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A Study of LY4584180 in Adult Participants With Previously Treated Blood Cancers

RecruitingPhase 1

NOVA-BCL6-1, A First-in-Human, Multicenter Phase 1a/1b Study to Investigate Safety, Tolerability, Pharmacokinetics, and Efficacy of LY4584180 in Adult Participants With Previously Treated Hematologic Malignancies

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Has been treated for the following blood cancers and has received at least 2 prior lines of systemic therapy or not eligible for available therapy:

  * Diffuse large B-cell lymphoma - not otherwise specified
  * High-grade B-cell lymphoma
  * Diffuse large B-cell lymphoma - transformed from indolent lymphomas
  * Follicular large B-cell lymphoma
  * Follicular lymphoma
  * Other non-Hodgkin lymphoma
* Has measurable disease
* Has discontinued all previous treatments for cancer and has recovered from the immediate effects of therapy

Exclusion Criteria:

* Has an active second cancer
* Has known central nervous system (CNS) involvement by systemic lymphoma. Patients with previous treatment for CNS involvement who are neurologically stable and without evidence of active CNS disease may be eligible and enrolled if a compelling clinical rationale is provided by the Investigator and with documented Sponsor approval.
* Has known Cytomegalovirus infection. Participants with negative status are eligible
* Has known hepatitis B or C infection or uncontrolled HIV
* Has known significant heart disease

About the study

The main purpose of this study is to evaluate safety and efficacy, and measure how much LY4584180 gets into the bloodstream and how long it takes the body to eliminate it in patients with previously treated blood cancers. For each participant, the study could last about 9 months or possibly longer including screening.

What is being tested

Sponsor: Eli Lilly and Company · Participants: 460 · Started: Apr 17, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07226843

Locations in the U.S.

ArizonaMayo Clinic - Scottsdale, Scottsdale
CaliforniaCity of Hope, Duarte
University of California, Los Angeles (UCLA) - Medical Center, Los Angeles
University of California, San Francisco (UCSF) - Helen Diller Family Comprehensive Cancer Center, San Francisco
ColoradoColorado Blood Cancer Institute, Denver
FloridaUniversity of Miami - Sylvester Cancer Center, Miami
Florida Cancer Specialists - Sarasota, Sarasota
GeorgiaEmory University Hospital, Atlanta
MassachusettsDana-Farber Cancer Institute, Boston
Massachusetts General Hospital, Boston
MinnesotaMayo Clinic - Rochester, Rochester
New YorkColumbia University, New York
University of Rochester, Rochester
OhioThe Ohio State University (OSU), Columbus
OregonOregon Health & Science University (OHSU), Portland (Not yet recruiting)
TennesseeSarah Cannon Research Institute, Nashville
Vanderbilt University Medical Center, Nashville
TexasTexas Oncology - DFW (Sammons CC), Dallas
Baylor College of Medicine, Houston (Not yet recruiting)
WashingtonUniversity of Washington - Fred Hutchinson Cancer Center (Seattle Cancer Care Alliance), Seattle
WisconsinFroedtert Hospital and the Medical College of Wisconsin, Milwaukee

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.