A Study of SC-005 in Subjects With Triple Negative Breast Cancer (TNBC)
Study Identifier
M16-735
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact
Study Details
Medical Condition
Study Drug
Phase
Phase 1
Sex
Female & Male
Age
18+ years
Protocol Summary
This is a multicenter, open-label study in participants with triple negative breast cancer (TNBC) to study the safety, tolerability, pharmacokinetics and preliminary efficacy of SC-005. This study consists of 2 parts: Part A (dose regimen finding) followed by Part B (dose expansion).
Study Locations
Location
Status
Location
University of Chicago /ID# 169231
Chicago, Illinois, United States, 60637-1443
Status
Not applicable
Location
Washington University School /ID# 169177
St Louis, Missouri, United States, 63108
Status
Not applicable
Location
Memorial Sloan Kettering /ID# 201016
New York, New York, United States, 10065
Status
Not applicable
Location
Gabrail Cancer Center Research /ID# 168756
Canton, Ohio, United States, 44718
Status
Not applicable
Location
Oklahoma University /ID# 200937
Oklahoma City, Oklahoma, United States, 73104
Status
Not applicable
Location
Tennessee Oncology-Sarah Cannon Research Institute /ID# 169233
Nashville, Tennessee, United States, 37203
Status
Not applicable
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