Johnson & Johnson's Mid-Stage Lung Cancer Trial Reveals Fewer Infusion-Related Reactions
Portfolio Pulse from Vandana Singh
Johnson & Johnson's Phase 2 SKIPPirr study shows a significant reduction in infusion-related reactions for Rybrevant in lung cancer patients. The Phase 3 MARIPOSA study also highlights improved survival rates with Rybrevant plus Lazcluze compared to osimertinib. The FDA approved Rybrevant plus Lazcluze as a first-line therapy for EGFR-mutated NSCLC.
September 11, 2024 | 1:08 pm
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Johnson & Johnson's Rybrevant shows reduced infusion-related reactions and improved survival rates in lung cancer trials. The FDA has approved Rybrevant plus Lazcluze as a first-line therapy for EGFR-mutated NSCLC, potentially boosting JNJ's market position.
The successful reduction in infusion-related reactions and improved survival rates in trials enhance the clinical profile of Rybrevant. FDA approval for Rybrevant plus Lazcluze as a first-line therapy for EGFR-mutated NSCLC is a significant regulatory milestone, likely to positively impact JNJ's stock price.
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IMPORTANCE 90
RELEVANCE 100