Sorafenib in Treating Patients With Metastatic or Recurrent Prostate Cancer

NCT00093457 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2023-08-04

No results posted yet for this study

Summary

RATIONALE: Sorafenib may stop the growth of tumor cells by blocking the enzymes necessary for their growth.

PURPOSE: This phase II trial is studying the effectiveness of sorafenib in treating patients who have metastatic or recurrent prostate cancer that has not responded to previous hormone therapy.

Conditions

Interventions

DRUG

sorafenib tosylate

BAY 43-9006 given orally at 400 mg BID in a 28 day cycle

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH
  • NCIC Clinical Trials Group

    lead NETWORK

Principal Investigators

  • Kim N. Chi, MD · British Columbia Cancer Agency

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
120 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-08-10
Primary Completion
2006-09-28
Completion
2011-01-18
FDA Drug
Yes

Countries

  • Canada

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00093457 on ClinicalTrials.gov