Trials / Completed
CompletedNCT01127295
Pharmacology of Adjuvant Hormonotherapy in Breast Cancer
Breast Cancer Adjuvant Hormonotherapy : Tamoxifen and the Anti-aromatases Pharmacokinetics, Correlation With the Pharmacogenetic Characteristics PHACS Protocol : Pharmacology of Adjuvant Hormonotherapy in Breast Cancer
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 2,000 (actual)
- Sponsor
- Institut Claudius Regaud · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is a biomedical study of interventional type, multicenter, inter-regional. Patients with hormono-depending breast cancer, for which an indication of adjuvant hormonotherapy treatment (according to the current treatments) was retained, will be enrolled in this study. The main objective is to estimate the correlations between pharmacokinetic and pharmacogenetic parameters of adjuvant hormonal breast cancer treatment, during the first 3 years.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Tamoxifen, Letrozole, Anastrozole or Exemestane | Tamoxifen 20 mg/day during 5 years Létrozole 2.5 mg/day during 5 years Anastrozole 1 mg/day during 5 years Exémestane 25 mg/day during 5 years |
Timeline
- Start date
- 2010-06-17
- Primary completion
- 2017-12-01
- Completion
- 2017-12-01
- First posted
- 2010-05-20
- Last updated
- 2026-04-14
Locations
24 sites across 1 country: France
Source: ClinicalTrials.gov record NCT01127295. Inclusion in this directory is not an endorsement.