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Looking for participantsPhase4

A Study of Pirtobrutinib (LY3527727) in Participants With Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

Sponsor: Eli Lilly and Company

NCT ID: NCT07218341

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
Pirtobrutinib (drug), Idelalisib (drug)
How long the study runs
Study runs about 81 months (dates as stated)
About the drug or intervention
Pirtobrutinib — drug: Administered orally · Idelalisib — drug: Administered orally
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years and over
Who
All
Number of participants
150
Started
2026-03-09
Last checked
2026-09

Plain English Summary

What is this study?

  • • Testing a new treatment for chronic lymphocytic leukemia
  • • Phase4 - 150 participants
  • • This study will evaluate the long-term safety of pirtobrutinib in participants with previously treated chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL)

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with chronic lymphocytic leukemia

Where?

  • • Hull - Castle Hill Hospital
  • • Leeds - St James's University Hospital
  • • Newmarket - GenesisCare

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

About This Trial

This study will evaluate the long-term safety of pirtobrutinib in participants with previously treated chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL). The study is open to those who completed J2N-MC-JZNN/LOXO-BTK-20020 (NCT 04666038) for continued access to the study intervention or continued follow-up visits. Treatment will be given every 4 weeks and this study is expected to last about 5 years.

Chronic Lymphocytic LeukemiaLymphoma, Small Lymphocytic

How this trial compares with your answers

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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

What the study is looking for

  • ✓Are actively participating in study J2N-MC-JZNN/LOXO-BTK-20020

Who cannot take part

  • ✗This is not applicable to this study
See the full criteria
Inclusion Criteria: * Are actively participating in study J2N-MC-JZNN/LOXO-BTK-20020 Exclusion Criteria: * This is not applicable to this study

Where Is This Study? (3 UK sites)

Castle Hill Hospital

Hull HU16 5JQ, United Kingdom

NOT_YET_RECRUITING
Site contact (verified)
David AllsupPrincipal Investigator

St James's University Hospital

Leeds LS9 7TF, United Kingdom

Recruiting
Site contact (verified)
Talha MunirPrincipal Investigator

GenesisCare

Newmarket CB8 7XN, United Kingdom

NOT_YET_RECRUITING
Site contact (verified)
George FollowsPrincipal Investigator

How to Get in Touch

Trial questions 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: 2026-09