Pilot Study of Daratumumab in Combination With Bortezomib, Cyclophosphamide, and Dexamethasone (Dara-CyBorD) in Newly Diagnosed Multiple Myeloma Patients With Renal Failure

Status: Recruiting
Location: See location...
Intervention Type: Combination product
Study Type: Interventional
Study Phase: Early Phase 1
SUMMARY

The goal of this study is to assess the efficacy of induction treatment with daratumumab-hyaluronidase (dara SC) with cyclophosphamide, bortezomib, and dexamethasone (Dara-CyBorD) for four cycles in patients with newly diagnosed multiple myeloma who have new onset renal failure. This study will also investigate the difference responses in African American (AA) patients versus non-African American patients. The primary questions this study aims to answer are: 1. To evaluate the very good partial response rate (VGPR) after 4 cycles of Dara-CyBord. 2. To evaluate the renal response rate (RRR) after 4 cycles of Dara-CyBord.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Patients must have had a confirmed new diagnosis of MM following revised IMWG criteria.

• Patients must have Zubrod/ECOG Performance Status ≤ 2.

• Patients must have renal insufficiency. Renal insufficiency is defined as eCrCl \< 60 mL/min (using Cockcroft-Gault Equation for Cr Cl) and/or necessitating dialysis

• must not have known allergies to any of the study drugs. Must have adequate organ function.

• International normalized ratio (INR) and prothrombin time (PT) ≤1.5 × ULN. Activated partial thromboplastin time (aPTT) ≤1.5 × ULN.

Locations
United States
Georgia
Georgia Cancer Center-Augusta University
RECRUITING
Augusta
Contact Information
Primary
Amany RA Keruakous, MD
AKERUAKOUS@augusta.edu
706-721-2505
Backup
James T Sonnenberg, BS
jsonnenberg@augusta.edu
9106192597
Time Frame
Start Date: 2024-11-01
Estimated Completion Date: 2027-11-01
Participants
Target number of participants: 30
Treatments
Experimental: Dara-CyBorD
Induction treatment with daratumumab-hyaluronidase (dara SC) in combination with cyclophosphamide, bortezomib, and dexamethasone (Dara-CyBorD) for four cycles of 28 days, followed by restaging with repeat PET-CT, bone marrow evaluation, and myeloma serological testing.
Related Therapeutic Areas
Sponsors
Leads: Augusta University
Collaborators: Janssen Scientific Affairs, LLC

This content was sourced from clinicaltrials.gov

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