Neuroendocrine Tumors Clinical Trial
Official title:
Phase II Study of Recombinant Anti-tumor and Anti-virus Protein for Injection to Treat Advanced Neuroendocrine Tumors
The purpose of this study is to evaluate the efficacy and safety of recombinant anti-tumor and anti-virus protein for injection in treating patients with advanced neuroendocrine tumors who have failed standard treatment or are unable to receive standard treatment.
This is a Phase Ⅱ exploratory clinical study. The purpose of this study is to evaluate the
efficacy and safety of recombinant anti-tumor and anti-virus protein for injection in
treating patients with advanced neuroendocrine tumors who have failed standard treatment or
are unable to receive standard treatment.
Recombinant anti-tumor and anti-virus protein for injection, 10μg,im,3 times for the first
week, followed by 20μg for two weeks, and followed a maintenance dose of 30μg, the frequency
of administration is three times per week. Treatment continued until the patient died or had
unacceptable toxicity or had disease progression or required to discontinue the treatment.
At the time of disease progression, if investigators believe patients can continue to
benefit from the investigational product, patients may be provided with recombinant
anti-tumor and anti-virus protein for injection,but only survival follow-up datas will be
recorded.
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Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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