C50
Conditions
Interventions
Group 1: Selected patients on continuing tamoxifen therapy (20 mg per day) who have already participated in the TAMENDOX study (EudraCT no.: 2016-000418-31).
A plasma and a stool sample will be obtain
Sponsors
Robert Bosch Gesellschaft für medizinische Forschung mbH (RBMF)
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Present, signed "Informed Consent Form for the Establishment of a Biomaterial Bank in the TAMENDOX Study". - continuing tamoxifen therapy (20 mg per day) - completed 18th year of age - ability to give consent
Exclusion criteria
Exclusion criteria: - lack of informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| - Plasma concentration of tamoxifen and metabolites - Concentration of tamoxifen and metabolites in stool sample - Composition of the bacterial population in the stool sample | — |
Countries
Germany
Contacts
Public ContactMatthias Schwab
Dr. Margarete Fischer-Bosch - Institut für Klinische Pharmakologie
Outcome results
None listed