Psoriasis Clinical Trial

Efficacy and Safety of ABT-874 in Subjects With Moderate to Severe Chronic Plaque Psoriasis

Summary

The purpose of the study is to assess the safety and efficacy of ABT-874 in the treatment of moderate to severe chronic plaque psoriasis.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Subject was age 18 or older and in good health (Investigator discretion) with a recent stable medical history.
Subject had a clinical diagnosis of psoriasis for at least 6 months, and had moderate to severe plaque psoriasis

Exclusion Criteria:

Subject had previously received systemic or biologic anti-IL-12 therapy
Subject cannot discontinue systemic therapies and/or topical therapies for the treatment of psoriasis and cannot avoid UVB or PUVA phototherapy
Subject is taking or requires oral or injectable corticosteroids
Subject considered by the investigator, for any reason, to be an unsuitable candidate for the study
Female subject who is pregnant or breast-feeding or considering becoming pregnant

Study is for people with:

Psoriasis

Phase:

Phase 2

Estimated Enrollment:

180

Study ID:

NCT00292396

Recruitment Status:

Completed

Sponsor:

AbbVie (prior sponsor, Abbott)

Check Your Eligibility

Let’s see if you might be eligible for this study.

What is your age and gender ?

Submit

There are 24 Locations for this study

See Locations Near You

Site Reference ID/Investigator# 3351
San Diego California, 92123, United States
Site Reference ID/Investigator# 3347
Alpharetta Georgia, 30022, United States
Site Reference ID/Investigator# 3348
Skokie Illinois, 60077, United States
Site Reference ID/Investigator# 993
Indianapolis Indiana, 46256, United States
Site Reference ID/Investigator# 990
Boston Massachusetts, 02114, United States
Site Reference ID/Investigator# 3349
St. Louis Missouri, 63117, United States
Site Reference ID/Investigator# 992
Cincinnati Ohio, 45219, United States
Site Reference ID/Investigator# 991
Lake Oswego Oregon, 97035, United States
Site Reference ID/Investigator# 3367
Portland Oregon, 97223, United States
Site Reference ID/Investigator# 3346
Johnston Rhode Island, 02919, United States
Site Reference ID/Investigator# 994
Nashville Tennessee, 37215, United States
Site Reference ID/Investigator# 3350
Dallas Texas, 75246, United States
Site Reference ID/Investigator# 796
Houston Texas, 77030, United States
Site Reference ID/Investigator# 2081
Salt Lake City Utah, 84132, United States
Site Reference ID/Investigator# 3366
Norfolk Virginia, 23507, United States
Site Reference ID/Investigator# 989
Seattle Washington, 98101, United States
Site Reference ID/Investigator# 3361
Halifax , B3H 1, Canada
Site Reference ID/Investigator# 985
Laval , H7S 2, Canada
Site Reference ID/Investigator# 987
London , N5X 2, Canada
Site Reference ID/Investigator# 3364
Montreal , H2K 4, Canada
Site Reference ID/Investigator# 794
North Bay , P1B 3, Canada
Site Reference ID/Investigator# 988
Quebec City , G1V 4, Canada
Site Reference ID/Investigator# 795
Waterloo , N2J 1, Canada
Site Reference ID/Investigator# 3360
Windsor , N8W 1, Canada

How clear is this clinincal trial information?

Study is for people with:

Psoriasis

Phase:

Phase 2

Estimated Enrollment:

180

Study ID:

NCT00292396

Recruitment Status:

Completed

Sponsor:


AbbVie (prior sponsor, Abbott)

How clear is this clinincal trial information?

×

Introducing, the Journey Bar

Use this bar to access information about the steps in your cancer journey.

Please confirm you are a US based health care provider:

Yes, I am a health care Provider No, I am not a health care provider