A Study of LY3295668 Erbumine in Participants With Breast Cancer That Has Spread to Other Parts of the Body
Completed · Phase 1
Conditions studied: Metastatic Breast Cancer
In brief
The reason for this study is to determine the recommended phase 2 dose of the study drug LY3295668 erbumine in participants with breast cancer that has spread to other parts of the body.
Key facts
- Study ID
- NCT03955939
- Run by
- Eli Lilly and Company
- People needed
- 5
- Starts
- 2019-08-02
- Expected to finish
- 2020-05-14
- Last updated by the study team
- 2020-06-01
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Participant must have hormone receptor positive and HER2 negative metastatic breast cancer
- Participant must have progressed on at least 1 line of endocrine therapy and 1 cyclin dependent kinase (CDK)4/6 inhibitor
- Participant must be able and willing to undergo mandatory tumor biopsy
- Participant must have normal organ function
- Participant must be able to swallow capsules
You may not qualify if…
- Participant must not have had prior chemotherapy for mBC. Chemotherapy in the adjuvant/neoadjuvant setting is permitted
- Participant must not be currently enrolled in a clinical study
- Participant must not have another serious medical condition
- Participant must not have previously received an aurora kinase inhibitor
Where it is running
- City of Hope National Medical Center — Duarte, California, United States
- Dana Farber Cancer Institute — Boston, Massachusetts, United States
- South Texas Accelerated Research Therapeutics, LLC — San Antonio, Texas, United States
- Cliniques Universitaires Saint-Luc — Brussels, Belgium
- Universitair Ziekenhuis Antwerpen — Edegem, Belgium
- Universitair Ziekenhuis Gent — Ghent, Belgium
- Universitaire Ziekenhuizen Leuven - Campus Gasthuisberg — Leuven, Belgium
Full record on ClinicalTrials.gov
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