Clinical Trials Directory

Trials / Completed

CompletedNCT00909688

Study to Evaluate Whether BLI-489 Can be Safely Tolerated by Healthy Subjects Given Multiple Doses

Ascending Multiple Dose Study of the Safety, Tolerability, and Pharmacokinetics of BLI-489 Administered Intravenously to Healthy Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
16 (actual)
Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer · Industry
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

To determine the safety, tolerability, and drug absorption profile of multiple IV doses of BLI 489 in healthy subjects.

Conditions

Interventions

TypeNameDescription
DRUGBLI-489
DRUGplacebo

Timeline

Start date
2009-06-05
Primary completion
2009-07-24
Completion
2009-07-24
First posted
2009-05-28
Last updated
2018-09-27

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00909688. Inclusion in this directory is not an endorsement.