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Clinical Trials/NCT00550810
NCT00550810
Unknown
Phase 2

A Phase II Study of SU011248 for Maintenance Therapy in Hormone Refractory Prostate Cancer After First Line Chemotherapy

Alberta Health services4 sites in 1 country30 target enrollmentOctober 2007

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Prostate Cancer
Sponsor
Alberta Health services
Enrollment
30
Locations
4
Primary Endpoint
Progression Free Survival
Last Updated
14 years ago

Overview

Brief Summary

The major goal is to determine whether the experimental agent has clinically promising activity that would merit progression to a formal phase III trial.

Patients with hormone refractory prostate cancer after docetaxel chemotherapy have limited treatment options and no systemic treatment has been proven to be effective. Because of its action, safety and simple administration SU011248 has potential for effectiveness in this disease setting. Promising activity in this study would provide the necessary proof-of-principle for a larger confirmatory study in this population, and potentially in earlier stages of this common disease.

Registry
clinicaltrials.gov
Start Date
October 2007
End Date
November 2012
Last Updated
14 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Male

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Rachel Syme

Dr. Bernie Eigl

Alberta Health services

Eligibility Criteria

Inclusion Criteria

  • Histological or cytological diagnosis of adenocarcinoma of the prostate
  • Metastatic or locally recurrent disease not curable with standard therapy
  • ECOG performance status 0, 1 or 2
  • Prior single agent docetaxel or docetaxel combination chemotherapy with a documented PSA or imaging response, and no objective evidence of disease progression at study enrolment

Exclusion Criteria

  • Patients with a history of other invasive cancer, except adequately treated non
  • melanoma skin cancer.
  • Patients with known brain metastases.
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to SU
  • Other serious intercurrent illness or medical condition that might be aggravated by protocol treatment.

Outcomes

Primary Outcomes

Progression Free Survival

Time Frame: 180 days without evidence of disease progression would be considered clinically worthy of further investigation

Secondary Outcomes

  • -PSA Response -Toxicity(The secondary endpoint of PSA response will also be documented. PSA response is defined as a ≥50% fall in PSA (minimum of 5 µg/L) from baseline maintained for > 3 weeks and without evidence of disease progression otherwise.)

Study Sites (4)

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