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Looking for participantsPhase1

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

Sponsor: Eli Lilly and Company

NCT ID: NCT07226843

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
LY4584180 (drug), Rituximab (drug)
How long the study runs
Study runs about 46 months (dates as stated)
About the drug or intervention
LY4584180 — drug: administered orally · Rituximab — drug: administered through IV infusion
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years and over
Who
All
Number of participants
460
Started
2026-04-17
Last checked
2026-10

Plain English Summary

What is this study?

  • • Testing a new treatment for lymphoma, non-hodgkin's
  • • Phase1 - 460 participants
  • • 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

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with lymphoma, non-hodgkin's

Where?

  • • London - King's College Hospital
  • • London - The Royal Marsden NHS Foundation Trust
  • • Nottingham - Nottingham City Hospital
  • • Plymouth - Derriford Hospital
  • • +1 more UK sites

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

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.

Lymphoma, Non-Hodgkin'sLymphoma, Diffuse Large B-CellFollicular Lymphoma

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

Biomarkers mentioned

with negative

What the study is looking for

  • ✓Has been treated for the following blood cancers and has received at least 2 previous treatments or not...
  • ✓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

Who cannot take part

  • ✗Has an active second cancer
  • ✗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
See the full 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

Where Is This Study? (5 UK sites)

King's College Hospital

London SE5 9RS, United Kingdom

NOT_YET_RECRUITING
Hospital R&D contact (matched)

Jasmine Palmer

kch-tr.research@nhs.net0203 299 1980

The Royal Marsden NHS Foundation Trust

London SW3 6JJ, United Kingdom

NOT_YET_RECRUITING
Hospital R&D contact (matched)

Mark Brandon-Grove

research.development@rmh.nhs.uk020 3186 5416

Nottingham City Hospital

Nottingham NG5 1PB, United Kingdom

NOT_YET_RECRUITING
Hospital R&D contact (matched)

Alison Lloyd

nuhnt.researchsponsor@nhs.net0115 9249924

Derriford Hospital

Plymouth PL6 8DH, United Kingdom

NOT_YET_RECRUITING

University Hospital Southampton NHS Foundation Trust

Southampton SO16 6YD, United Kingdom

NOT_YET_RECRUITING
Hospital R&D contact (matched)

Dr Mikayala King

researchmanagement@uhs.nhs.uk023 81208215

How to Get in Touch

Trial question or participation questions: 1-877-CTLILLY (1-877-285-4559) or

Sponsor contact

CONTACT

1-317-615-4559 LillyTrials@Lilly.com

Physicians interested in becoming principal investigators please contact

Sponsor contact

CONTACT

clinical_inquiry_hub@lilly.com
Data sourced from ClinicalTrials.gov · Last verified: 2026-10