Pharmacokinetic Study To Evaluate Effect of Food and Diurnal Variation on ABT-869

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00733187
Recruitment Status : Completed
First Posted : August 12, 2008
Last Update Posted : November 21, 2017
Genentech, Inc.
Information provided by (Responsible Party):
AbbVie ( AbbVie (prior sponsor, Abbott) )

Brief Summary:
To estimate the effect of food on the oral bioavailability and effect of diurnal variation on the pharmacokinetics of ABT-869.

Condition or disease Intervention/treatment Phase
Advanced Solid Tumors Drug: ABT-869 Phase 1

Detailed Description:
This study is a pharmacokinetic study designed to evaluate the effect of food on the oral bioavailability and effect of diurnal variation on the pharmacokinetics of ABT-869. Triplicate ECG performed to determine the effect of ABT-869 on QT prolongation . Subjects may continue receiving linifanib after completion of the study.

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 34 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Basic Science
Official Title: A Pharmacokinetic Study to Evaluate the Effect of Food on the Oral Bioavailability and Effect of Diurnal Variation on the Pharmacokinetics of ABT-869
Study Start Date : February 2009
Actual Primary Completion Date : June 2012
Actual Study Completion Date : June 2012

Arm Intervention/treatment
Experimental: 1 Drug: ABT-869
0.25 mg/kg

Primary Outcome Measures :
  1. Pharmacokinetic [ Time Frame: Various timepoints ]
    Blood samples for the pharmacokinetics of linifanib will be collected for each subject and each regimen (fasting, fed, AM and PM dosings).

  2. ECG Evaluation [ Time Frame: Various timepoints ]
    Triplicate ECG will be performed at designated timepoints.

  3. Adverse Events [ Time Frame: Throught the study ]
    Only treatment emergent AEs will be included. Toxicity grade, relationship to study drug and AEs leading to discontinuation will be evaluated.

  4. Lab data and vital signs [ Time Frame: Various timepoints ]
    Blood chemistry and hematology will be analyzed based on the regimen and dosing and overall. 24 hr ABPM will be analyzed by regimen and dosing time and overall.

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Ages Eligible for Study:   18 Years to 99 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Male or female and age is ≥ 18 years.
  • Must have a histologically or cytologically confirmed non-hematologic malignancy that is refractory to standard therapies or for which a standard effective therapy does not exist.
  • Has measurable or evaluable disease.
  • Eastern Cooperative Oncology Group (ECOG) Performance Score of 0-2.
  • Must have adequate bone marrow, renal and hepatic function as follows:

    • Bone Marrow: Absolute neutrophil count (ANC) ≥ 1,500/mm³; Platelets ≥ 100,000/mm³; Hemoglobin ≥ 9.0 g/dL (1.4 mmol/L)
    • Renal function: serum creatinine ≤ 2.0 mg/dL (0.81 mmol/L);
    • Hepatic function: AST and ALT ≤ 1.5 × ULN unless liver metastases are present, then AST and ALT ≤ 5.0 × ULN; bilirubin ≤ 1.5 mg/dL (0.026 mmol/L)
  • Must have PTT ≤ 1.5 × ULN and/or INR ≤ 1.5 .
  • Women of childbearing potential and men must agree to use adequate contraception (one of the following listed below) prior to study entry, for the duration of study participation and up to two months following completion of therapy. Women of childbearing potential must have a negative urine pregnancy test within 7 days prior to initiation of treatment and/or post menopausal women must be amenorrheic for at least 12 months to be considered of non-childbearing potential.

    • total abstinence from sexual intercourse (minimum one complete menstrual cycle);
    • a vasectomized partner;
    • hormonal contraceptives (oral, parenteral or transdermal) for at least 3 months prior to study drug administration;
    • intrauterine device; * double-barrier method (condoms, contraceptive sponge, diaphragm or vaginal ring with spermicidal jellies or cream)
  • Is capable of understanding and complying with parameters as outlined in the protocol and able to sign the informed consent.
  • Must voluntarily sign and date each informed consent, approved by an Independent Ethics Committee (IEC)/Institutional Review Board (IRB), prior to the initiation of any screening or study-specific procedures.

Exclusion Criteria:

  • Has received anti-cancer therapy within 21 days or within a period defined by 5 half lives, whichever is shorter, prior to study drug administration. Has not recovered to less than or equal to Grade 1 clinically significant adverse effects/toxicities of the previous therapy. Avastin must not have been used less than 60 days prior to receiving ABT-869.
  • Has had major surgery within 21 days of Study Day 1.
  • Has untreated brain or meningeal metastases. Subjects with treated, stable, asymptomatic central nervous system lesions may be considered. Subject must have had stable disease for at least 4 weeks prior to study entry.
  • Has been diagnosed with hepatocellular carcinoma.
  • Pregnant or breastfeeding female.
  • Is receiving therapeutic anticoagulation therapy. Low dose anticoagulation for catheter prophylaxis will be permitted.
  • Has a history of/or currently exhibits clinically significant cancer related events of bleeding. The subject has a recent history of (within 4 weeks of Study Day 1) or currently exhibits other clinically significant signs of bleeding.
  • Has proteinuria CTC Grade > 1 at baseline as measured by a UPC ratio of > 1 and confirmed by a 24 hour urine collection. . Currently exhibits symptomatic or persistent, uncontrolled hypertension defined as diastolic blood pressure (BP) > 100 mmHg; or systolic blood pressure (BP) > 150 mmHg.
  • Has a history of myocardial infarction within 6 months of Study Day 1.
  • Has known autoimmune disease with renal involvement.
  • Is receiving combination anti-retroviral therapy for human immunodeficiency virus (HIV).
  • Clinically significant uncontrolled condition(s).
  • Has active ulcerative colitis, Crohn's disease or celiac disease.
  • LV Ejection Fraction < 50%.
  • Current or previous enrollment in another clinical study.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00733187

Sponsors and Collaborators
AbbVie (prior sponsor, Abbott)
Genentech, Inc.
Study Director: Justin Ricker, MD AbbVie