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An Open-Label Study of SC-005 in Subjects With Triple Negative Breast Cancer (TNBC)
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).
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
University of Chicago /ID# 169231
Chicago, Illinois, United States
Washington University School /ID# 169177
St Louis, Missouri, United States
Memorial Sloan Kettering /ID# 201016
New York, New York, United States
Gabrail Cancer Center Research /ID# 168756
Canton, Ohio, United States
Oklahoma University /ID# 200937
Oklahoma City, Oklahoma, United States
Tennessee Oncology-Sarah Cannon Research Institute /ID# 169233
Nashville, Tennessee, United States
Baylor University /ID# 169860
Houston, Texas, United States
MD Anderson Cancer Center /ID# 169232
Houston, Texas, United States
Start Date
January 4, 2018
Primary Completion Date
October 5, 2018
Completion Date
October 5, 2018
Last Updated
December 17, 2018
2
ACTUAL participants
SC-005
DRUG
Lead Sponsor
AbbVie
NCT05673200
NCT05372640
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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