A Master Protocol to Evaluate the Long-Term Safety of (LY3527727) Pirtobrutinib
A Master Protocol to Evaluate the Long-Term Safety of Pirtobrutinib
Who can join
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 18 Years and older
- Sex
- All sexes
- Healthy volunteers
- Not accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
Not stated in the study description — ask the study team about visits and procedures.
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
The master protocol study J2N-MC-JZNY provides a framework to enable the evaluation of the long-term safety and efficacy of pirtobrutinib after completion of clinical studies evaluating pirtobrutinib. The clinical studies that will feed into this master protocol are referred to as originator studies. The master protocol will govern individual study-specific appendices (ISAs) that will represent participants from the individual, completed originator studies. These participants will have the opportunity to enter this study and continue to receive treatment or continue follow-up visits. Overall, the master protocol and the individual ISAs, when combined, define the investigations for this study.
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Official eligibility criteria
Inclusion Criteria: * Are participating in an eligible Lilly sponsored clinical study evaluating pirtobrutinib. Exclusion Criteria: Exclusion criteria are defined in each ISA.
Study sites (20)
FL
- Cancer Specialists, LLC · Jacksonville, FL 32256Ayed Ayed · Principal investigatorMore trials in Jacksonville
- Sylvester Comprehensive Cancer Center · Miami, FL 33136-1002 · Study contact · 954-265-6549Alvaro Alencar · Principal investigatorMore trials in Miami
- Florida Cancer Specialists · Sarasota, FL 34232-6422 · Study contact · 941-377-9993Manish Patel · Principal investigatorMore trials in Sarasota
GA
- The Emory Clinic · Atlanta, GA 30322-1013 · Study contact · 404-778-3708Jonathon Cohen · Principal investigatorMore trials in Atlanta
IL
- Northwestern University · Chicago, IL 60611-3013 · Study contact · 60611-3013Shuo Ma · Principal investigatorMore trials in Chicago
MA
- Dana-Farber Cancer Institute · Boston, MA 02215 · Study contact · 617-632-5847Jennifer Brown · Principal investigatorMore trials in Boston
MN
- Mayo Clinic- Minnesota · Rochester, MN 55905 · Study contact · 507-284-2511Yucai Wang · Principal investigatorMore trials in Rochester
NC
- Duke University Medical Center · Durham, NC 27710-4000 · Study contact · 919-684-8111Matthew McKinney · Principal investigatorMore trials in Durham
NE
- University Of Nebraska Medical Center · Omaha, NE 69198 · Study contact · 402-559-5166Matthew Lunning · Principal investigatorMore trials in Omaha
NY
- Cayuga Cancer Center · Ithaca, NY 14850 · Study contact · 607-272-5414Cynthia Davis · Principal investigatorMore trials in Ithaca
- Northwell Health · Lake Success, NY 11042-1118 · Study contact · 516-734-8959Steven Allen · Principal investigatorMore trials in Lake Success
- Memorial Sloan-Kettering Cancer Center (MSKCC) - New York · New York, NY 10065-6007 · Study contact · 646-608-4273Prioty Islam · Principal investigatorMore trials in New York
- Memorial Sloan-Kettering Cancer Center (MSKCC) - New York · New York, NY 10065-6007 · Study contact · 646-608-4273Prioty Islam · Principal investigatorMore trials in New York
- Memorial Sloan-Kettering Cancer Center (MSKCC) - New York · New York, NY 10065-6007Prioty Islam · Principal investigatorMore trials in New York
OH
- Ohio State University Comprehensive Cancer Center · Columbus, OH 43210-1063 · Study contact · 614-293-3196Jennifer Woyach · Principal investigatorMore trials in Columbus
PA
- University of Pennsylvania Hospital · Philadelphia, PA 19104 · Study contact · 215-662-3933Sunita Nasta · Principal investigatorMore trials in Philadelphia
TN
- Tennessee Oncology · Nashville, TN 37203-2659 · Study contact · 615-524-4074Michael Byrne · Principal investigatorMore trials in Nashville
TX
- University of Texas MD Anderson Cancer Center · Houston, TX 77030 · Study contact · 713-792-2860Michael Wang · Principal investigatorMore trials in Houston
WA
- Swedish Cancer Institute · Seattle, WA 98104-3588 · Study contact · 98104-3588Swathi Namburi · Principal investigatorMore trials in Seattle
WI
- Medical College of Wisconsin · Milwaukee, WI 53226-3548 · Study contact · 414-805-4600Nirav Shah · Principal investigatorMore trials in Milwaukee