Clinical Trial Detail

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NCT ID NCT04726332
Title Study of XL102 as Single-Agent and Combination Therapy in Subjects With Solid Tumors
Recruitment Recruiting
Gender both
Phase Phase I
Variant Requirements No
Sponsors Exelixis
Indications

Her2-receptor negative breast cancer

peritoneum cancer

prostate adenocarcinoma

triple-receptor negative breast cancer

ovary epithelial cancer

fallopian tube cancer

Advanced Solid Tumor

Therapies

Abiraterone + Prednisone + XL102

Fulvestrant + XL102

XL102

Age Groups: senior | adult
Covered Countries USA


No variant requirements are available.