drugset / Trial / NCT04495478

A Study of Ramucirumab (LY3009806) in Healthy Participants

NCT04495478

Phase 1 Completed 50 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindBasic science

Summary

This study evaluates a new formulation of ramucirumab, a drug approved for several types of cancer. In this study of healthy participants, a small amount of ramucirumab will be given by injection either into a vein or just under the skin. Study doctors will measure the amount of ramucirumab in the bloodstream. Side effects and tolerability will be documented. The study will last for about 16 weeks for each participant, including screening and follow up. Screening is required within 28 days prior to entering the study.

Timeline

Start
2020-07-30
Primary completion
2021-05-09
Completion
2021-05-09

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ramucirumab Monoclonal antibody 350 mg Intravenous
Comparator Ramucirumab Monoclonal antibody 700 mg Intravenous

Indications

No indication recorded.