A Study of (LY3527727) Pirtobrutinib in Participants With Previously Treated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma or Non-Hodgkin Lymphoma
Recruiting
Phase 4Interventional Study
Chronic Lymphocytic LeukemiaNon-Hodgkin Lymphoma
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
279 (estimated)
Sponsor
Eli Lilly and Company · Industry
Who this trial is looking for
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Study J2N-MC-JZ01 (JZ01) is an individual-study appendix (ISA) under master protocol J2N-MC-JZNY, and represents participants from the completed originator study, clinical study LOXO-BTK-18001/J2N-OX-JZNA. Participants in the originator study will have the opportunity to continue their assigned study intervention or continue their follow-up visits by transitioning to this study. This study will ev…
Study J2N-MC-JZ01 (JZ01) is an individual-study appendix (ISA) under master protocol J2N-MC-JZNY, and represents participants from the completed originator study, clinical study LOXO-BTK-18001/J2N-OX-JZNA. Participants in the originator study will have the opportunity to continue their assigned study intervention or continue their follow-up visits by transitioning to this study. This study will evaluate the long-term safety and efficacy of pirtobrutinib.
Trial Locations
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Status
Eligibility Criteria
Inclusion Criteria:
* Are currently enrolled and active in the originator study, LOXO-BTK-18001. A participant is considered active in the study if they are:
* receiving study intervention
* in the short-term follow-up period, or
* in the long-term follow-up period
Exclusion Criteria:
* We…
Inclusion Criteria:
* Are currently enrolled and active in the originator study, LOXO-BTK-18001. A participant is considered active in the study if they are:
* receiving study intervention
* in the short-term follow-up period, or
* in the long-term follow-up period
Exclusion Criteria:
* Were a participant in the Phase 1b cohort of Study LOXO-BTK-18001
Contacts
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or
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