Genentech’s Tecentriq Receives the US FDA’s Approval as Adjuvant Treatment for Early Non-Small Cell Lung Cancer

October 18, 2021 Auto Bot approval, FDA, Genentech, Non-Small Cell Lung Cancer, regulatory, Tecentriq 0

Shots:

  • The approval is based on P-III IMpower010 study Tecentriq vs BSC in 1005 patients in a ratio (1:1) with Stage IB-IIIA NSCLC, following surgical resection and up to 4 cycles of adjuvant cisplatin-based CT
  • The results showed a 34% reduction in risk of disease recurrence or death in people with Stage II-IIIA NSCLC whose tumors express PD-L1≥1%, safety data were consistent with known safety profile & no new safety signals were observed
  • The FDA has reviewed & approved the supplemental application under the RTOR program for safe & effective treatments to patients imminently. The company has an extensive program for Tecentriq including ongoing & planned P-III studies for multiple cancers

Click here to­ read the full press release/ article | Ref: Businesswire | Image: Xconomy

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