Prostate Cancer Clinical Trial
Official title:
A Prospective, Randomised, Multicenter Phase II/III Clinical Trial to Evaluate the Clinical Benefit Response in Cancer Patients With Advanced Disease With AMT Versus Placebo
The purpose of the study is to evaluate the efficacy and the safety of AMT2003 in cancer
patients with advanced disease.
The primary evaluation criterion is clinical benefit response.
The study will include patients with a variety of solid tumors (i.e. esophageal, colon,
pancreatic, bronchial, gastric, hepatocellular, gall bladder, prostate and gynaecological
carcinomas.)
The clinical benefit response - CBR, is an end point that provides a clinical measure for
symptom improvement in patients. The key evaluation parameters for CBR will be assessment of
pain, the ability to perform daily activities and weight change.
;
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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