Finding studies
Finding studies
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Clinical Trials Referral Office
CONTACT
Cancer Center Clinical Trials
CONTACT
Lead
Mayo Clinic
PRIMARY OBJECTIVE: I. To determine changes in proliferation (Ki-67) in ER+HER2- breast cancers that receive turkey tail administration. SECONDARY OBJECTIVES: I. To assess associated adverse effects of coriolus versicolor extract (TTM). II. To determine if quality of life (QOL), mood and energy levels change while taking TTM. OUTLINE: Patients receive TTM orally (PO) twice daily (BID) starting at the time of study registration and continuing up to the day prior to standard of care (SOC) surgery (up to 20-42 days) in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up 7-30 days after last dose.
Age
18–any
Sex
FEMALE
Healthy volunteers
Not accepted
