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Spots Global Cancer Trial Database for Master Rollover Protocol for Continued Safety Assessment of Study Drug

The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Master Rollover Protocol for Continued Safety Assessment of Study Drug

Official Title: Master Rollover Protocol for Continued Safety Assessment of Study Drug

Study ID: NCT02632994

Conditions

Cancer

Interventions

LY2503029
LY3023414

Study Description

Brief Summary: 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.

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

UCLA Medical Center, Torrance, California, United States

Fort Wayne Oncology & Hematology, Fort Wayne, Indiana, United States

Sarah Cannon Cancer Center, Nashville, Tennessee, United States

Contact Details

Name: Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT -5 hours, EST)

Affiliation: Eli Lilly and Company

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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