A multicentre, randomised, comparative trial to assess the tolerance (maximum well-tolerated dose), efficacy and pharmacokinetics of escalating doses of CASODEX (300 mg po daily, increasing by 150 mg intervals) versus castration (medical or surgical) in the treatment of advanced carcinoma of the prostate

Study identifier:7054IL/0009

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A multicentre, randomised, comparative trial to assess the tolerance (maximum well-tolerated dose), efficacy and pharmacokinetics of escalating doses of CASODEX (300 mg po daily, increasing by 150 mg intervals) versus castration (medical or surgical) in the treatment of advanced carcinoma of the prostate

Medical condition

prostate cancer

Phase

Phase 3

Healthy volunteers

-

Study drug

-

Sex

-

Actual Enrollment

-

Study type

Interventional

Age

-

Date

Study Start Date: 01 Nov 1994
Primary Completion Date: -
Study Completion Date: -

Study design

Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -

Verification:

Verified 01 Nov 2013 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria