Clinical Trials Directory

Trials / Completed

CompletedNCT00394446

Phase 1, Multiple Dose Study of MPC-6827 in Subjects With Refractory Solid Tumors

Phase I Open Label, Dose Escalating, Multiple Dose Study to Determine the Safety, Tolerability, Maximum Tolerated Dose, and Pharmacokinetics of MPC-6827 Administered IV Weekly X 3, Repeated Every 28 Days, in Subjects With Refractory Solid Tumors.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
48 (actual)
Sponsor
Myrexis Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Phase 1, Multiple Dose Study of MPC-6827 in Subjects with Refractory Solid Tumors.

Conditions

Interventions

TypeNameDescription
DRUGMPC-68272-hour intravenous infusion given once weekly for 3 consecutive weeks on a 28 day cycle

Timeline

Start date
2005-03-01
Primary completion
2007-04-01
Completion
2008-02-01
First posted
2006-11-01
Last updated
2008-02-13

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00394446. Inclusion in this directory is not an endorsement.

Phase 1, Multiple Dose Study of MPC-6827 in Subjects With Refractory Solid Tumors (NCT00394446) · Clinical Trials Directory