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Safety and Efficacy of Adalimumab in Patients With Moderate to Severely Active Psoriatic Arthritis

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Abbott

Status and phase

Completed
Phase 3

Conditions

Psoriatic Arthritis

Treatments

Biological: Human anti-TNF monoclonal antibody/adalimumab

Study type

Interventional

Funder types

Industry

Identifiers

NCT00195689
M02-537

Details and patient eligibility

About

The purpose of the study is to assess the long-term safety and clinical efficacy of adalimumab in treatment of moderate to severely active psoriatic arthritis

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subject completed study M02-518 or M02-570

Exclusion criteria

  • Subject prematurely discontinued study M02-518 or M02-570

    • Female subject who is pregnant or breast-feeding or considering becoming pregnant
    • Subject considered by the investigator, for any reason, to be an unsuitable candidate for the study

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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