Study on the Long-Term Safety of Pirtobrutinib (LY3527727)

Sponsor: Eli Lilly and Company

Sponsor score: 60

ClinicalTrials ID:NCT06876649

This study is designed to monitor the long-term safety and effectiveness of the drug pirtobrutinib for participants who have completed earlier clinical trials involving this medication. Participants from these previous studies can continue their treatment or follow-up visits under this new study framework.

Patient Parameters

Program Overview

The purpose of this study is to evaluate the long-term safety and effectiveness of pirtobrutinib, a medication that has been tested in earlier clinical trials. Participants who were part of these previous studies can join this new study to continue receiving the medication or to have follow-up visits. This study combines information from different trials to provide a comprehensive understanding of pirtobrutinib's long-term effects.

Eligibility Criteria

Inclusion Criteria

  • Currently participating in a Lilly-sponsored clinical study that involves pirtobrutinib.

Exclusion Criteria

  • Pregnant or planning to become pregnant during the study or within 30 days after the last dose of the study treatment.
  • Breastfeeding during the study or within 1 week after the last dose of the study treatment.

Locations

FACILITYZIPCITYSTATE
University of California Medical Center94143-2204San FranciscoCalifornia
Sylvester Comprehensive Cancer Center33136-1002MiamiFlorida
Florida Cancer Specialists34232-6422SarasotaFlorida
The Emory Clinic30322-1013AtlantaGeorgia
Northwestern University60611-3013ChicagoIllinois
Dana-Farber Cancer Institute02215BostonMassachusetts
Mayo Clinic- Minnesota55905RochesterMinnesota
University Of Nebraska Medical Center69198OmahaNebraska
Northwell Health11042-1118Lake SuccessNew York
Memorial Sloan-Kettering Cancer Center (MSKCC) - New York10065-6007New YorkNew York

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