drugset / Trial / NCT07130617

Evaluation of the Efficacy and Safety of Megestrol Acetate in Preventing Nausea and Vomiting Induced by Highly Emetogenic Chemotherapy

NCT07130617

Phase 1 Not yet recruiting 132 enrolled Changchun GeneScience Pharmaceutical Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To evaluate the efficacy of Megestrol Acetate Oral Suspension in Preventing Nausea and Vomiting Induced by Highly Emetogenic Chemotherapy in Malignant Solid Tumor Patients

Timeline

Start
2025-09-29
Primary completion
2026-07-31
Completion
2026-07-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Megestrol Acetate Other / unclassified 312.5 mg Oral
Subject Megestrol Acetate Other / unclassified 625 mg Oral
Subject Megestrol Acetate Other / unclassified 937.5 mg Oral

Indications

No indication recorded.