A Long Term Safety Study With Atrasentan

NCT00127478 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 166

Last updated 2007-11-29

No results posted yet for this study

Summary

The primary purpose of the study is to evaluate long-term safety and tolerability of atrasentan 10 mg in men with hormone refractory prostate cancer.

Conditions

Interventions

DRUG

Atrasentan

Sponsors & Collaborators

Principal Investigators

  • Gary Gordon, MD · Abbott

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-07-31
Completion
2007-06-30

Countries

  • United States
  • Canada
  • France
  • Netherlands
  • United Kingdom

Study Locations

More Related Trials

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 NCT00127478 on ClinicalTrials.gov