Master Rollover Protocol for Continued Safety Assessment of Study Drug
ConditionCancer
Trial statusAvailable
Trial phaseNot listed
Trial typeExpanded Access
Biological sexAll
Age18+
SponsorEli Lilly and Company
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.
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.
Patients must not be concurrently enrolled in any other type of medical research judged not to be scientifically or medically compatible with this study.