Master Rollover Protocol for Continued Safety Assessment of Study Drug
Available (expanded access)
Conditions studied: Cancer
In brief
This study is for patients who have participated in a previous study and who continue to receive benefit to have continued access to study drug and/or treatment.
Key facts
- Study ID
- NCT02632994
- Run by
- Eli Lilly and Company
- Last updated by the study team
- 2026-06-25
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- To be eligible patients must be currently receiving benefit in a concluded Lilly study for a compound that has opened an addendum in the continued access protocol.
You may not qualify if…
- Patients must not be concurrently enrolled in any other type of medical research judged not to be scientifically or medically compatible with this study.
Where it is running
- UCLA Medical Center — Torrance, California, United States
- Fort Wayne Oncology & Hematology — Fort Wayne, Indiana, United States
- Sarah Cannon Cancer Center — Nashville, Tennessee, United States
Full record on ClinicalTrials.gov
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