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Study identifier: NCT05512390 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study to Assess the Adverse Events, Change in Disease Activity, and How Intravenously Infused ABBV-319 Moves Through the Bodies of Adult Participants With Relapsed or Refractory (R/R) Diffuse Large B-cell Lymphoma (DLBCL), Follicular Lymphoma (FL), or Chronic Lymphocytic Leukemia (CLL)

Condition: Diffuse Large B-Cell Lymphoma · Chronic Lymphocytic Leukemia · Follicular Lymphoma  ·  Sponsor: AbbVie

PhasePhase 1
Planned participants154
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

B-cell Lymphoma is an aggressive and rare cancer of a type of immune cells (a white blood cell responsible for fighting infections). Follicular Lymphoma is a slow-growing type of non-Hodgkin lymphoma. Chronic lymphocytic leukemia (CLL) is the most common leukemia (cancer of blood cells). The purpose of this study is to assess the safety, tolerability, pharmacokinetics, and preliminary efficacy of ABBV-319 in adult participants in relapsed or refractory (R/R) diffuse large b-cell lymphoma (DLBCL), R/R follicular lymphoma (FL), or R/R CLL. Adverse events will be assessed. ABBV-319 is an investigational drug being developed for the treatment of R/R DLBCL, R/R FL, or R/R CLL. This study will include a dose escalation phase to determine the doses of ABBV-319 that will be used in the next phase and a dose expansion phase to determine the change in disease activity in participants with R/R DLBCL, R/R FL, and R/R CLL. Approximately 154 adult participants with R/R B cell lymphomas including R/R DLBCL, R/R FL, and R/R CLL will be enrolled in the study in sites world wide. In the Dose Escalation phase of the study participants will receive escalating intravenously infused doses of ABBV-319 in 21-day cycles, until the Phase 2 dose is determined. In the dose expansion phase of the study participants receive intravenously infused ABBV-319 in 21-day cycles. There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend reg…

This description comes directly from the study's public registry record.

Talk to the study team

ABBVIE CALL CENTER  ·  844-663-3742  ·  abbvieclinicaltrials@abbvie.com

Always discuss trial participation with your own doctor first.

Locations (20)

University of Arizona Cancer Center - Tucson /ID# 247752Tucson, Arizona, United StatesRecruiting
Sylvester Comprehensive Cancer Center - University of Miami /ID# 247232Miami, Florida, United StatesCompleted
Allina Health System /ID# 251782Minneapolis, Minnesota, United StatesRecruiting
University of Nebraska Medical Center /ID# 246715Omaha, Nebraska, United StatesRecruiting
Memorial Sloan Kettering Cancer Center-Koch Center /ID# 249246New York, New York, United StatesRecruiting
Novant Health Presbyterian Medical Center /ID# 246719Charlotte, North Carolina, United StatesRecruiting
Baylor Sammons Cancer Center /ID# 247715Dallas, Texas, United StatesRecruiting
University of Texas Health San Antonio MD Anderson Cancer Center /ID# 256234San Antonio, Texas, United StatesRecruiting
Concord Repatriation General Hospital /ID# 249240Concord, New South Wales, AustraliaRecruiting
St Vincent's Hospital Melbourne /ID# 247624Fitzroy Melbourne, Victoria, AustraliaRecruiting
One Clinical Research Pty Ltd /ID# 248392Nedlands, Western Australia, AustraliaRecruiting
Cross Cancer Institute /ID# 246717Edmonton, Alberta, CanadaCompleted

+ 8 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05512390