Condition: Cancer Cachexia · Sponsor: Genfleet Therapeutics (Shanghai) Inc.
An open-label, multi-center, phase I study to evaluate the safety/tolerability and pharmacokinetics of GFS202A in advanced solid tumor patients with pre-cachexia or cachexia. The primary objective is to assess the safety/tolerability of GFS202A, determine its maximum tolerated dose (MTD), and recommend a dose range for future studies. Enroll participants with cancer cachexia or precachexia to receive GFS202A monotherapy. During the study period, participants will undergo assessments for safety and preliminary efficacy according to the visit schedule. Pharmacokinetic, anti-drug antibody (ADA), and pharmacodynamic (PD) /biomarker samples will be collected.
This description comes directly from the study's public registry record.
Yuting Peng, PM · 86+13730813620 · ytpeng@genfleet.com
Always discuss trial participation with your own doctor first.
| Sun-Yat Sen university cancer center | Guangzhou, Guangdong, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06898255