drugset / Trial / NCT00447681

Study of the Safety, Tolerability, Pharmacokinetics and Pharmcodynamics of ILV-094 in Healthy Subjects

NCT00447681 ↗

Phase 1 Completed 56 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
RandomizedSingle-groupDouble-blindTreatment

Summary

This a randomized, double-blind placebo-controlled inpatient/outpatient, sequential group study of ascending single IV doses of ILV-094, an investigational drug, administered to healthy subjects. In addition, there will be one sub-cutaneous dose cohort, which will follow the 25 mg IV dose.

Timeline

Start
2006-12
Primary completion
—
Completion
2007-11

Drugs

EvaluationDrugModalityDoseRoute
Subject FEZAKINUMAB Monoclonal antibody 25 mg Intravenous

Indications

No indication recorded.