OncoMatch/Clinical Trials/NCT06868849
A Study of JMT203 in Patients With Cancer Cachexia
Is NCT06868849 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies JMT203 for colorectal cancer.
Treatment: JMT203 — This is an open-label, multicenter Phase I clinical study aimed at evaluating the safety/tolerability, pharmacokinetics, and effectiveness of JMT203 in patients with cancer cachexia.
Check if I qualifyExtracted eligibility criteria
Cancer type
Colorectal Cancer
Small Cell Lung Cancer
Pancreatic Cancer
Biomarker criteria
Required: GDF15 serum GDF-15 ≥1300 pg/ml (≥1300 pg/ml)
Serum Growth Differentiation Factor 15 (GDF-15) levels ≥1300 pg/ml within 28 days prior to the first study drug administration (applicable to the cohort expansion phase only)
Performance status
ECOG 0–2(Ambulatory, capable of self-care)
Prior therapy
Must have received: anti-tumor treatment — ongoing or completed
ongoing or completed anti-tumor treatment, and no significant tumor progression within 28 days prior to the first drug administration
Cannot have received: prescription medications for appetite enhancement or improve weight loss (anamorelin, medroxyprogesterone acetate, dronabinol, medical marijuana)
Patients who have taken any prescription medications for appetite enhancement or improve weight loss within 28 days or 5 half-lives (whichever is shorter) before the first study drug administration
Cannot have received: systemic glucocorticoids (prednisone)
Exception: excluding pretreatment for antitumor therapy
Initiation of systemic glucocorticoids (prednisone >10 mg/day or equivalent doses of other similar drugs) or other immunosuppressive therapies within 28 days before the first study drug administration, excluding pretreatment for antitumor therapy
Cannot have received: tube feeding or parenteral nutrition therapy
Patients receiving tube feeding or parenteral nutrition therapy during the screening period
Cannot have received: other clinical study medications
Patients who have received other clinical study medications within 4 weeks or 5 half-lives (whichever is shorter) before the first study drug administration
Lab requirements
Blood counts
Absolute Neutrophil Count ≥1.0×10^9/L; Platelet Count ≥75×10^9/L; Hemoglobin ≥80 g/L
Kidney function
Serum Creatinine ≤1.5×ULN (if >1.5×ULN, creatinine clearance calculated by the Cockcroft formula must≥30 ml/min)
Liver function
Total Bilirubin ≤1.5×ULN (For patients with liver metastasis, liver cancer, or bile duct obstruction: may be relaxed to ≤3×ULN); AST and ALT ≤3×ULN or ≤5×ULN for patients with liver metastasis
Adequate organ function, meeting relevant laboratory test standards
Structured fields extracted by AI. May contain errors — verify against the official protocol.
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