SC-004 Alone or With ABBV-181 in Subjects With Epithelial Ovarian, Fallopian Tube, Primary Peritoneal and Endometrial Cancers
Study Identifier
M16-553
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
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Study Details
Medical Condition
Study Drug
Phase
Phase 1
Sex
Female
Age
18+ years
Protocol Summary
This is a two-part study consisting of Part A (dose regimen finding) followed by Part B (dose expansion). Part A (dose regimen finding) will allow definition of the maximum tolerated dose (MTD) through dose escalation and possible dose interval modification. In Part B (dose expansion), potential therapeutic doses may be studied with SC-004 as monotherapy and SC-004 in combination with ABBV-181 in disease-specific cohorts.
Study Locations
Location
Status
Location
University of Alabama /ID# 202249
Birmingham, Alabama, United States, 35294
Status
Not applicable
Location
Highlands Oncology Group /ID# 209165
Fayetteville, Arkansas, United States, 72703-4005
Status
Not applicable
Location
City of Hope /ID# 202493
Duarte, California, United States, 91010
Status
Not applicable
Location
University of Chicago /ID# 200735
Chicago, Illinois, United States, 60637
Status
Not applicable
Location
Henry Ford Health System /ID# 202480
Detroit, Michigan, United States, 48202
Status
Not applicable
Location
Mayo Clinic - Rochester /ID# 200732
Rochester, Minnesota, United States, 55905-0001
Status
Not applicable
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