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Brief Title: A Study Evaluating the Safety, Pharmacokinetics and Anti-Tumor Activity of ABBV-176 in Subjects With Advanced Solid Tumors Likely to Express Prolactin Receptor (PRLR)
Official Title: A Phase 1 Study Evaluating the Safety, Pharmacokinetics and Anti-Tumor Activity of ABBV-176 in Subjects With Advanced Solid Tumors Likely to Express Prolactin Receptor (PRLR)
Study ID: NCT03145909
Brief Summary: This is an open-label, Phase I, dose-escalation study to determine the maximum tolerated dose (MTD) and the recommended phase two dose (RPTD), and to assess the safety, preliminary efficacy, and pharmacokinetic (PK) profile of ABBV-176 for participants with advanced solid tumors likely to express Prolactin Receptor (PRLR). The study will consist of 2 cohorts: Dose Escalation and Expanded Recommended Phase 2 Dose.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
HonorHealth Research Institute - Pima /ID# 161078, Scottsdale, Arizona, United States
City of Hope /ID# 161079, Duarte, California, United States
Yale University /ID# 201357, New Haven, Connecticut, United States
St. Lukes Cancer Institute /ID# 201353, Kansas City, Missouri, United States
Washington University-School of Medicine /ID# 162745, Saint Louis, Missouri, United States
Rutgers Cancer Institute of NJ /ID# 161080, New Brunswick, New Jersey, United States
University of Utah /ID# 161606, Salt Lake City, Utah, United States
Sydney Children's Hospital /ID# 162917, Randwick, New South Wales, Australia
Mater Misericordiae /ID# 162918, South Brisbane, Queensland, Australia
Rigshospitalet /ID# 159707, Copenhagen Ø, Hovedstaden, Denmark
Hosp Univ Madrid Sanchinarro /ID# 161644, Madrid, , Spain
Name: AbbVie Inc.
Affiliation: AbbVie
Role: STUDY_DIRECTOR