Psoriasis Clinical Trial

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Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Doses of AbGn-168 in Psoriasis

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Summary

The general aim of the trial is to determine the safety, tolerability and pharmacologic profile of single escalating doses of AbGn-168 administered subcutaneously or intravenously to patients with chronic plaque psoriasis

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Eligibility Criteria

Inclusion criteria:

Patients with chronic plaque psoriasis covering at least 3% of body surface area. Female subjects must be postmenopausal or surgically sterilized.

Exclusion criteria:

Recent use of biologic agents, oral psoriasis medications or phototherapy

Study is for people with:

Psoriasis

Phase:

Phase 1

Estimated Enrollment:

40

Study ID:

NCT00848055

Recruitment Status:

Completed

Sponsor:

Boehringer Ingelheim

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There is 1 Location for this study

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1240.1.05 Boehringer Ingelheim Investigational Site
Boise Idaho, , United States
1240.1.06 Boehringer Ingelheim Investigational Site
Evansville Indiana, , United States
1240.1.04 Boehringer Ingelheim Investigational Site
Baltimore Maryland, , United States
1240.1.02 Boehringer Ingelheim Investigational Site
Boston Massachusetts, , United States
1240.1.01 Boehringer Ingelheim Investigational Site
New York New York, , United States
1240.1.03 Boehringer Ingelheim Investigational Site
Dallas Texas, , United States
1240.1.7 Boehringer Ingelheim Investigational Site
Berlin , , Germany

How clear is this clinincal trial information?

Study is for people with:

Psoriasis

Phase:

Phase 1

Estimated Enrollment:

40

Study ID:

NCT00848055

Recruitment Status:

Completed

Sponsor:


Boehringer Ingelheim

How clear is this clinincal trial information?

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