Drug data last refreshed Yesterday · AI intelligence enriched 2w ago
VIJOICE (alpelisib) is an oral small-molecule PI3K inhibitor approved in 2022 for multiple oncology and rare genetic indications. It treats PIK3CA-driven cancers including breast cancer, ovarian cancer, endometrial cancer, and rare conditions like PIK3CA-related overgrowth spectrum and lymphatic malformations. The drug works by selectively inhibiting phosphatidylinositol 3-kinase (PI3K), blocking a key growth pathway in PIK3CA-mutated tumors.
Product is at peak lifecycle with modest Part D spending, indicating early commercialization phase with growth potential in rare disease and oncology segments.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
EPIK-P4: A Phase II Single-arm Study to Assess the Efficacy, Safety and Pharmacokinetics of Alpelisib (BYL719) in Pediatric and Adult Patients With PIK3CA-related Overgrowth Spectrum (PROS)
24VA022; VATCH Alpelisib for TIE2/PIK3CA Pathway VAs
A Study of Alpelisib and Fulvestrant to Treat Endometrial Cancer
Alpelisib in Pediatric and Adult Patients With Lymphatic Malformations Associated With a PIK3CA Mutation.
Detection of Tumor DNA in the Blood of Patients Receiving Standard Therapy for Hormone Receptor-positive (HR+) Non-HER2 Expressing (HER2-) Metastatic Breast Cancer as a Tool to Select Those Who May Benefit From the Next Course of Fulvestrant in Combination With Alpelisib or Ribociclib
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Upgrade to Pro — $25/moNovartis is hiring 7 roles related to this product
Nine linked positions reflect early-to-mid lifecycle commercial stage with emphasis on regulatory navigation, manufacturing scale-up, and quality oversight. Roles skew toward operational and regulatory functions rather than peak-stage commercial maximization, indicating ongoing development and compliance work.
9 open roles linked to this drug