List All Liver Cancer Trials

Liver Cancer

OSI-906 for Advanced Hepatocellular Carcinoma (UW10033)
A Randomized, Placebo-controlled, Double-blinded Phase 2 Study of Second-line Treatment With OSI-906 in Patients With Advanced Hepatocellular Carcinoma (HCC) After Failure of First-line Treatment With Sorafenib
Status Conditions Phase Study ID
Closed Advanced Hepatocellular Carcinoma (HCC) Phase II UW10033

This is a randomized, placebo-controlled, double-blind phase 2 study of OSI-906 or placebo at a continuous 150 mg BID dose. The purpose of this study is to determine if OSI-906 is effective in prolonging the time until disease worsens; in prolonging survival; is effective in stopping the growth or shrinking tumor size; finding most common side effects when given to subjects with liver cancer (hepatocellular carcinoma).

William P. Harris, MD
Seattle Cancer Care Alliance 800-804-8824  
Eligibility Criteria (must meet the following to participate in this study)

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No


Inclusion Criteria:

  • Histologically confirmed diagnosis of advanced HCC. Clinical diagnosis by American Association for the Study of Liver Diseases (AASLD) criteria in cirrhotic patients is acceptable. For patients without cirrhosis histological confirmation is mandatory.
  • Patients must have received at least 1 cycle (21 days) of sorafenib as prior systemic treatment for advanced HCC and had confirmed disease progression or had discontinued due to a drug related toxicity.
  • Patient has only received 1 prior sorafenib-containing systemic therapy for HCC.
  • Patient has received their last dose of sorafenib at least 14 days prior to randomization.
  • Patient has recovered from sorafenib or investigational agent related toxicity to ≤ grade 2.
  • Measurable disease according to RECIST (version 1.1)
  • ECOG PS 0 - 1
  • Age ≥ 18 years
  • Child-Pugh Status A or B(7)
  • Barcelona Clinic Liver Cancer (BCLC) stage B/C
  • Previous local therapy (eg, surgery, radiation therapy, hepatic arterial therapy, chemoembolization, radiofrequency ablation, percutaneous ethanol injection, or cryoablation) is permitted if ≥ 21 days before randomization.
  • Fasting glucose ≤ 150 mg/dL (8.3 mmol/L). Concurrent use of non-insulinotropic oral antihyperglycemic therapy is permitted if the dose has been stable for ≥ 4 weeks at the time of randomization.
  • Following laboratory parameters (determined by laboratory):

    • Platelets ≥ 60 x 10^9/L
    • Hemoglobin ≥ 8.5 g/dL
    • ANC ≥ 1.5 x 10^9/L
    • Potassium within normal limits (supplementation may be used)
    • PTT ≤ 2.3 x ULN
    • Magnesium within normal limits (supplementation may be used)
    • Calcium within normal limits (supplementation may be used)
  • Adequate organ function (for a HCC population):

    • LFT ≤ 5 x ULN
    • Albumin ≥ 2.8 g/dL
    • Total bilirubin ≤ 2.8 mg/dL
    • Creatinine ≤ 1.5 x ULN
    • INR ≤ 2.3
  • Estimated life expectancy ≥ 12 weeks based on an investigator assessment of recent changes in laboratory values, performance status, and other clinical criteria.
  • Patients, both males and females, with reproductive potential (ie, menopausal for less than 1 year and not surgically sterilized) must agree to practice effective contraceptive measures throughout the study. Women of childbearing potential must provide a negative pregnancy test (serum or urine) within 14 days prior to randomization.
  • Patients must provide written informed consent to participate in the study.
  • Prior radiation therapy is permitted provided patients have recovered from the acute, toxic effects of radiotherapy prior to randomization. A minimum of 21 days must have elapsed between the end of radiotherapy and randomization; and
  • Prior surgery is permitted provided that the surgery was done ≤ 28 days prior to randomization and adequate wound healing has occurred prior to randomization.
Exclusions (conditions that would prevent participation in this study)
  • Child-Pugh B (8 - 9) or C
  • Patients who are candidates for potentially curative intervention (ie, surgical resection or transplantation).
  • Type 1 diabetes mellitus or Type 2 diabetes mellitus currently requiring insulinotropic or insulin therapy.
  • Prior IGF-1R therapy
  • Patients requiring interferon
  • Patients with uncontrolled symptomatic ascites.
  • Prior investigational agent within 21 days prior to randomization.
  • History of poorly controlled gastrointestinal disorders that could affect the absorption of study drug (eg, Crohn's disease, ulcerative colitis, etc).
  • History of organ allograft including liver transplant.
  • Malignancy other than HCC within the past 3 years:

    - Exceptions: resected basal cell or squamous cell carcinoma of the skin, cured in situ cervical carcinoma, cured ductal carcinoma in situ of the breast, and/or cured superficial bladder cancer.

  • History (within last 6 months) of significant cardiovascular disease unless the disease is well-controlled. Significant cardiac disease includes second/third degree heart block; clinically significant ischemic heart disease; superior vena cava (SVC) syndrome; poorly controlled hypertension; congestive heart failure of New York Heart Association (NYHA) Class II or worse (slight limitation of physical activity; comfortable at rest, but ordinary physical activity results in fatigue, palpitation, or dyspnea).
  • History of arrhythmia (multifocal premature ventricular contractions [PVCs], bigeminy, trigeminy, ventricular tachycardia, or uncontrolled atrial fibrillation) that is symptomatic or requires treatment (≥ grade 3), left bundle branch block (LBBB), or asymptomatic sustained ventricular tachycardia are not allowed. Patients with atrial fibrillation controlled by medication are not excluded.
  • QTcF interval at screening ≥ 450 msec
  • Use of drugs that have a known risk of causing Torsades de Pointes (TdP) ('Torsades List' on category.cfm)are prohibited within 14 days prior to randomization.
  • Use of the potent CYP1A2 inhibitors ciprofloxacin and fluvoxamine. Other less potent CYP1A2 inhibitors/inducers are not excluded.
  • History of cerebrovascular accident (CVA) within 6 months prior to randomization or that resulted in ongoing neurologic instability.
  • Active infection or serious underlying medical condition (including any type of active seizure disorder within 12 months prior to randomization) that would impair the ability of the patient to receive study drug.
  • History of human immunodeficiency virus (HIV) infection or acquired immune deficiency syndrome (AIDS)-related illness or serious acute or chronic illness.
  • History of any psychiatric or neurologic condition that might impair the patient's ability to understand or to comply with the requirements of the study or to provide informed consent.
  • Pregnant or breast-feeding females.
  • Symptomatic brain metastases that are not stable, require steroids, are potentially life threatening, or that have required radiation within 28 days prior to randomization; and/or
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to study drug.
Last Updated
January 17, 2012
See this trial at
Access protocol and consent forms at Fred Hutchinson Cancer Research Center
Disclaimer: We update this information regularly. However, what you read today may not be completely up to date.

Please remember:
  • Talk to your health care providers first before making decisions about your health care.
  • Whether you are eligible for a research study depends on many things. There are specific requirements to be in research studies. These requirements are different for each study.