YONSA (abiraterone acetate) by Fosun Pharma is abiraterone, an androgen biosynthesis inhibitor, that inhibits 17 α-hydroxylase/c17,20-lyase (cyp17). First approved in 2018.
Drug data last refreshed 2h ago · AI intelligence enriched 1w ago
YONSA (abiraterone acetate) is an oral small molecule androgen biosynthesis inhibitor that blocks CYP17 enzyme to reduce testosterone production in castration-resistant prostate cancer (CRPC). It inhibits androgen production in testicular, adrenal, and tumor tissues, addressing the unmet need for patients whose cancer progresses despite GnRH agonist or orchiectomy treatment. The drug was approved in 2018 and represents a key component of hormonal therapy in advanced prostate cancer management.
Product is in peak commercial phase with stable Medicare utilization; oncology teams are likely operating at mature efficiency rather than growth mode.
abiraterone, an androgen biosynthesis inhibitor, that inhibits 17 α-hydroxylase/C17,20-lyase (CYP17). This enzyme is expressed in testicular, adrenal, and prostatic tumor tissues and is required for androgen biosynthesis. CYP17 catalyzes two sequential reactions: 1) the conversion of pregnenolone…
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
A Study of Talazoparib With or Without Enzalutamide in People With Prostate Cancer Who Have Previously Received Abiraterone Acetate
Niraparib, Abiraterone Acetate and Prednisone for mHSPC With Deleterious Homologous Recombination Repair Alterations
Race Impact on Efficacy of Niraparib Plus Abiraterone Acetate and Prednisone in Patients With Homologous Repair Deficient Castration-resistant Prostate Cancer
REVELUTION-2: Relugolix+Abiraterone Acetate (AA) Versus Leuprolide+AA Cardiac Trial
A Study to Learn About the Investigational Medicine Called PF-06821497 (Mevrometostat) in Men With mCRPC Who Were Previously Treated With Abiraterone Acetate for Prostate Cancer (MEVPRO-1).
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Upgrade to Pro — $25/moYONSA positions professionals in a mature, profitable oncology asset with established market presence and patient populations, offering stable career footing within a competitive CRPC landscape. With 7.9 years until LOE, roles on this product provide medium-term opportunity but require transition planning toward growth assets or LOE mitigation strategies by 2030.