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A Prospective, Randomized, Parallel-controlled Clinical Study of Nano-crystalline Megestrol Acetate Combined With Standard Treatment Versus Standard Treatment for First-line Extensive-stage Small Cell Lung Cancer (ES-SCLC) in the Cachexia Phase
This study is a prospective, randomized, parallel-controlled clinical trial, aiming to evaluate the efficacy and safety of nano-crystalline megestrol acetate combined with standard treatment compared to standard treatment alone as first-line therapy for extensive-stage small cell lung cancer (ES-SCLC) in both the pre-cachexia and cachexia phases. Participants enrolled in the study are those with ES-SCLC in the pre-cachexia or cachexia phase who have not received systemic treatment and are not eligible for curative therapy.
Age
18 - 85 years
Sex
ALL
Healthy Volunteers
No
West China School of Medicine/West China Hospital of Sichuan University
Chengdu, Sichuan, China
Start Date
May 1, 2025
Primary Completion Date
December 31, 2026
Completion Date
June 30, 2027
Last Updated
May 7, 2025
94
ESTIMATED participants
Nano-crystalline Megestrol Acetate Oral Suspension
DRUG
standard treatment
DRUG
Lead Sponsor
Changchun GeneScience Pharmaceutical Co., Ltd.
Collaborators
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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