Clinical Trials Directory

Trials / Terminated

TerminatedNCT00632424

Phase 1 Trial of Oral Ixabepilone

A Phase 1 Study of Ixabepilone Administered as 3 Oral Doses Each Separated by 6 Hours Every 21 Days in Subjects With Advanced Cancer

Status
Terminated
Phase
Phase 1
Study type
Interventional
Enrollment
23 (actual)
Sponsor
R-Pharm · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This Phase 1 study of oral ixabepilone given every 6 hours for 3 doses on Day 1, every 21 days, was a dose-finding study designed to determine the maximum tolerated dose (MTD) and safety of this dosing schedule in participants with advanced cancer

Conditions

Interventions

TypeNameDescription
DRUGIxabepilone (oral formulation)Capsules, Oral, Dose escalating (Phase 1), 3 doses on 1 day every 3 weeks, until disease progression or unacceptable toxicity

Timeline

Start date
2008-05-01
Primary completion
2009-06-01
Completion
2009-06-01
First posted
2008-03-10
Last updated
2016-03-10
Results posted
2010-12-02

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00632424. Inclusion in this directory is not an endorsement.