BMS-599626 in Patients With Advanced Solid Malignancies

• Status: Completed
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this trial is to identify the highest oral dose of BMS-599626, a drug that is directed against EGFR and HER2 proteins, that can be given safely on a daily schedule of 21 days with a 7 day rest period in patients with cancer who no longer benefit from other commonly used treatments. The study will also test for other proteins that may be affected by BMS-599626; and the level of study drug in the blood will be studied.

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Bristol-Myers Squibb

Criteria

Inclusion Criteria:

• Diagnosis of metastatic cancer that has progressed on currently available therapies;

• At least 3 month life expectancy;

• Primary cancer must be solid (non-hematologic);

• Adequate bone marrow, liver & kidney function;

• Negative pregnancy test.

Exclusion Criteria:

• Serious, uncontrolled medical disorder;

• Individuals not willing or able to use an acceptable method to avoid pregnancy for the entire study period and for at least 3 months after the study;

• Pregnant or breastfeeding women;

• Patients with known brain metastasis;

• Uncontrolled or significant cardiovascular disease;

• Anticancer therapy within 2-6 weeks prior to study drug (depending on the therapy)