A Study Evaluating the Safety, Pharmacokinetics, and Anti-tumor Activity of ABBV-321 in Subjects With Advanced Solid Tumors Associated With Overexpression of the Epidermal Growth Factor Receptor (EGFR)

PHASE1CompletedINTERVENTIONAL
Enrollment

62

Participants

Timeline

Start Date

October 10, 2017

Primary Completion Date

April 14, 2021

Study Completion Date

April 14, 2021

Conditions
Advanced Solid Tumors Cancer
Interventions
DRUG

ABBV-321

Intravenous infusion

Trial Locations (18)

2065

Northern Cancer Institute /ID# 166138, St Leonards

3084

Austin Hospital /ID# 166137, Heidelberg

3168

Monash Health /ID# 217435, Clayton

60077

Northshore University Health System Dermatology Clinical Trials Unit /ID# 201095, Skokie

60637

University of Chicago /ID# 166064, Chicago

63110

Washington University-School of Medicine /ID# 214955, St Louis

72762

Highlands Oncology Group /ID# 166132, Springdale

78229

South Texas Accelerated Research Therapeutics /ID# 166134, San Antonio

90025

The Angeles Clinic and Researc /ID# 166133, Los Angeles

95817

University of California, Davis Comprehensive Cancer Center /ID# 215012, Sacramento

5239424

Sheba Medical Center /ID# 166398, Ramat Gan

60611-2927

Northwestern University Feinberg School of Medicine /ID# 165191, Chicago

40536-7001

University of Kentucky Markey Cancer Center /ID# 217665, Lexington

02215

Dana-Farber Cancer Institute /ID# 212920, Boston

10032-3725

Columbia Univ Medical Center /ID# 167184, New York

11794-8183

Stony Brook University Hospital /ID# 216976, Stony Brook

27710-3000

Duke University Medical Center /ID# 166135, Durham

02903-4923

Lifespan Cancer Institute at Rhode Island Hospital /ID# 168600, Providence

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AbbVie

INDUSTRY