A Study of JMT203 in Patients With Cancer Cachexia

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorShanghai JMT-Bio Inc.

About this trial

A Phase Ia/II, Multicenter Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of JMT203 in Patients with Cancer Cachexia

Eligibility criteria

Qualifiers

Age ≥ 18 years old;

Voluntarily participate in the study and sign the informed consent form;

Age ≥ 18 years old;

Voluntarily participate in the study and sign the informed consent form;

Disqualifiers

Presence of reversible causes leading to decreased food intake;

Patients with dysphagia or poor food digestion and absorption, including gastrointestinal obstruction, active inflammatory bowel disease, or short bowel syndrome;

Patients with cachexia caused by clearly identified other causes, such as severe chronic obstructive pulmonary disease, uncontrolled thyroid disease, vital organ failure, or Acquired Immune Deficiency Syndrome (AIDS);

Patients receiving tube feeding or parenteral nutrition therapy during the screening period;

Trial design

Treatments tested in this trial

  • JMT203 Injection
  • JMT203 Injection

Treatment groups

307 Participants
are divided into 4 treatment groups

Sponsors and collaborators