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)

PHASE1TerminatedINTERVENTIONAL
Enrollment

19

Participants

Timeline

Start Date

July 3, 2017

Primary Completion Date

November 27, 2018

Study Completion Date

November 27, 2018

Conditions
Advanced Solid Tumors Cancer
Interventions
DRUG

ABBV-176

Intravenous infusion

Trial Locations (11)

2031

Sydney Children's Hospital /ID# 162917, Randwick

2100

Rigshospitalet /ID# 159707, Copenhagen Ø

4101

Mater Misericordiae /ID# 162918, South Brisbane

28050

Hosp Univ Madrid Sanchinarro /ID# 161644, Madrid

63110

Washington University-School of Medicine /ID# 162745, St Louis

91010

City of Hope /ID# 161079, Duarte

85258-2345

HonorHealth Research Institute - Pima /ID# 161078, Scottsdale

06510

Yale University /ID# 201357, New Haven

64111-5905

St. Lukes Cancer Institute /ID# 201353, Kansas City

08903

Rutgers Cancer Institute of NJ /ID# 161080, New Brunswick

84112-5500

University of Utah /ID# 161606, Salt Lake City

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AbbVie

INDUSTRY