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Spots Global Cancer Trial Database for A Study Evaluating the Safety and Pharmacokinetics of ABBV-075 in Subjects With Cancer

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Trial Identification

Brief Title: A Study Evaluating the Safety and Pharmacokinetics of ABBV-075 in Subjects With Cancer

Official Title: A Phase 1 Study Evaluating the Safety and Pharmacokinetics of ABBV-075 in Subjects With Advanced Cancer

Study ID: NCT02391480

Interventions

ABBV-075
Venetoclax

Study Description

Brief Summary: This is a Phase 1, first-in-human, dose escalation study in participants with advanced solid tumors to determine the pharmacokinetics, maximum tolerated dose and the recommended Phase 2 dose of ABBV-075 at different monotherapy dosing schedules. In addition the study will evaluate the safety. tolerability and the pharmacokinetics of ABBV-075 monotherapy or combination therapy in disease specific expansion cohorts.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Scottsdale Healthcare /ID# 132963, Scottsdale, Arizona, United States

City of Hope /ID# 154053, Duarte, California, United States

UC Davis Comp Cancer Ctr /ID# 154644, Sacramento, California, United States

Yale University /ID# 136982, New Haven, Connecticut, United States

University of Chicago /ID# 155453, Chicago, Illinois, United States

Indiana Univ School Medicine /ID# 132946, Indianapolis, Indiana, United States

Duke Univ Med Ctr /ID# 154647, Durham, North Carolina, United States

Mary Crowley Cancer Research /ID# 154059, Dallas, Texas, United States

Univ TX, MD Anderson /ID# 132276, Houston, Texas, United States

UT MD Anderson Cancer Center /ID# 164122, Houston, Texas, United States

Contact Details

Name: AbbVie Inc.

Affiliation: AbbVie

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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