Status and phase
Conditions
Treatments
About
The goal of this study is to determine whether a significant pharmacokinetic interaction exists between rapamycin and sorafenib.
This study will also look at the toxicity of the combination of rapamycin and sorafenib and the antitumor activity of the combination in subjects with advanced cancers.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Solid cancer for which curative measures have failed or for which there is no known superior treatment
ECOG performance status 0-2
Measurable or non-measurable disease
Life expectancy of greater than 12 weeks and no anticipated need for other antineoplastic therapy in the next 4 weeks
Age 18 years or older
Patients must have adequate organ and marrow function as defined below:
Women of childbearing potential must have a negative pregnancy test within 7 days of the start of treatment.
Ability to understand and the willingness to sign a written informed consent document
Must not have any evidence of bleeding diathesis.
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
34 participants in 4 patient groups
Loading...
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal