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NCT06898255

A Phase I Study to Evaluate GFS202A in Advanced Solid Tumor Patients With Pre-cachexia or Cachexia

Recruiting now Phase 1 Last updated 5 June 2025
What this trial tests

Phase 1 trial testing GFS202A injection in Cancer Cachexia in 36 participants. Currently enrolling.

Timeline
24 April 2025
Primary endpoint
8 June 2026
6 July 2026

Quick facts

Lead sponsorGenfleet Therapeutics (Shanghai) Inc.
PhasePhase 1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationnon randomized
Designsequential
Maskingnone
Primary purposetreatment
Enrollment36
Start date24 April 2025
Primary completion8 June 2026
Estimated completion6 July 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Genfleet Therapeutics (Shanghai) Inc. — full company profile →

Who can join

Adults 18 to 80, any sex, with Cancer Cachexia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Cancer Cachexia

Currently open trials in the same condition.

Other Genfleet Therapeutics (Shanghai) Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06898255.

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