A Pilot Study of the Feasibility of Discontinuation of Adalimumab in Stable Rheumatoid Arthritis Patients in Clinical Remission

NCT00808509 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 33

Last updated 2013-12-16

Study results available
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Summary

The purpose of this pilot study is to investigate the possibility of discontinuing adalimumab therapy in patients with rheumatoid arthritis who are in stable remission after treatment with adalimumab in combination with methotrexate.

Conditions

  • Arthritis, Rheumatoid

Interventions

BIOLOGICAL

adalimumab

40 mg every other week via subcutaneous injection

DRUG

methotrexate

At least 10 mg/week administered orally or subcutaneously

Sponsors & Collaborators

  • Pharma Consulting Group AB

    collaborator INDUSTRY
  • AbbVie (prior sponsor, Abbott)

    lead INDUSTRY

Principal Investigators

  • Mikael Heimburger, MD · AbbVie AB

Study Design

Allocation
RANDOMIZED
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-01-31
Primary Completion
2012-09-30
Completion
2012-09-30

Countries

  • Sweden

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00808509 on ClinicalTrials.gov