drugset / Trial / NCT04612582

Comparison of BTD and BCD Based Regimens in the Treatment of AL Amyloidosis

NCT04612582

Phase 4 Unknown 70 enrolled Guangdong Provincial People's Hospital
RandomizedParallel-groupOpen-labelTreatment

Summary

Research Objective:At present, there is no standard therapeutic regimen for monoclonal immunoglobulin light chain (AL) amyloidosis in the world. To compare the efficacy and safety of the regimens between bortezomib-thalidomide-dexamethasone (BTD) and bortezomib-cyclophosphamide-dexamethasone (BCD) in the treatment of AL amyloidosis, so as to provide more clinical evidence for the standard treatment for the disease. Research Design:This study was designed as a prospective, randomized and controlled clinical study. Patients who meet the inclusion criteria of this study will be randomized to the BTD scheme group or BCD scheme group.

Timeline

Start
2020-01-01
Primary completion
2023-01-31
Completion
2023-06-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclophosphamide Other / unclassified 900 mg/m2 Intravenous
Subject Thalidomide Other / unclassified 50 mg Oral
Subject Thalidomide Other / unclassified 100 mg Oral
Background Bortezomib Small molecule 1.3 mg/m2 Subcutaneous
Background Dexamethasone Small molecule 20 mg Oral

Indications