To evaluate the safety of DCC-2618 in patients with unresectable, metastatic, or recurrent gastrointestinal stromal tumor (GIST) who have received three or more prior therapies
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
DCC-2618 150 mg, administered orally once daily
National Cancer Center Hospital East
Kashiwa, Chiba, Japan
National Cancer Center Hospital
Tokyo, Chuo-ku, Japan
Adverse event (AE)
Time frame: Up to 2 years
North America Clinical Trial Support Desk
CONTACT
International Clinical Trial Support Desk
CONTACT
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.