Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at Los Angeles, California and other locations
Dates
study started
completion around

Description

Summary

This study is researching an experimental drug called odronextamab, referred to as study drug. The study is focused on participants with previously untreated follicular lymphoma (a type of non-Hodgkin lymphoma or NHL).

This study will be made up of two parts: Part 1 (non-randomized) and Part 2 (randomized - controlled).

The aim of Part 1 of the study is to see how safe and tolerable the study drug is when given alone.

The aim of Part 2 of the study is to see how the study drug works compared to rituximab (called the "comparator drug") and chemotherapy (the current standard of care for NHL). Standard of care means the usual medication expected and used when receiving treatment for a condition.

The study is looking at several other research questions, including:

  • What side effects may happen from taking the study drug
  • How much study drug is in the blood at different times
  • Whether the body makes antibodies against the study drug (which could make the study drug less effective or could lead to side effects)
  • How the study drug affects quality of life and ability to complete routine daily activities.

Official Title

A Phase 3, Open-label, Randomized Study to Compare the Efficacy and Safety of Odronextamab (REGN1979), an Anti-CD20 X Anti-CD3 Bispecific Antibody Versus Investigator's Choice in Previously Untreated Participants With Follicular Lymphoma (OLYMPIA-1)

Keywords

Follicular Lymphoma (FL), Non-Hodgkin lymphomas (NHLs), Indolent NHL, B-cells NHL (B-NHL), Follicular lymphoma, Odronextamab, Lymphoma, Prednisone, Prednisolone, Cyclophosphamide, Bendamustine Hydrochloride, Rituximab, Doxorubicin, Vincristine, Prednisone/prednisolone, Bendamustine

Eligibility

You can join if…

Open to people ages 18 years and up

  1. Diagnosis of Cluster of Differentiation 20^+ (CD20^+) FL Grade 1-3a, stage II bulky or stage III / IV
  2. Need for treatment as described in the protocol
  3. Have measurable disease on cross-sectional imaging documented by diagnostic imaging Computed Tomography (CT) or Magnetic Resonance Imaging (MRI)
  4. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
  5. Adequate bone marrow function and hepatic function

You CAN'T join if...

  1. Central Nervous System (CNS) lymphoma or leptomeningeal lymphoma
  2. Histological evidence of transformation to a high-grade or diffuse large B-cell lymphoma
  3. Waldenström Macroglobulinemia (WM, lymphoplasmacytic lymphoma), Grade 3b follicular lymphoma, chronic lymphocytic leukemia, or small lymphocytic lymphoma
  4. Treatment with any systemic anti-lymphoma therapy
  5. Infections and allergy/hypersensitivity to study drug or excipient

NOTE: Other protocol defined inclusion/exclusion criteria apply

Locations

  • UCLA Clinical and Translational Research Center (CTRC) accepting new patients
    Los Angeles California 90095 United States
  • University of California Irvine Medical Center (UCIMC) - Chao Family Comprehensive Cancer Center accepting new patients
    Orange California 92868 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Regeneron Pharmaceuticals
Links
Sign up for this study
ID
NCT06091254
Phase
Phase 3 Lymphoma Research Study
Study Type
Interventional
Participants
Expecting 478 study participants
Last Updated