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NCT Number: NCT00193154

OSI-774 and Bevacizumab in the Treatment of Patients With Metastatic Renal Cell Carcinoma

In this phase II trial, we plan to evaluate the combination of Tarceva and Avastin in the treatment of patients with metastatic renal cell carcinoma. This trial will be one of the first phase II trials to evaluate a combination of targeted agents in the treatment of a common solid tumor with a strong biologic rationale based on Cancer Biology (VHL/HIF/VEGF/EGFr).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Medical Oncology LLC, Baton Rouge, Louisiana, United States

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About this study

Upon determination of eligibility, all patients will receive:

Tarceva + Avastin

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

To be included in this study, you must meet the following criteria:

  • Metastatic or unresectable clear cell kidney cancer confirmed by biopsy
  • Previous nephrectomy
  • Maximum of 1 previous regimen for metastatic disease
  • Ability to perform activities of daily living with minimal assistance
  • Measurable disease
  • Adequate bone marrow, liver and kidney function
  • Give written informed consent prior to study entry

Exclusion criteria

You cannot participate in this study if any of the following apply to you:

  • Age < 18 years
  • Treatment with more than one previous regimen for metastatic disease
  • Clinically significant cardiovascular disease
  • Active brain metastases
  • History of CNS disease
  • Clinical history of coughing or vomiting blood.
  • History of thromboembolic disease.
  • PEG or G-tube are ineligible.
  • Current use of full dose anticoagulants or thrombolytic agents
  • Chronic daily treatment with aspirin or NSAIDS
  • Any clinical evidence or history of a bleeding or clotting disorder

Please note: There are additional inclusion/exclusion criteria. The study center will determine if you meet all of the criteria. If you do not qualify for the trial, study personnel will explain the reasons. If you do qualify, study personnel will explain the trial in detail and answer any questions you may have.

Treatment and study plan

OSI-774

Drug

150mg PO, days 1-28, cycle repeated every 28 days

Other names: Tarceva

Bevacizumab

Drug

10mg/kg, IV infusion, Days 1 and 15, 28 day cycles

Other names: Avastin

Primary outcomes

  1. Efficacy of the combination of Tarceva and Avastin

    Time frame: 18 months

Secondary outcomes

  1. Objective response rate

    Time frame: 18 months

  2. Progression-free survival

    Time frame: 18 months

  3. Overall Survival

    Time frame: 18 months

  4. Overall tolerability and toxicity of this combination regimen

    Time frame: 18 months

Sponsors and collaborators

Lead sponsor

SCRI Development Innovations, LLC

Other

Collaborators

  • AstraZeneca
  • Genentech, Inc.

Registry information

Official study title

A Phase II Trial of Tarceva (OSI-774) and Avastin (Bevacizumab) in the Treatment of Patients With Metastatic Renal Cell Carcinoma

Important dates

Study start
2003
Primary completion
2004
Study completion
2014
First posted
Sep 19, 2005
Registry last updated
Apr 1, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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