The purpose of this study is to determine the maximally tolerated dose and the dose limiting toxicity of this antimitotic, tubulin binding investigational drug for those patients who have failed standard anticancer treatments.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
6
every 3 weeks
Sanofi-Aventis Administrative Office
Bridgewater, New Jersey, United States
Maximal tolerated dose (MTD) and dose limiting toxicity (DLT)
Time frame: Study period
Pharmacokinetic profile, antitumor activity in patients with measurable disease, effect of drug on CYP3A4 activity
Time frame: Study period
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.