This study will evaluate the safety and efficacy of MCS110 in patients with prostate cancer and bone metastases
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
3
Anti-M-CSF antibody
NV Cancer Institute
Las Vegas, Nevada, United States
CTRC
San Antonio, Texas, United States
Frequency and characteristics of treatment related dose-limiting-toxicities in dose escalation phase
Time frame: every cycle - (cycle = 28 days)
Type and frequency of adverse drug reactions and serious adverse drug reactions
Time frame: every cycle - (cycle = 28 days)
Change in markers of bone resorption and formation (pre- vs. post-treatment)
Time frame: 3 months
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