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Effect of Different Doses of AMG 706 on the Gallbladder in Advanced Solid Tumors

Phase 1
Completed
Conditions
Solid Tumors
Interventions
Registration Number
NCT00448786
Lead Sponsor
Amgen
Brief Summary

The study involves the use of three different dosing regimens of AMG 706 in patients with advanced solid tumors to see how the drug affects the gallbladder size and function. The study will be conducted in 11 sites in the US and Australia. A total of 48 patients will be enrolled in the study with the possibility of enrolling 8 more in each treatment arm.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
49
Inclusion Criteria
  • Histologically confirmed advanced metastatic solid tumor
  • Ineligible to receive or progressed on standard of care therapies
  • Measurable or non-measurable disease per modified RECIST
  • Gallbladder must be in situ on screening ultrasound
  • ECOG Performance Status of 0 to 2
  • Life expectancy of 6 months or more as determined by the investigator
  • Adequate organ and hematologic function as evidenced by laboratory studies prior to randomization
  • Men and women 18 years or older
Exclusion Criteria
  • Uncontrolled CNS metastases
  • Known history of prior cholecystitis, prior biliary procedure or prior or ongoing biliary disease
  • Radiation therapy within 14 days prior to randomization
  • Peripheral neuropathy > Grade 1 per CTC AE v.3
  • Currently or previously treated with AMG 706 or other VEGF inhibitors such as SU11248 (sunitinib), PTK787 (vatalanib), AZD2171, BAY 43-9006 (sorafenib), ZD6474 (vandetanib)
  • Previous treatment with bevacizumab is allowed if at least 6 weeks have elapsed from the last dose of bevacizumab to the date of randomization
  • Any anti-coagulant therapy within 7 days prior to randomization; low dose heparin and warfarin for prophylaxis against central venous catheter thrombosis is allowed
  • Less than 30 days have elapsed since participation in an investigational drug/device study or currently receiving investigational treatments
  • History of arterial or venous thrombosis within 1 year prior to randomization
  • History of bleeding diathesis or bleeding within 14 days of randomization
  • MI, CVA, TIA, PTCA/stent, CHF, Grade 2 or greater PVD, uncontrolled arrhythmias or unstable angina within one year prior to randomization
  • Uncontrolled HTN defined by a resting BP of >150/90 mmHg
  • Surgery: major surgical procedure within 4 weeks or 28 days prior to randomization; minor surgical procedure, placement of access device or fine needle aspiration within 7 days of randomization; planned elective surgery while on study
  • Non-healing or open wound, ulcer or fracture
  • Known ongoing or active infection
  • Known (+) for HIV, Hep C or Hep B surface antigen
  • Known chronic hepatitis
  • Known history of allergy or hypersensitivity to AMG 706 or any of its components
  • Pregnant, ie, (+) b-HCG; breastfeeding

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Arm CAMG 706Arm C - AMG 706 75 mg BID 5-days on and 2-days off
Arm BAMG 706Arm B - AMG 706 75 mg BID 2-weeks on and 1-week off
Arm AAMG 706Arm A = AMG 706 125 mg PO daily continuously
Primary Outcome Measures
NameTimeMethod
Average change from baseline in gallbladder size (volume by ultrasound)Anticipated 8 months of treatment with AMG 706
Average change from baseline in gallbladder function (ejection fraction)Subject treatment with AMG 706 anticipated to be 8 months
Secondary Outcome Measures
NameTimeMethod
Average changes from baseline in gallbladder size (volume by CT scan)Subject treatment with AMG 706 anticipated to be 8 months
Maximum change from baseline in gallbladder size (volume) and function (ejection fraction)Subject treatment with AMG 706 anticipated to be 8 months
Change in gallbladder size (volume) and function (ejection fraction) between the last on-treatment measurement and the last available off-treatment measurementSubject treatment with AMG 706 anticipated to be 8 months
Objective response in subjects with measurable disease at baselineSubject treatment with AMG 706 anticipated to be 8 months
Pharmacokinetics of AMG 706 monotherapySubject treatment with AMG 706 anticipated to be 8 months
Subject incidence of treatment-emergent adverse events (including all, serious, grade 3, grade 4 and treatment-relatedSubject treatment with AMG 706 anticipated to be 8 months
Other selected gallbladder characteristics such as size, area, wall thickness, ductal size, presence of stones, pericholecystic fluid and sludgeSubject treatment with AMG 706 anticipated to be 8 months
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