Mass Balance, Pharmacokinetics and Metabolism Study of Alisertib

Completed · Phase 1

Conditions studied: Advanced Solid Tumors, Lymphoma

In brief

The purpose of this study is to assess the mass balance (i.e. cumulative excretion of total radioactivity \[TRA\] in urine and feces) of alisertib and pharmacokinetic (PK) of alisertib in plasma and urine, and of TRA in plasma and whole blood.

Key facts

Study ID

NCT01714947

Run by

Millennium Pharmaceuticals, Inc.

People needed

3

Starts

2013-01-24

Expected to finish

2013-06-14

Last updated by the study team

2018-10-31

Who can join

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

You may qualify if…

• Each participants must meet all of the following inclusion criteria to be enrolled in the study:
• 18 years or older.
• Histologically or cytologically confirmed metastatic and/or advanced solid tumors or lymphomas for which standard curative or life-prolonging treatment does not exist, or is no longer effective or tolerable.
• Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1.
• Expected survival longer than 3 months from enrollment in the study.
• Radiographically or clinically evaluable tumor.
• Suitable venous access for the conduct of blood sampling.
• Recovered from the reversible effects of prior antineoplastic treatment (with the exception of alopecia and Grade 1 neuropathy).
• Female participants who are postmenopausal for at least 1 year OR are surgically sterile OR if of childbearing potential, agree to practice 2 effective methods of contraception at the same time.
• Male participants who agree to practice effective barrier contraception during the entire study and through 4 months after the last dose of study drug OR agree to abstain from heterosexual intercourse.

You may not qualify if…

• Participants meeting any of the following exclusion criteria are not to be enrolled in the study:
• Female participants who are lactating or have a positive serum pregnancy test.
• Treatment with any investigational products or systemic antineoplastic treatment within 21 days before the first dose of alisertib.
• Medical conditions requiring daily, chronic, or regular use of proton pump inhibitors(PPIs) within 7 days preceding the first dose of alisertib, or H2-receptor antagonists within 24 hours preceding the first dose of alisertib.
• Participants requiring systemic anticoagulation (excluding low-dose aspirin, or low-dose anticoagulation to maintain patency of venous access devices). Low molecular weight heparin, administered as preventive treatment, is allowed if the participant has tolerated treatment with a stable dose and schedule without bleeding complications for more than 1 month.
• Major surgery within the 14 days preceding the first dose of alisertib.
• Infection requiring systemic intravenous (IV) antibiotic therapy within 14 days preceding the first dose of study drug, or other severe infection.
• Life-threatening or uncontrolled medical illness unrelated to cancer.
• Ongoing nausea or vomiting that is Grade 2 or worse in intensity.
• Diarrhea that is Grade 2 or worse in intensity or use of an antimotility agent to control diarrhea to an intensity of Grade 1 or lower level.
• Known GI disease or GI procedures that could interfere with the oral absorption, excretion, or tolerance of alisertib.
• History of urinary and/or fecal incontinence.
• History of uncontrolled sleep apnea syndrome and other conditions that could result in excessive daytime sleepiness such as severe chronic obstructive pulmonary disease.
• Inability to swallow tablets, or inability or unwillingness to avoid taking anything by mouth except for water and prescribed medications for 2 hours before and 1 hour after the first dose of alisertib.
• Inadequate bone marrow or other organ function as specified in study protocol.
• Any cardiovascular condition specified in the study protocol.
• Known or suspected human immunodeficiency virus (HIV) positive or hepatitis B surface antigen-positive status, or known or suspected active hepatitis C infection.
• Inability to comply with study visits and procedures including required inpatient confinement (approximately 11-17 days).
• Please note that there are additional exclusion criteria. The study center will determine if you meet all of the criteria.

Where it is running

• Comprehensive Clinical Development — Tacoma, Washington, United States

Full record on ClinicalTrials.gov

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