drugset / Trial / NCT04780464

A 3 Arm Randomized Study on Health-related QoL of Elderly Patients With Advanced Soft Tissue Sarcoma

NCT04780464

RandomizedParallel-groupOpen-labelTreatment

Summary

This is a multi-centre, open label, randomized phase 3 selection study (1:2:2 randomization). After confirmation of the eligibility criteria, 185 patients will be randomized 1:2:2 to either the control arm (doxorubicin 60-75 mg/m² IV every 3 weeks) or experimental arm 1 (doxorubicin 12 mg/m2 IV every week) or experimental arm 2 (cyclophosphamide 100 mg orally BD plus prednisolone 10-20 mg orally on day 1 to day 7 of each 14 day cycle). HRQoL assessment will be performed every 3 weeks during the first 12 weeks and every 12 weeks thereafter until month 12 after start of treatment. Disease evaluation will be performed every 12 weeks until progression. The primary endpoint of the study is difference among the study arms in physical and role functioning at 12 weeks.

Timeline

Start
2022-04-11
Primary completion
2023-09-22
Completion
2023-11-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclophosphamide Other / unclassified 100 mg Oral
Subject Doxorubicin Other / unclassified 12 mg/m2 Intravenous
Subject Doxorubicin Other / unclassified 60 mg/m2 Intravenous
Subject Doxorubicin Other / unclassified 75 mg/m2 Intravenous
Subject Prednisolone Other / unclassified 10 mg Oral
Subject Prednisolone Other / unclassified 20 mg Oral
Subject Prednisone Other / unclassified 10 mg
Subject Prednisone Other / unclassified 20 mg

Indications