Continuing Access to Axitinib (A406- AG- 013736 ) For Patients Previously Receiving AG 013736 In Clinical Trials

To allow continuation of axitinib (AG 013736) treatment to patients experiencing clinical benefit in a closing axitinib trial

Patients who were assigned to an axitinib (AG-013736) containing treatment arm in a previous clinical trial
Patients who were receiving axitinib (AG-013736) tablets at the time their previous trial ended
Patients who have stable (SD) or responding disease (PR or CR) documented by the appropriate radiological, clinical, or laboratory assessments within 12 weeks before enrollment (Note: response criteria from the previous axitinib (AG-013736) protocol should be used to determine stable or responding disease).
Patients who have progressive disease (PD) but have experienced "clinical benefit" as defined in the study protocol

Patients may not participate in this trial if the conditions for continuing treatment in the previous axitinib (AG-013736) protocol are not met

Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT00828919.

This is a roll over study aimed to provide continued access to axitinib (monotherapy or

combination, according to treatment received in prior axitinib study) to patients who

have documented stable, or responding disease, or received clinical benefit (as defined

by protocol) at the time of the prior study closure.

Trial PhaseNo phase specified

Trial Typetreatment

Lead OrganizationPfizer Inc

Description