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Clinical Trial Summary

This is an open-label, multicenter, Phase 2 study in subjects with newly diagnosed monoclonal immunoglobulin deposition disease treated with daratumumab, bortezomib, cyclophosphamide, and dexamethasone.


Clinical Trial Description

The current study aims to investigate daratumumab, bortezomib, cyclophosphamide, and dexamethasone regimen in patients with newly diagnosed monoclonal immunoglobulin deposition disease. Approximately 25 subjects will receive primary therapy with daratumumab-CyBorD. The primary endpoint is overall complete hematologic response (CHR) rate at 6 months. ;


Study Design


Related Conditions & MeSH terms

  • Immunoglobulin Light-chain Amyloidosis
  • Monoclonal Gammopathy of Renal Significance
  • Monoclonal Gammopathy of Undetermined Significance
  • Paraproteinemias

NCT number NCT06418477
Study type Interventional
Source Peking University People's Hospital
Contact Jin Lu
Phone 86-13311491805
Email jin1lu@sina.com
Status Recruiting
Phase Phase 2
Start date May 28, 2024
Completion date December 31, 2026

See also
  Status Clinical Trial Phase
Recruiting NCT06083922 - A Study of CyBorD (Cyclophosphamide, Bortezomib, Dexamethasone) Plus Daratumumab in People With Monoclonal Gammopathy of Renal Significance (MGRS) Phase 2
Completed NCT05119309 - MGRS: Clinical-histological Features of a Multicenter Case Series
Recruiting NCT03629561 - Diagnosis of MGRS in Patients With Paraproteinemias: Clinical, Anatomopathological and Pathophysiological Study