A Study of LOXO-783 in Patients With Breast Cancer/Other Solid Tumors
About the study
Who can take part
INCLUSION CRITERIA
Inclusion Criteria:
- Have advanced breast cancer or another solid tumor with the presence of a phosphatidylinositol 3-kinase catalytic subunit alpha (PIK3CA) H1047R mutation (or other Sponsor and safety review committee (SRC)-approved, activating PIK3CA mutations other than H1047R mutation)
- Have adequate archival tumor tissue sample available or be approved by the Sponsor for enrollment if no tumor sample is available.
- Have stopped all cancer treatment and have recovered from the major side effects
- Have adequate organ function, as measured by blood tests
- Have a performance status of 0 or 1 on the Eastern Cooperative Oncology Group (ECOG) scale
Patients must have
Measurable disease
--- Patients with non-breast tumor types must have at least 1 measurable lesion
Non-measurable bone disease (at least 1 bone lesion in breast cancer patients only)
For patients with an estrogen receptor (ER)+ breast cancer diagnosis:
- If female, must be postmenopausal
- If male, must agree to use hormone suppression
Phase 1a:
-- Dose escalation and backfill patients:
- Advanced solid tumor
- Patients may have had up to 5 prior regimens for advanced disease
Phase 1b:
Part A:
- ER+/human epidermal growth factor receptor 2 (HER2)- advanced breast cancer
- Patients may have had up to 5 prior regimens for advanced disease ---- Prior cyclin dependent kinase (CDK)4/6 inhibitor therapy required
Part B:
- ER+/HER2- advanced breast cancer
- Patients may have had up to 2 prior regimens for advanced disease.
Part C:
ER+/HER2- advanced breast cancer
Patients may have had up to 5 prior regimens for advanced disease.
---- Prior CDK4/6 inhibitor therapy required.
Have a diagnosis of diabetes mellitus Type 2
Part D:
- Advanced breast cancer
- Patients may have had up to 5 prior regimens for advanced disease.
Part E:
- Advanced solid tumor
- Patients may have had up to 3 prior regimens for advanced disease advanced disease
Part F:
ER+/HER2- advanced breast cancer
Patients may have had up to 5 prior regimens for advanced disease
Prior cyclin dependent kinase (CDK)4/6 inhibitor therapy required
EXCLUSION CRITERIA
Exclusion Criteria:
Medical Conditions
- Colorectal cancer
- Endometrial cancers with specific concurrent oncogenic alterations
A history of known active or suspected
- Diabetes mellitus Type 1 or
- Diabetes mellitus Type 2 requiring antidiabetic medication (Phase 1a and all parts of Phase 1b except Part C).
- Serious concomitant systemic disorder
- Known or suspected history of untreated or uncontrolled central nervous system (CNS) involvement.
- Active uncontrolled systemic bacterial, viral, fungal, or parasitic infection, or other clinically significant active disease process
- Prior exposure to phosphatidylinositol 3-kinase/protein kinase B/mammalian target of rapamycin (PI3K/AKT/mTOR) inhibitor(s), except in certain circumstances
Study Locations
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How to Apply
Study’s details
Contition
Breast Cancer
Age (in years)
18+
Phase
Phase 1
Participants needed
400
Est. Completion Date
May 31, 2025
Treatment type
Interventional
Sponsor
Eli Lilly and Company
ClinicalTrials.gov identifier
NCT05307705
Study number
LOXO-PIK-21001
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