Breast Cancer Clinical Trial

A Study of LY3435151 in Participants With Solid Tumors

Summary

The reason for this study is to see if the study drug LY3435151 is safe in participants with advanced solid tumors.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Participant must have certain types of cancer, which your study doctor will discuss with you
Participant must have stopped other forms of treatment for cancer, which your study doctor will discuss with you
Participant must be able and willing to provide a sample of your tumor before beginning treatment and once while on treatment. For certain tumor types, the outcome of the biopsy may exclude you from the study treatment (for Phase 1b)
Participant must agree to use birth control
Participant must have progressed through or are intolerant to therapies with known clinical benefit, which your study doctor will discuss with you

Exclusion Criteria:

Participant must not have a history of tuberculosis, uncontrolled HIV or uncontrolled hepatitis B or C virus infection
Participant must not have an autoimmune disease, which your study doctor will discuss with you
Participant must not use corticosteroids, which your study doctor will discuss with you
Participant must not have heart disease, Crohn's disease or brain cancer
Participant must not be pregnant or breastfeeding

Study is for people with:

Breast Cancer

Phase:

Phase 1

Estimated Enrollment:

2

Study ID:

NCT04099277

Recruitment Status:

Terminated

Sponsor:

Eli Lilly and Company

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There are 2 Locations for this study

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University of Texas MD Anderson Cancer Center
Houston Texas, 77030, United States
National Cancer Center Hospital
Chuo-Ku Tokyo, 104-0, Japan

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 1

Estimated Enrollment:

2

Study ID:

NCT04099277

Recruitment Status:

Terminated

Sponsor:


Eli Lilly and Company

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