gastric cancer/ colorectal cancer/ pancreatic cancer
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: a. Patients who are eligible for administration of anamorelin b. Patients who have obtained the written consent of the patient or his/her substitute to participate in the study
Exclusion criteria
Exclusion criteria: a. Patients with contraindications to the administration of anamorelin b. Patients who are judged by the attending physician, or the department or facility to which the attending physician belongs, to be undesirable to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improvement in physical functions after 12 weeks of anamorelin administration | — |
Secondary
| Measure | Time frame |
|---|---|
| change from baseline in dietary intake, ECOG performance status(PS),lean body mass(LBM),total weight,physical functions, physical function's satisfaction,adverse events,overall survival(OS),duration of treatment, progression-free survival(PFS),objective response rateand(ORR),disease control rate(DCR),efficacy,safety,predictive factors for treatment efficacy and safety in patirnts with gastric/colorectal/pancreatic cancer by early induction of multimodel care with anamorelin administration,nutritional and excercise at each assessment period. | — |
Countries
Japan
Contacts
Hitachi General Hospital Department of pharmacy