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Brief Title: A Study to Assess Safety and Efficacy of Venetoclax in Combination With Gilteritinib in Participants With Relapsed/Refractory Acute Myeloid Leukemia
Official Title: A Multicenter, Open-Label Phase 1b Study to Assess Safety and Efficacy of Venetoclax in Combination With Gilteritinib in Subjects With Relapsed/Refractory Acute Myeloid Leukemia
Study ID: NCT03625505
Brief Summary: A dose-escalation study evaluating the safety, tolerability, pharmacokinetics (PK) and efficacy of venetoclax, in combination with gilteritinib, in participants with relapsed or refractory (R/R) acute myeloid leukemia (AML) who have failed to respond to, and/or have relapsed or progressed after at least 1 prior therapy.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
David Geffen School of Medicin /ID# 200166, Los Angeles, California, United States
UC San Francisco Medical Center-Parnassus /ID# 200205, San Francisco, California, United States
Sylvester Comprehensive Cancer /ID# 200268, Miami, Florida, United States
Northwestern Memorial Hospital /ID# 200230, Chicago, Illinois, United States
Norton Cancer Institute /ID# 200623, Louisville, Kentucky, United States
Johns Hopkins University /ID# 200349, Baltimore, Maryland, United States
Mayo Clinic - Rochester /ID# 200346, Rochester, Minnesota, United States
Hackensack Univ Med Ctr /ID# 200229, Hackensack, New Jersey, United States
Weill Cornell Medical College /ID# 200109, New York, New York, United States
Hosp of the Univ of Penn /ID# 200348, Philadelphia, Pennsylvania, United States
MD Anderson Cancer Center at Texas Medical Center /ID# 206686, Houston, Texas, United States
Name: ABBVIE INC.
Affiliation: AbbVie
Role: STUDY_DIRECTOR