About this trial
The study is being conducted to evaluate the efficacy, and safety of Lutetium (177Lu) Oxodotreotide Injection in subjects with advanced gastrointestinal pancreatic neuroendocrine tumors.
Eligibility criteria
Qualifiers
Able and willing to provide a written informed consent;
18~75 years old,male or female;
ECOG performance status 0 or 1;
Unresectable locally advanced or metastatic gastrointestinal neuroendocrine tumors (GEP-NETs) of low and medium grade (G1 or G2) confirmed by histopathology.
Disqualifiers
Central nervous system metastasis is known. Patients who have previously received treatment ( radiotherapy or surgery ) for brain metastases and have no clinical symptoms can be enrolled if the pre-randomized pre-imaging is confirmed to be stable for at least 24 weeks;
There are clinical symptoms or diseases of the heart that are not well controlled;
Diabetes (fasting blood glucose > 2 × ULN) that cannot be well controlled after optimal medical support treatment;
Severe urinary incontinence, hydronephrosis, severe micturition dysfunction or indwelling catheter for any reason.
Trial design
Treatments tested in this trial
- Lutetium (177Lu) Oxodotreotide Injection;long-acting Octreotide
- long-acting Octreotide