Clinical Study With Axitinib In Advanced Kidney Cancer, Who Have Failed First Line Treatment

May 28, 2014 updated by: Pfizer

Clinical Study With Axitinib (AG 013736) In Patients With Metastatic Renal Cell Carcinoma After Failure Of One Prior Systemic First-Line Therapy

This is a single arm study with axitinib in patients with advanced kidney cancer (clear cell variant), who have failed first line therapy. The study will recruit a maximum of 30 patients from 2 countries including Australia and Canada. Patients will be followed up for efficacy, safety and health related outcomes.

Study Overview

Status

No longer available

Conditions

Intervention / Treatment

Study Type

Expanded Access

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Australia
    • Queensland
      • Douglas, Queensland, Australia, 4814
        • Pfizer Investigational Site
    • Tasmania
      • Hobart, Tasmania, Australia, 7000
        • Pfizer Investigational Site
    • Victoria
      • Wendouree, Victoria, Australia, 3355
        • Pfizer Investigational Site
  • Canada
    • Quebec
      • Montreal, Quebec, Canada, H2X 1N8
        • Pfizer Investigational Site

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Metastatic renal cell carcinoma with a component of clear cell subtype.
  • Prior first line systemic therapy
  • At least 1 measurable lesion as per Response Evaluation Criterion in Solid Tumors [RECIST 1.1].
  • Adequate hematology, liver and kidney functions
  • Eastern Cooperative Oncology Group [ECOG] performance status of 0 or 1.
  • Life expectancy of ≥12 weeks.
  • Normotensive or well controlled hypertension (less than/equal to 140/90 mm Hg.)
  • Negative pregnancy test
  • Adequate recovery time from prior systemic therapy, surgery or radiation
  • Willing and able subjects who have signed consent

Exclusion Criteria:

  • More than one prior systemic therapy regimen
  • Major bowel-penetrating surgery <4 weeks
  • Active gastro intestinal bleed in past 3 months
  • Active peptic ulcer disease in the past 6 months
  • Current or anticipated use of potent CYP3A4/5 inhibitors
  • Current or anticipated use of known CYP3A4/5 or CYP1A2 inducers
  • Requirement for therapeutic warfarin or high dose steroids
  • Symptomatic or untreated brain metastases
  • A serious uncontrolled medical disorder or active infection
  • Pregnant or breastfeeding females
  • History of another active malignancy
  • Dementia

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Pfizer

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

March 1, 2012

Primary Completion (Actual)

March 1, 2014

Study Completion (Actual)

March 1, 2014

Study Registration Dates

First Submitted

November 14, 2011

First Submitted That Met QC Criteria

November 14, 2011

First Posted (Estimate)

November 17, 2011

Study Record Updates

Last Update Posted (Estimate)

May 30, 2014

Last Update Submitted That Met QC Criteria

May 28, 2014

Last Verified

May 1, 2014

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • A4061061

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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