Cachexia Clinical Trial
Official title:
Double-Blind, Placebo-Controlled, Dose-Finding Study of the Effect of GTx-024 on Muscle Wasting (Cachexia) in Patients With Cancer
The purpose of this study is to assess if Gtx-024 is effective in increasing lean body mass in subjects with muscle wasting related to cancer.
Cancer cachexia is characterized by a hypermetabolic state that leads to catabolism that is
responsible for reductions in lean mass.These catabolic changes are accompanied by an
increase in total energy expenditure, but a decrease in voluntary energy expenditure that
ultimately results clinically in cachexia and its symptoms of lethargy, fatigue, weakness
and general malaise (Kotler DP. Cachexia. Ann Intern Med. 2000; 133:622-634).
The prevalence of cachexia increases from 50 percent at presentation to more than 80 percent
before death from malignancy. In over 20 percent of cancer patients, cachexia is the cause
of death (Bruera E. Anorexia, cachexia and nutrition. Br Med J 1997;315:1219-1222). Cancer
cachexia leads to shorter survival, decreased response rates and increased toxicity to
chemotherapy, weakness, and an overall decreased quality of life (DeWys et al. Prognostic
effect of weight loss prior to chemotherapy in cancer patients. Eastern Cooperative Oncology
Group. Am J Med. 1980 Oct;69(4):491-7). The purpose of this study is to assess the efficacy
of GTx-024 on total body lean mass. Secondary endpoints include but are not limited to
assessment of GTx-024 on muscle function, total body weight and total body fat mass.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Supportive Care
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