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Clinical Trial · NCT03737370
Overview
The objective of this study is to determine the maximum safe dose of Ra-223 in combination with fractionated (split doses) docetaxel when given to subjects and to determine the best administering dose. The study will look at side effects that may happen while taking the combination treatment. A total of approximately 18 subjects will take part in the dose escalation part of the study and an additional 25 subjects will participate in the expansion cohort. This study will be conducted across four centers in the United States.
Sponsor
Tufts Medical Center
Phase
Phase 1
Contacts
Latoya Lashley, MPH
llashley@tuftsmedicalcenter.org
617-636-5409
Christian Lawlor
clawlor3@tuftsmedicalcenter.org
617-636-8897
ClinicalTrials.gov
NCT03737370Drug / Compound
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