NCT04792463: Frequency and Clinical Phenotype of BAP1 Hereditary Predisposition Syndrome

Breast Cancer Type: HER2+, HR+ & HER2-negative, Triple Negative
Hormone Mutations: ER+, PR+
Other Mutations: DNA damage repair mutations
Breast Cancer Tissue: 
Recruitment Status: Recruiting

Drug Category: Other

Key Eligibility Criteria:

Gender: All
Age: Child, Adult, Older Adult
Location of Metastases: 
Additional Notes: Patient or family member must have a BAP1 hereditary mutation or variant of uncertain significance

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