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VisitLeading company in NSCLC treatment innovation by end of 2025?
Novocure • 25%
AstraZeneca • 25%
Chinese Biotech Firms • 25%
Other • 25%
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FDA Approves Novocure's Optune Lua for Metastatic NSCLC with PD-1/PD-L1 Inhibitors, Based on LUNAR Study
Oct 15, 2024, 08:09 PM
The FDA has approved Novocure's Optune Lua for concurrent use with PD-1/PD-L1 inhibitors or docetaxel in treating metastatic non-small cell lung cancer (mNSCLC) for patients who have progressed on or after a platinum-based regimen. This approval, announced on October 15, is based on the LUNAR study, which demonstrated a statistically significant improvement in overall survival (OS). Additionally, sunvozertinib has received Breakthrough Therapy Designation in China for treatment-naive EGFR Exon 20+ non-small cell lung cancer (NSCLC) as of October 14. Furthermore, the FDA has approved durvalumab with platinum-containing chemotherapy as neoadjuvant treatment, followed by single-agent durvalumab as adjuvant treatment after surgery for adults with resectable NSCLC.
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Pfizer • 25%
Roche • 25%
AstraZeneca • 25%
Other • 25%
Merck & Co. • 25%
AstraZeneca • 25%
Roche • 25%
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Johnson & Johnson • 25%
Pfizer • 25%
AstraZeneca • 25%
Roche • 25%
Summit Therapeutics' ivonescimab • 25%
Merck's Keytruda • 25%
Roche's Tecentriq • 25%
Other • 25%
Merck • 25%
Roche • 25%
Another Pharmaceutical Company • 25%
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iTeos Therapeutics • 25%
GSK • 25%
Another company • 25%
No approval by end of 2025 • 25%
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Pfizer • 25%
Novartis • 25%
Roche • 25%
Other • 25%
Asia • 25%
Africa • 25%
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