Cancer Clinical Trial
Official title:
Master Rollover Protocol for Continued Safety Assessment of Study Drug
| NCT number | NCT02632994 |
| Other study ID # | 16161 |
| Secondary ID | I8I-MC-JYAA |
| Status | Available |
| Phase | |
| First received | |
| Last updated |
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.
| Status | Available |
| Enrollment | 0 |
| Est. completion date | |
| Est. primary completion date | |
| Accepts healthy volunteers | |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | Inclusion Criteria: - 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. Exclusion Criteria: - Patients must not be concurrently enrolled in any other type of medical research judged not to be scientifically or medically compatible with this study. |
| Country | Name | City | State |
|---|---|---|---|
| United States | Fort Wayne Oncology & Hematology | Fort Wayne | Indiana |
| United States | Sarah Cannon Cancer Center | Nashville | Tennessee |
| United States | UCLA Medical Center | Torrance | California |
| Lead Sponsor | Collaborator |
|---|---|
| Eli Lilly and Company |
United States,
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