U.S. FDA Approval of RYBREVANT FASPRO™ (amivantamab and hyaluronidase-lpuj) Enables the Simplest, Shortest Administration Time for a First-Line Combination Regimen when Combined with LAZCL...
Johnson & Johnson (JNJ)
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Source: Yahoo! Finance
Approval builds on previously reported Phase 3 MARIPOSA data showing unmatched overall survival benefit of this chemotherapy-free regimen, projected to exceed four years HORSHAM, Pa. Dec. 17, 2025 /PRNewswire/ -- Johnson & Johnson (NYSE: JNJ) announced today that the U.S. Food and Drug Administration (FDA) approved RYBREVANT FASPRO ™ (amivantamab and hyaluronidase-lpuj), the first and only subcutaneously (SC) administered therapy for patients with epidermal growth factor receptor (EGFR)-mutated non-small cell lung cancer (NSCLC). RYBREVANT FASPRO ™ is approved across all indications of RYBREVANT ® (amivantamab-vmjw). Experience the full interactive Multichannel News Release here: https://www.multivu.com/johnson-and-johnson/9361151-en-johnson-and-johnson-us-fda-approval-rybrevant-faspro-amivantamab-and-hyaluronidase-lpuj Compared to intravenous (IV) delivery, RYBREVANT FASPRO ™ offers significantly higher patient convenience and lower burden on healthcare resources Reducing ad
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News
- U.S. FDA Approval of RYBREVANT FASPRO™ (amivantamab and hyaluronidase-lpuj) Enables the Simplest, Shortest Administration Time for a First-Line Combination Regimen when Combined with LAZCLUZE® (lazertinib)PR Newswire
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JNJ
Earnings
- 10/14/25 - Beat
JNJ
Sec Filings
- 12/11/25 - Form 4
- 12/11/25 - Form 4
- 12/11/25 - Form 4
- JNJ's page on the SEC website