To investigate the safety and efficacy of letrozole monotherapy at a dose of 2.5 mg/day in postmenopausal patients with breast cancer, and to determine the blood concentrations of letrozole and hormones.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
31
Novartis Investigative Site
Kashiwa, Chiba, Japan
Novartis Investigative Site
Matsuyama, Ehime, Japan
Novartis Investigative Site
kooriyama, Fukushima, Japan
Safety during treatment
Time frame: Until disease progression or appearance of unacceptable toxicity whichever comes first
Response Rate during treatment
Time frame: Until disease progression or appearance of unacceptable toxicity whichever comes first
Pharmacokinetics measurement at baseline and at every 4 weeks until 28 weeks
Time frame: Maximum 28 weeks after initiate treatment
Plasma estrogens level at baseline and at every 4 weeks until 28 weeks
Time frame: Maximum 28 weeks after initiate treatment
Duration of response
Time frame: From the first date of response confirmed and the last date of response confirmed
Time to progression
Time frame: From the first date of response confirmed and the last date of response confirmed
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Novartis Investigative Site
Maebashi, Gunma, Japan
Novartis Investigative Site
Kurashiki, Okayama-ken, Japan
Novartis Investigative Site
Kitaadachi-gun, Saitama, Japan
Novartis Investigative Site
Bunkyo-ku, Tokyo, Japan
Novartis Investigative Site
Chuo-ku, Tokyo, Japan
Novartis Investigative Site
Shinjuku-ku, Tokyo, Japan
Novartis Investigative Site
Fukushima, Japan
...and 2 more locations