Study on Pirtobrutinib for Patients with Previously Treated Chronic Lymphocytic Leukemia or Non-Hodgkin Lymphoma

Sponsor: Eli Lilly and Company

Sponsor score: 60

ClinicalTrials ID:NCT06876662

This study is for patients who have already participated in a previous trial and are continuing their treatment or follow-up. It aims to assess the long-term safety and effectiveness of the drug Pirtobrutinib for those with Chronic Lymphocytic Leukemia or Non-Hodgkin Lymphoma.

Patient Parameters

Program Overview

This study is a continuation for participants from a previous trial who are either still receiving treatment or are in follow-up stages. It focuses on evaluating how safe and effective Pirtobrutinib is over a longer period for patients with Chronic Lymphocytic Leukemia or Non-Hodgkin Lymphoma.

Eligibility Criteria

Inclusion Criteria

  • Currently participating in the original study (18001) and are:
    • Receiving treatment
    • In short-term follow-up
    • In long-term follow-up

Exclusion Criteria

  • Participated in the Phase 1b part of Study 18001.
  • Are pregnant or planning to become pregnant during the study or within 30 days after the last dose.
  • Intend to breastfeed during the study or within 1 week after the last dose.

Locations

FACILITYZIPCITYSTATE
Sylvester Comprehensive Cancer Center33136-1002MiamiFlorida
Florida Cancer Specialists34232-6422SarasotaFlorida
The Emory Clinic30322-1013AtlantaGeorgia
Northwestern University60611-3013ChicagoIllinois
Dana-Farber Cancer Institute02115BostonMassachusetts
Mayo Clinic- Minnesota55905RochesterMinnesota
University Of Nebraska Medical Center69198OmahaNebraska
Northwell Health11042-1118Lake SuccessNew York
Memorial Sloan-Kettering Cancer Center (MSKCC) - New York10065-6007New YorkNew York
Duke University Medical Center27710-4000DurhamNorth Carolina

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