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

Completed · Phase 1

Conditions studied: Cancer, Breast Cancer, Non-Small Cell Lung Cancer, Acute Myeloid Leukemia (AML), Multiple Myeloma, Prostate Cancer, Small Cell Lung Cancer, Non-Hodgkins Lymphoma

In brief

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.

Key facts

Study ID

NCT02391480

Run by

AbbVie

People needed

128

Starts

2015-04-14

Expected to finish

2019-07-05

Last updated by the study team

2019-11-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participant in the dose escalation cohorts must have histological confirmation of locally advanced or metastatic solid tumor that is either refractory after standard of care therapy for the disease or for which standard of care therapy or does not exist.
• Participants in the expansion cohorts must have histological confirmation of AML, Multiple Myeloma, breast cancer, NSCLC, prostate cancer, SCLC, or NHL that is either refractory after standard of care therapy or for which standard of care therapy does not exist.
• Participant must have an Eastern Cooperative Oncology Group (ECOG) Performance status of: 0 - 1 (dose escalation cohorts) or 0 - 2 (expansion cohorts)
• Participants in the dose escalation cohort must have a serum albumin of ≥ 3.2 g/dL at screening.
• Adequate bone marrow, renal, and hepatic function.
• QTc interval < 480 milliseconds (msec) on the baseline electrocardiogram.

You may not qualify if…

• Participant has untreated brain or meningeal metastases.
• Participant has received anti-cancer therapy including chemotherapy, immunotherapy, biologic or any investigational therapy within a period of 21 days prior to Study Day 1.
• Participant has active peptic ulcer disease or other hemorrhagic esophagitis/gastritis.
• Symptoms of gross hematuria or gross hemoptysis.
• Exhibits symptomatic or persistent, uncontrolled hypertension (BP > or = to 140 and/or diastolic pressure of > or = to 90 mm Hg).
• History of long QT syndrome.
• Peripheral neuropathy greater than or equal to grade 2.

Where it is running

• 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

Full record on ClinicalTrials.gov

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