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Regeneron Pharmaceuticals (REGN) fell 2.44% on September 3, 2025, with a trading volume of $0.64 billion, ranking 144th in market activity. Recent developments highlight a mixed regulatory and strategic landscape for the biotech firm. The U.S. Food and Drug Administration (FDA) approved Linvoseltamab for multiple myeloma and extended review deadlines for two of Regeneron’s submissions, introducing uncertainty in its pipeline timelines. Positively, the company reported positive Phase III trial results for generalized myasthenia gravis, a rare neuromuscular disorder, which could strengthen its autoimmune portfolio. Analysts at
ISI maintained a "Buy" rating with a $750 price target, citing long-term potential in its bispecific antibody and gene therapy programs.Regeneron’s strategic collaborations, including partnerships with
and , remain central to its growth strategy. A 50-50 profit-sharing model on key programs like Libtayo and itepekimab has bolstered revenue streams, contributing $1.44 billion in collaboration revenue during Q2 2025. However, biosimilar pressures on its flagship EYLEA drug—down 25% year-to-date—highlight vulnerabilities in its ophthalmology segment. The company’s $7 billion investment in U.S. manufacturing and R&D underscores its focus on sustaining competitive advantages amid industry-wide pricing challenges.Shareholder returns and disciplined capital allocation also shaped recent investor sentiment.
returned $2.3 billion to shareholders in 2025 while expanding its genomic capabilities through acquisitions like Telesis Bio. Analysts project a 20%+ price appreciation, driven by Dupixent’s expansion into eight indications and Libtayo’s $1.2 billion market potential. Despite a 51.5% decline from its 52-week high, the stock’s forward P/E of 13.3x remains below the biotech industry average, suggesting undervaluation relative to fundamentals.Backtesting of historical performance indicates a projected intrinsic value of $1,544.16 per share, a 62.9% premium to the current price. This discrepancy reflects optimism around Regeneron’s genomic-driven pipeline and regulatory adaptability, though near-term volatility from FDA decisions and biosimilar competition may persist.

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