Nanocrystalline Megestrol Acetate for Cachectic Stage Locally Advanced Hepatocellular Carcinoma
Condition(s) studied
Investigational drug(s) / intervention(s)
Nanocrystalline Megestrol Acetate: Nanocrystalline Megestrol Acetate oral suspension, with a specification of 125 mg/mL, administered orally at a dose of 5 mL per day (625 mg/day), and the primary endpoint efficacy collection will be conducted in the 4th week.
Standard Antitumor Therapy: Standard Antitumor Therapy
Study summary
This study is a prospective, randomized, parallel-controlled clinical trial. The primary objective is to evaluate the superiority and safety of nanocrystalline megestrol acetate in combination with standard therapy compared with standard therapy alone in improving appetite and body mass index (BMI) during treatment in patients with early-stage or locally advanced hepatocellular carcinoma at the cachexia stage.
Eligibility
Primary outcome measure(s)
- The proportion of subjects with improved appetite based on A/CS-12 assessment. — The proportion of subjects with improved appetite based on A/CS-12 assessment in 12 weeks
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| West China School of Medicine/West China Hospital of Sichuan University | Chengdu | Sichuan |
More Changchun GeneScience Pharmaceutical Co., Ltd. trials in China
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07356037 on ClinicalTrials.gov ↗ ← All trials in China