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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.

Phase 1RecruitingShanghai JMT-Bio Inc.NCT06868849Data as of May 2026

Treatment: JMT203This 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.

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Extracted 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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