A Phase I Study of Oral Ixabepilone in Subjects With Advanced Cancer

Completed · Phase 1

Conditions studied: Cancer

In brief

This study will determine the maximum tolerated dose of oral ixabepilone administered for 5 successive days every 21 days in participants with advanced cancer. The safety, tolerability, and pharmacokinetics of ixabepilone in the body will be studied. In addition, this study will assess preliminary evidence of the effect of food and famotidine on the pharmacokinetics of oral ixabepilone.

Key facts

Study ID

NCT00422097

Run by

R-Pharm

People needed

40

Starts

2007-01-01

Expected to finish

2011-04-01

Last updated by the study team

2016-03-10

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Confirmed diagnosis of solid tumor malignancy unresponsive to current treatment options
• Measurable or nonmeasurable disease as defined by Response Evaluation Criteria in Solid Tumors
• Lapse of at least 1 week since minor surgery and of at least 3 weeks since major surgery and radiation therapy
• Eastern Cooperative Oncology Group performance status of 0-1
• Lapse of at least 4 weeks since immunotherapy or chemotherapy
• Negative pregnancy test result within 72 hours of study drug administration for any woman of childbearing potential (WOCBP)

You may not qualify if…

• WOCBP unable or unwilling to use birth control during study and for up to 4 weeks after study completion
• Women who are pregnant or breastfeeding
• Fertile men not using effective birth control with partners who are WOCBP
• Gastrointestinal(GI) disease or GI tract surgery that could impact drug absorption
• Inability to swallow capsules
• Inability to be venipunctured or to tolerate venous access
• Known symptomatic brain metastases
• Common Terminology Criteria for Adverse Events Grade 2 or greater neuropathy or history of Grade 3 or greater neuropathy
• Psychiatric conditions inhibiting compliance with protocol requirements
• Uncontrolled medical disorder or active infection that would impair participant's ability to receive protocol therapy or whose control may be jeopardized by the study treatment protocol
• Inadequate hematologic, hepatic, or renal function
• History of significant drug allergy
• Previous exposure to ixabepilone
• Exposure to any investigational drug or placebo within 4 weeks of enrollment
• Concurrent chemotherapy regimen
• Use of cytochrome P4503A4 inhibitors or inducers within 2 weeks of treatment initiation (unless approved by medical monitor)
• Use of steroids (except as antiemetic)
• Prisoners or subjects involuntarily detained for treatment

Where it is running

• Georgetown University Medical Center Lombardi Cancer Center — Washington D.C., District of Columbia, United States
• Wayne State University (Hwcrc) — Detroit, Michigan, United States

Full record on ClinicalTrials.gov

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