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Recruiting Phase 4 NCT06876649

A Master Protocol to Evaluate the Long-Term Safety of (LY3527727) Pirtobrutinib

Phase 4 – monitoring after market approval
Conditions: Chronic Lymphocytic Leukemia Non-Hodgkin Lymphoma

Sponsor: Eli Lilly and Company

trial.available_in: БГ
Overview
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.
Who can participate
Inclusion Criteria: * Are participating in an eligible Lilly sponsored clinical study evaluating pirtobrutinib. Exclusion Criteria: Exclusion criteria are defined in each ISA.
Locations 8
Australia (1)
Flinders Medical Centre
Adelaide
France (1)
CHU de Nantes - Hotel Dieu
Nantes
Italy (1)
IRCCS-AOU di Bologna-Policlinico S.Orsola-Malpighi
Bologna
Japan (1)
Nagoya Medical Center
Aichi-Ken
Poland (1)
Pratia MCM Krakow
Krakow
South Korea (1)
Seoul National University Hospital
Seoul
United Kingdom (1)
St James's University Hospital
Leeds
United States (1)
Cancer Specialists, LLC
Jacksonville , Florida
NOT_YET_RECRUITING
Technical details
Status
Recruiting
Phase
Phase 4
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
20.05.2025
Completion date
01.12.2032
Registry ID
NCT06876649
Source
anzctr
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