APOLLO(Aromatase inhibitor Patient cOmpLiance program with qoL questionaire) - APOLLO

Study identifier:NIS-OKR-ARI-2007/1

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A prospective observational study of compliance in the patients receiving aromatase inhibitor as an adjuvant therapy in postmenopausal early breast cancer

Medical condition

Breast Cancer

Phase

-

Healthy volunteers

No

Study drug

-

Sex

Female

Actual Enrollment

862

Study type

Observational

Age

18 Years +

Date

Study Start Date: 01 May 2007
Primary Completion Date: 01 Apr 2011
Study Completion Date: 01 Apr 2011

Study design

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

Verification:

Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria