Finding studies
Finding studies
Take this into the appointment.
Saves the questions and what to expect into your notes, next to the visit they belong to.
Liron Dimnik
CONTACT
Aviya Hoida
CONTACT
Lead
Alpha Tau Medical LTD.
This study will be a prospective, interventional, open label, single arm, multiple center study. Patients who have been previously treated with 8 - 12 cycles of mFOLFIRINOX will undergo DaRT insertion, with the goal of making their tumor resectable. Three (3) days after DaRT insertion, patients will begin taking Capecitabine for 2 months. Every 2 months after DaRT insertion, the patient will be assessed to determine if their tumor is surgically resectable, if they should continue with therapy, or if they should pause therapy. The trial will end 12 months after DaRT insertion.
Age
18–120
Sex
ALL
Healthy volunteers
Not accepted
