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

Part of paid clinical trials in Scottsdale, Arizona.

Sponsor
Eli Lilly and Company
Study ID
NCT07226843
Phase
PHASE1
Status
Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

Study Details

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.

Key Dates

Start date
Apr 17, 2026
Status verified
Jun 2026
Primary completion
Apr 30, 2027
Completion
Feb 28, 2030

Study Design

Enrollment
460 participants (estimated)
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Phase 1a-Monotherapy Dose Escalation (Cohort A1)
    LY4584180 monotherapy administered orally
  • Experimental: Phase 1a-Monotherapy Dose Optimization (Cohort A2)
    LY4584180 monotherapy administered orally
  • Experimental: Phase 1b-Dose Expansion-Monotherapy (Cohort B1-B3)
    LY4584180 monotherapy administered orally
  • Experimental: Phase 1b-Dose Expansion-Combination (Cohort B4)
    LY4584180 administered orally in combination with rituximab administered through IV infusion

Primary Outcome Measure

Number of Dose-Limiting Toxicities (DLTs) and DLT-Equivalent Toxicities [ Time Frame: Baseline up to Day 28 ]

Central Contacts

  • Trial question or participation questions: 1-877-CTLILLY (1-877-285-4559) or
    1-317-615-4559
  • Physicians interested in becoming principal investigators please contact

Locations (21)

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