Takeda’s Alunbrig (brigatinib) Receives the US FDA’s Priority Review to Treat ALK + Metastatic Non-Small Cell Lung Cancer
Shots:
- The US FDA has granted PR to Takeda’s sNDA for the expanded use of Alunbrig (brigatinib) as 1L treatment for patients with ALK+ metastatic NSCLC detected by FDA-approved test
- The sNDA is based on P-III ALTA-1L study assessing the Alunbrig (180mg qd with 7days preparatory phase to 90mg qd) vs crizotinib (bid) in 275 patients with LA/m-NSCLC, prior not treated with ALK inhibitor. The study resulted in meeting its 1EPs i.e, superiority in PFS
- Alunbrig is a news generation ITK inhibitor targeting genetic alterations in ALK with its anticipated PDUFA date as Jun 23, 2020
Click here to read full press release/ article | Ref: Business wire | Image: Takeda