a life partner who is pregnant, nursing, or planning to become pregnant

Treatment and study plan

VX-509

Drug

50 mg oral tablet

VX-509 matching placebo

Drug

0 mg oral tablet

Primary outcomes

  1. Proportion of subjects achieving a ≥20% improvement in disease severity according to the American College of Rheumatology criteria (ACR20), using C reactive protein (CRP) (ACR20 CRP)

    Time frame: Week 12

  2. Change from baseline in Disease Activity Score 28 using CRP (4-component) (DAS28-4[CRP])

    Time frame: Week 12

  3. Change from baseline in OMERACT RAMRIS synovitis score in designated hand wrist

    Time frame: Week 12

  4. Change from baseline in OMERACT RAMRIS bone marrow edema (osteitis) in designated hand wrist

    Time frame: Week 12

  5. Change from baseline in OMERACT RAMRIS erosion score in designated hand wrist

    Time frame: Week 12

Secondary outcomes

  1. Proportion of subjects achieving a ACR50 CRP and ACR70 CRP responses

    Time frame: Week 12

  2. Proportion of subjects with DAS28 CRP <2.6, and those who achieve a remission, moderate response or good response according to the European League Against Rheumatism (EULAR) response criteria

    Time frame: Week 12

  3. ACR hybrid scores

    Time frame: Week 12

  4. Change from baseline in Health Assessment Questionnaire -Disability Index (HAQ-DI)

    Time frame: Week 12

  5. Change from baseline in OMERACT RAMRIS synovitis, bone marrow edema (osteitis), erosion scores

    Time frame: Week 6

  6. PK parameters of VX-509 and its metabolite in plasma (maximum observed concentration [Cmax] and area under the concentration versus time curve [AUC])

    Time frame: Week 12

  7. Safety and tolerability as indicated by adverse events, laboratory tests, electrocardiograms (ECGs) and vital signs

    Time frame: Week 12

  8. Change from baseline in the Physical Function subscale of the 36-item Short Form (SF-36)

    Time frame: Week 12

  9. Change from baseline in the Physical Component and Mental Health Components of the SF-36

    Time frame: Week 12

Sponsors and collaborators

Lead sponsor

Vertex Pharmaceuticals Incorporated

Industry

Registry information

Official study title

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Safety, Pharmacokinetics, and Efficacy of VX-509 Using Magnetic Resonance Imaging and Arthroscopic Biopsies in Subjects With Active Rheumatoid Arthritis on Stable Disease-Modifying Antirheumatic Drugs

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
Dec 21, 2012
Registry last updated
May 19, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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