Clinical Trial

An Phase I/IIa Clinical Study to Evaluate the Safety/Tolerability, Pharmacokinetics and Preliminary Efficacy of INB301 Injection in Patients With Cancer Cachexia

Not Yet Recruiting Phase 1/2
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Summary
This is an open-label, multicenter, multiple-dose Phase I/IIa clinical study to assess the safety/tolerability, PK characteristics,immunogenicity, and preliminary efficacy of INB301 Injection in patients with cancer cachexia. The indication to be explored for Phase I is malignant solid tumor with cachexia; Phase IIa will determine the specific study cohort after discussion between the investigator and the sponsor based on the previously obtained clinical trial data and the benefit/risk ratio of the subjects, and preliminarily consider 3 cohorts of tentative 20-30 patients each, including non-small cell lung cancer, pancreatic cancer and colorectal cancer with cachexia.
Trial Details
NCT Number NCT07584057
Lead Sponsor Yunnan Baiyao Group Co., Ltd.
Conditions Cancer Cachexia
Enrollment 146 participants
Start Date 2026-05
Primary Completion 2030-02 (estimated)
Study Completion 2030-03 (estimated)
Updated on ClinicalTrials.gov 2026-05-13