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A Prospective Real-World Observational Study of Nanocrystalline Megestrol Acetate in Patients With Cancer Cachexia
Sponsor: Changchun GeneScience Pharmaceutical Co., Ltd.
Summary
This study is a prospective, real-world observational study. The objective is to evaluate the effectiveness and safety of nanocrystalline megestrol acetate in patients with cancer cachexia in real-world settings. Eligible participants were patients diagnosed with cancer cachexia who were scheduled to receive treatment with nanocrystalline megestrol acetate.
Key Details
Gender
All
Age Range
18 Years - 85 Years
Study Type
INTERVENTIONAL
Enrollment
495
Start Date
2025-09-25
Completion Date
2027-06-30
Last Updated
2025-11-21
Healthy Volunteers
No
Conditions
Interventions
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.
Locations (1)
Henan Cancer Hospital, Affiliated to Zhengzhou University
Zhengzhou, Henan, China