About this trial

This is a single-center, phase 2, open-label clinical trial of a novel combination of polatuzumab vedotin, glofitamab, and tafasitamab (TPG) as first-line treatment of patients with diffuse large B cell lymphoma (DLBCL) or high-grade B cell lymphoma (HGBL).

Eligibility criteria

Qualifiers

Ability to understand and the willingness to sign a written informed consent document and to comply with the study protocol procedures.

Age ≥18 years.

Diffuse large B-cell lymphoma, not otherwise specified (NOS)

T-cell/histiocyte-rich large B-cell lymphoma

Disqualifiers

Pregnancy, breast-feeding, or prisoner status.

Central nervous system involvement by the lymphoma.

Prior solid organ transplantation or allogeneic stem cell transplantation.

History of severe allergic or anaphylactic reactions to humanized or murine monoclonal antibodies or known sensitivity or allergy to murine products.

Trial design

Treatments tested in this trial

  • Tafasitamab
  • Polatuzumab vedotin
  • Glofitamab
  • Obinutuzumab

Treatment groups

30 Participants
are divided into 1 treatment group

Locations

1
Rhode Island Hospital02903, ProvidenceRhode Island, United States

Sponsors and collaborators

Brown University

Lead sponsor

Incyte Corporation

Collaborator

Genentech, Inc.

Collaborator

Natera, Inc.

Collaborator