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OpenTrials
Completed

NCT Number: NCT00081601

Study of CEP-701 in Treatment of Prostate Cancer

The purpose of this study is to determine the proportion of patients with a serological prostate specific antigen (PSA) by day 85.

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Phase 2

Primary location

Johns Hopkins

Baltimore, Maryland, 21287, United States

About this study

A serological PSA response is defined as a reduction from baseline PSA serum concentration of at least 50%, which is confirmed by a second PSA value 28 or more days later.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • at least 18 yrs of age
  • diagnosis of adenocarcinoma of the prostate
  • no detectable metastatic disease as assessed by bone and CT scans
  • has increasing serum PSA concentrations
  • life expectancy of at least 3 months
  • ECOG of 0 or 1
  • has been withdrawn from antiandrogen therapy for at least 6 weeks prior to entering screening period

Exclusion criteria

  • has asymptomatic disease
  • has active GI ulceration or bleeding
  • has been treated with non-hormonal systemic anticancer therapy or has received radiation within 4 weeks of baseline visit
  • bilirubin >2x ULN or ALT or AST >2xULN or serum creatinine >1.5mg/dL
  • hemoglobin <9g/dL or platelets below 100,000/uL or ANC below 1500/uL
  • receiving treatment for HIV with protease inhibitors
  • has had prior malignancy within past 5 yrs with exception of resected basal or squamous cell carcinomas of the skin
  • has used investigational drug with previous one month

Treatment and study plan

CEP-701

Drug

Sponsors and collaborators

Lead sponsor

Cephalon

Industry

Registry information

Official study title

An Open-Label Phase 2 Study of Oral CEP-701 in Patients With Asymptomatic Hormone-Refractory Cancer With Rising Prostate Specific Antigen

Important dates

Study start
2004
Primary completion
2005
Study completion
2005
First posted
Apr 19, 2004
Registry last updated
Aug 24, 2012

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.

Published trials that share one or more normalized conditions with this study.