drugset / Trial / NCT00277225

A Study to Assess the Pharmacokinetics, Immunogenicity and Safety of Escalating Doses of BMS-188667 Given as a Single Intravenous Infusion to Patients With Psoriasis Vulgaris

NCT00277225

Phase 1 Completed 32 enrolled Bristol-Myers Squibb
RandomizedSingle-groupDouble-blindTreatment

Summary

The purpose of this protocol is to determine the single-dose pharmacokinetics and immunogicity of BMS-188667 administered as a 1 hour intravenous infusion with extended pharmacokinetic sampling. Safety of all subjects will be assessed in a double blind fashion through the inclusion of placebo controls at each dose level.

Timeline

Start
1995-11
Primary completion
1996-06
Completion
1996-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Abatacept Other / unclassified Intravenous

Indications