drugset / Trial / NCT07335887

Sonrotoclax Plus Dexamethasone With or Without Daratumumab Regimen in Patients With t(11;14) Primary AL Amyloidosis

NCT07335887

Phase 2 Not yet recruiting 39 enrolled Peking University People's Hospital
NaSingle-groupOpen-labelTreatment

Summary

The goal of this study is to evaluate the efficacy and safety of Sonrotoclax combined Regimen in patients with t(11;14) AL amyloidosis. Participants will receive the Sonrotoclax Plus Dexamethasone regimen with or without Daratumumab for 12 cycles. The Hematologic Response, Organ Response, Survival, and Safety will be evaluated.

Timeline

Start
2026-01-01
Primary completion
2028-02-29
Completion
2029-01-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Daratumumab Monoclonal antibody 16 mg/kg Intravenous
Subject Daratumumab Monoclonal antibody 1800 mg Intravenous
Subject Dexamethasone Small molecule 40 mg
Subject Sonrotoclax Other / unclassified

Indications