[No standalone website (unbranded, no questionnaire)] A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness of Adalimumab Introduction Compared With Methotrexate Dose Escalation (CONTROL)

How to apply

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Study’s contact

Call center

+82328506727

Email address

MinJi.Ma@celltrion.com

Condition

Rheumatoid Arthritis

Treatment type

Interventional

Investigational product

CT-P13

Phase

Phase 3

Sponsor

Celltrion

ClinicalTrials.gov identifier

NCT03707535

Study number

CT-P13 3.6

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About the study

To demonstrate that CT-P13 is equivalent to China-approved Remicade at Week 14, in terms of efficacy as determined by clinical response according to the change from baseline in disease activity.

Who can take part?

You may be eligible to participate in the study if you meet the following criteria:

Inclusion criteria

  1. Has a diagnosis of rheumatoid arthritis
  2. Has active disease as defined in DAS28 Criteria
Exclusion criteria

  1. Has a history of tuberculosis (TB) or a current diagnosis of TB
  2. Has previously received a biological agent
  3. Has previously received a tumor necrosis factor alpha (TNF α) inhibitor
  4. Allergies to any of the excipients of infliximab or hypersensitivity to murine and/or human proteins or immunoglobulin products
  5. Pregnant or lactating

For a full list of inclusion/exclusion criteria, please visit ClinicalTrials.gov

Study locations

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How to apply

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