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Anamorelin study for gastrectomized patients with unresectable advanced or recurrent gastric cancer

Specified Clinical Trial for the Evaluation of Anamorelin Hydrochloride in Gastrectomized Patients Under Post-surgical Chemotherapy of Recurrent Gastric Cancer or Unresectable Advanced Gastric Cancer - TEAM-GUSTO study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs051210108
Enrollment
200
Registered
2021-10-13
Start date
2021-11-17
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Unresectable advanced or recurrent gastric cancer and cachexia Cancer cachexia, Gastric cancer, Gastrectomy

Interventions

Administration of anamorelin for unresectable advanced or recurrent gastric cancer

Sponsors

Doki Yuichiro
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Recurrent gastric cancer over 3 months after gastrectomy or unrectable advanced gastric cancer (2) Planning a new line of 1st-3rd chemotherapy or receiving 1st-3rd chemotherapy (3) Involuntary weight loss of >=5% observed within the previous 6 months (4) Fulfilling at least 2 items of following criteria 1. Fatigue 2. Decreased general muscle strength 3. Fulfilling at least one item of following criteria i. CRP>0.5mg/dL ii. Hb=20 years at the time of informed consent (6) Life expectancy >= 4 months from the time of informed consent (7) Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 (8) Adequate organ (Bone marrow, hepatic, renal) function 1. WBC: >=2,500/mm3, =10x104/mm3 3. Hb: >=8g/dL 4. AST (GOT): <=150U/L 5. ALT (GPT): <=180U/L 6. Cre: <=2.0mg/dL (9) with written informed consent

Exclusion criteria

Exclusion criteria: (1) Previous history of administration of anamorelin (2) Previous history of allergy for ingredients of anamorelin (3) Previous history of congestive heart failure (4) Myocarical infarction or cardica angina (5) Severe dysfunction of impulse conducting system (complete AV block etc.) (6) Taking prescription medications with: Clarithromycin, Indinavir, Itraconazole, Nelfinavir, Saquinavir, Telaprevir, Voriconazole, Ritonavir, Cobicistat (7) Moderate liver dysfunction (Child-Pugh classification B or C) (8) Inability of taking orally due to bowel abnormality (e.g., bowel obstruction) (9) Poor control of diabetes mellitus (10) Pregnant or possibility of pregnancy (11) Active synchronous or metachronous malignancies (excluding carcinoma in situ) (12) Self-contained mechanical device such as pacemaker (13) Judged by doctors as inadequate

Design outcomes

Primary

MeasureTime frame
Changes of lean body mass

Secondary

MeasureTime frame
1. Transition of lean body mass 2. Change in body weight 3. Transition of body weight 4. Body composition (Fat mass) 5. Transition of body composition (Fat mass) 6. Skeletal muscle index (SMI) 7. Transition of Cancer fatigue scale 8. Grip strength 9. Transition of grip strength 10. Relative Dose Intensity of chemotherapy 11. Change of QOL-ACD score 12. Transition of QOL-ACD score 13. Blood examinations for assessment of nutritional states 14. CTCAE grade of 3 items related with chemotherapy-induced adverse events: anorexia, nausea, vomiting 15. Chemotherapy response judged by RECIST ver1.1

Contacts

Public ContactKazuyoshi Yamamoto

The University of Osaka Hospital

kyamamoto13@gesurg.med.osaka-u.ac.jp+81-6-6879-5111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026