熱門資訊> 正文
FDA接受ozeikibart的Inhibrx BLA
2026-06-15 22:34
- The US FDA has accepted for review Inhibrx Biosciences' (INBX) BLA for ozekibart to treat unresectable or metastatic conventional chondrosarcoma.
- The application has an action date of April 14, 2027.
- There are currently no FDA-approved therapies for the rare bone cancer.
- The BLA is supported by data from the ChonDRAgon study that met its primary endpoint of a statistically significant median progression-free survival for individuals given ozekibart compared to placebo.
- Ozekibart is considered a tetravalent death receptor 5 (DR5) agonist antibody.
More on Inhibrx Biosciences
- Inhibrx: Spinoff Rumors Send Shares Soaring - Stunning Bull Run Can Continue
- Inhibrx Biosciences FY25 Review: Catalyst-Driven Hold Ahead Of Key 2026 Data
- Inhibrx Biosciences GAAP EPS of -$2.15
- Inhibrx rises on upcoming interim mid-stage data for head and neck cancer asset
- Seeking Alpha’s Quant Rating on Inhibrx Biosciences
風險及免責提示:以上內容僅代表作者的個人立場和觀點,不代表華盛的任何立場,華盛亦無法證實上述內容的真實性、準確性和原創性。投資者在做出任何投資決定前,應結合自身情況,考慮投資產品的風險。必要時,請諮詢專業投資顧問的意見。華盛不提供任何投資建議,對此亦不做任何承諾和保證。