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Clinical Trial Summary

This is a prospective and single arm clinical study. The goal of this clinical trial is to observe and evaluate the efficacy and safety of Daratumumab/daratumumab and hyaluronidase-fihj in combination with pomalidomide and dexamethasone in the treatment of patients with newly diagnosed AL amyloidosis.


Clinical Trial Description

Primary objective: Hematologic overall remission rate (ORR) as defined by the criteria in the Chinese Guidelines for the Diagnosis and Treatment of Systemic Light Chain Amyloidosis, 2021 edition. Secondary objective: 1. organ remission rate as defined by the criteria of the Chinese Guidelines for the Diagnosis and Treatment of Systemic Light-Chain Amyloidosis 2021 Edition, hematologic complete remission (CR) rate, very good partial remission (VGPR) rate, progression free survival (PFS), overall survival (OS), and negative rate of microscopic residual disease (MRD). 2. safety of combination therapy regimens. Exploratory purpose: EORTC QLQ-C30. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06455748
Study type Interventional
Source First Affiliated Hospital of Wenzhou Medical University
Contact Yongyong Ma, MD
Phone +86-13566281793
Email mayy@wmu.edu.cn
Status Recruiting
Phase N/A
Start date March 1, 2024
Completion date March 1, 2025