FDA Approves Johnson & Johnson's RYBREVANT FASPRO for EGFR-Mutated NSCLC
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The FDA has approved Johnson & Johnson's RYBREVANT FASPRO for EGFR-mutated NSCLC, marking a significant advancement with its subcutaneous administration option. This approval offers a more convenient and faster alternative to intravenous delivery, supported by data showing unmatched overall survival benefits. The news was generated by Public Technologies using AI and is based on Johnson & Johnson's original content from December 17, 2025.
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