RecruitingPhase 2NCT07162181

Long-Term Safety of Pirtobrutinib in Participants With Previously Treated Types of Blood Cancers

Long-Term Safety of Pirtobrutinib in Participants From Study J2N-MC-JZNJ With Previously Treated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma or Non-Hodgkin Lymphoma


Sponsor

Eli Lilly and Company

Enrollment

13 participants

Start Date

Aug 7, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to find out more about the long-term safety of pirtobrutinib in participants with previously treated types of blood cancer. Participants must have chronic lymphocytic leukemia, small lymphocytic lymphoma, or non-Hodgkins lymphoma. The study is open to those who completed the original study - J2N-MC-JZNJ (NCT04849416) and continue to benefit from treatment. Treatment will be given every 12 weeks and this study is expected to last about 5 years.


Eligibility

Min Age: 18 Years

Inclusion Criteria2

  • Currently enrolled and active in the originator study, JZNJ. A participant is considered active in the study if they are receiving study intervention
  • Agree to comply with contraception requirements. Contraceptive use by participants should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies

Exclusion Criteria1

  • Are pregnant, or intend to become pregnant during the study, or within 30 days of last dose of study treatment or to breastfeed during the study or within 1 week of the last dose of study treatment

Interventions

DRUGPirtobrutinib

Administered orally.


Locations(6)

Beijing Cancer hospital

Beijing, China

Sun Yat-sen University Cancer Center

Guangzhou, China

Harbin Medical University Cancer Hospital

Harbin, China

Shanghai East Hospital

Shanghai, China

Blood Institute of the Chinese Academy of Medical science

Tianjin, China

Union Hospital Tongji Medical College Huazhong University of Science and Technology

Wuhan, China

View Full Details on ClinicalTrials.gov

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NCT07162181


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