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Multicenter Follow Up Study Of Subjects Who Participated In An Original Protocol Of Exemestane Vs. Megestrol Acetate In Postmenopausal Women With Metastatic Breast Cancer

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Pfizer

Status and phase

Completed
Phase 3

Conditions

Metastatic Breast Cancer

Treatments

Drug: Megestrol acetate
Drug: exemestane (Aromasin)

Study type

Interventional

Funder types

Industry

Identifiers

NCT01237327
971-ONC-0028-094
A5991027

Details and patient eligibility

About

Long term efficacy of exemestane as compared to megestrol acetate in the treatment of women with natural or induced postmenopausal status with advanced breast cancer whose disease has progressed following anti-estrogens or anti-estrogens plus chemotherapy and who had participated on an original study of exemestane vs megestrol : study 971-ONC-0028-080.

Enrollment

84 patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Previous participation in study 971-ONC-0028-080.

Exclusion criteria

  • Subjects who had not previously participated in study 971-ONC-0028-080.

Trial design

84 participants in 2 patient groups

1
Active Comparator group
Treatment:
Drug: Megestrol acetate
2
Experimental group
Treatment:
Drug: exemestane (Aromasin)

Trial contacts and locations

7

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Data sourced from clinicaltrials.gov

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