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pirtobrutinib combined with epcoritamab

Phase 2

CLL / SLL | Small molecule | Other |Eli Lilly and Company|Trials Updated: Oct 6, 2026

Development status

Highest phase Phase 2
Registered trials 1 across 1 sponsor since Oct 2026

Success Probability

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Market & Valuation

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Trial Design

UNCONTROLLEDDMC
Total Trials1
Total Enrollment70

FDA Designations

No designations recorded

Clinical trial landscape

pirtobrutinib combined with epcoritamab · 1 trial · 1 indication

Phase 2 1
NCT07860775Treatment of Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma With Pirtobrutinib in Combination With Epcoritamab if the Disease Comes Back After Previous Treatment.CLL / SLL
NOT YET_RECRUITING70 Analytics
PHASE2NOT YET_RECRUITING
Treatment of Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma With Pirtobrutinib in Combination With Epcoritamab if the Disease Comes Back After Previous Treatment.
CLL / SLLUnlock trial analytics

Study Endpoints

Primary Endpoints

To evaluate efficacy in terms of Progression-free survival (PFS)
24 months after first dose of pirtobrutinib.

To evaluate efficacy in terms of Progression-free survival (PFS) at 24 months after first dose of pirtobrutinib.

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Study Design & Arms

AllocationNA
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Pirtobrutinib combined with epcoritamabEXPERIMENTALPirtobrutinib combined with epcoritamab

Interventions

NameTypeDescription
pirtobrutinib combined with epcoritamabCOMBINATION_PRODUCTcombination treatment
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Eligibility Criteria

Age Range18 Years to N/A
SexALL
Healthy VolunteersNo
Study Sites17

In order to be eligible to participate in this study, a patient must meet all of the following criteria: * Documented relapsed or refractory CLL or SLL (SLL in Cohort Expansion only) following at least one systemic 1st-line treatment * Requiring treatment according to International Workshop on Chro...

Countries:DenmarkNetherlandsSweden
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Recent Changes (Last 90 Days)

LOWOct 6, 2026NCT07860775NEW_TRIAL: changed
LOWOct 6, 2026NCT07860775NEW_TRIAL: changed