Clinical Trial Detail


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NCT ID NCT03082209
Title A Study of the Safety and Tolerability of ABBV-621 in Participants With Previously Treated Solid Tumors and Hematologic Malignancies
Recruitment Completed
Gender both
Phase Phase I
Variant Requirements No
Sponsors AbbVie
Age Groups: adult | senior
Covered Countries USA | NLD | ESP

Facility Status City State Zip Country Details
Yale University /ID# 158029 New Haven Connecticut 06510 United States Details
The University of Chicago Medical Center /ID# 158030 Chicago Illinois 60637-1443 United States Details
Ingalls Memorial Hosp /ID# 171221 Harvey Illinois 60426 United States Details
Univ Michigan Med Ctr /ID# 207134 Ann Arbor Michigan 48109 United States Details
Rhode Island Hospital /ID# 171157 Providence Rhode Island 02903 United States Details
Vanderbilt University Medical Center /ID# 215000 Nashville Tennessee 37232-0011 United States Details
MD Anderson Cancer Center /ID# 202187 Houston Texas 77030 United States Details
Millennium Oncology /ID# 214981 Houston Texas 77090-1243 United States Details
South Texas Accelerated Research Therapeutics /ID# 160574 San Antonio Texas 78229 United States Details
Medical College of Wisconsin /ID# 171152 Milwaukee Wisconsin 53226-3522 United States Details
National Cancer Center Hospital East /ID# 160596 Kashiwa-shi Chiba 277-8577 Japan Details
Yamagata University Hospital /ID# 200681 Yamagata-shi Yamagata 990-9585 Japan Details
Erasmus Medisch Centrum /ID# 160869 Rotterdam Zuid-Holland 3015 GD Netherlands Details
Universitair Medisch Centrum Groningen /ID# 169748 Groningen 9713 GZ Netherlands Details
Maastricht Universitair Medisch Centrum /ID# 214935 Maastricht 6229 HX Netherlands Details
Universitair Medisch Centrum Utrecht /ID# 169747 Utrecht 3584 CX Netherlands Details
Hospital Universitario Vall d'Hebron /ID# 170809 Barcelona 08035 Spain Details
Hospital Universitario Fundacion Jimenez Diaz /ID# 200106 Madrid 28040 Spain Details
Hospital Universitario HM Sanchinarro /ID# 165136 Madrid 28050 Spain Details
*Shaded cells indicate that there was no data available from for the field