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
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Study Details

Medical Condition
  • Breast Cancer
  • Study Drug
  • SC-005
  • 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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