drugset / Trial / NCT00306878

Phase I Study of BMS-188667 (CTLA4Ig) in Patients With Psoriasis Vulgaris

NCT00306878

Phase 1 Completed 45 enrolled Bristol-Myers Squibb
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this clinical research study is to determine the safety, pharmacokinetics, immunogenicity in humans, the recovery time required from the biologic effects and the optimal biologic dose range of BMS188667 (CTLA4Ig)

Timeline

Start
1995-08
Primary completion
1997-05
Completion
1997-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Abatacept Other / unclassified

Indications