• Home
  • Study Details
Open

Zilovertamab Vedotin+R-CHP vs Polatuzumab Vedotin+R-CHP for 1L DLBCL, GCB

The purpose of this study is to evaluate the efficacy and safety of zilovertamab vedotin plus R-CHP versus polatuzumab vedotin plus R-CHP for the treatment of the GCB subtype of DLBCL.

Age & Gender

  • 18 years ~ 99 years
  • Male, Female, Gender Inclusive

Visit Availability

  • Standard business hours (M-F, 8-5)
  • Visits can be combined with regular clinical appointments

Location

International (Germany, Ireland, Italy, United Kingdom)

What will be asked of you

Use a handheld device (tablet) at the trial site to answer questionnaires about your symptoms and your ability to do common activities in your daily life. Have a physical exam. Give blood and urine (pee) samples. If you are getting zilovertamab vedotin (Group 1), you will give multiple blood samples at some visits. For example, you may need to give a blood sample before and after getting zilovertamab vedotin, and then 4 hours after trial treatment. You will also have to return to the trial site 2 times in the 2 weeks after your first infusion of zilovertamab vedotin to have your blood drawn. Have an echocardiogram (ECHO) or multiple-gated acquisition (MUGA) Have an electrocardiogram (ECG). Have scans using computed tomography (CT), magnetic resonance imaging (MRI), positron emission tomography (PET), or other tests. Have a bone marrow biopsy at the beginning of the trial. Have a tumor biopsy or give tumor tissue from an earlier biopsy at the beginning of the trial.

Incentives

$50 per completed visit

Total length of participation:
65 months

Looking for Specific Volunteers

Able to participate:

  • You have been diagnosed with GCB subtype of diffuse large B-cell lymphoma (DLBCL)
  • You have not not received prior treatment for DLBCL

Not eligible if:

  • You have a history of transformation of indolent disease to DLBCL
  • You have received a diagnosis of PMBCL or Grey zone lymphoma
  • You have Ann Arbor Stage I DLBCL.
  • You have active CNS lymphoma
  • You have clinically significant cardiac (heart) disease

Contact the Team

Visit Location

Contact & Visit Location

Primary Contact

Primary Visit Location

Lineberger Comprehensive Cancer Center
NC Cancer Hospital (Basnight)
UNC Hospitals / UNC Medical Center
101 Manning Dr, Chapel Hill, NC 27514, USA

Additional Study Information

Principal Investigator

Natalie Grover
LCCC - Clinical Trials

Study Type

Clinical or Medical
Interventional

Study Topics

Cancer (Lymphoma)

IRB Number

25-0288

Research for Me logo

Copyright © 2013-2022 The NC TraCS Institute, the integrated home of the NIH Clinical and Translational Science Awards (CTSA) Program at UNC-CH.  This website is made possible by CTSA Grant UL1TR002489 and the National Center for Advancing Translational Sciences.

Questions?

  • This email address is being protected from spambots. You need JavaScript enabled to view it.
logo for the North Carolina Translational and Clinical Sciences Institute
logo for UNC Health
logo for UNC School of Medicine
logo for UNC Research