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Regeneron Pharmaceuticals, Inc. (REGN34.SA)

São Paulo - São Paulo Delayed price. Currency in BRL
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78.390.00 (0.00%)
As of 03:47PM BRT. Market open.
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Previous close78.39
Open0.00
Bid76.08 x N/A
Ask76.35 x N/A
Day's range78.39 - 78.39
52-week range55.99 - 81.52
Volume0
Avg. volume339
Market cap516.254B
Beta (5Y monthly)0.14
PE ratio (TTM)26.39
EPS (TTM)2.97
Earnings dateN/A
Forward dividend & yieldN/A (N/A)
Ex-dividend dateN/A
1y target estN/A
  • Reuters

    UPDATE 1-AbbVie's skin disease drug found to be more effective than Regeneron's Dupixent in study

    AbbVie said on Thursday its drug, Rinvoq, for treating a type of inflammatory skin condition was found to be more effective than Regeneron Pharmaceuticals and Sanofi's Dupixent in a late-stage head-to-head study. Rinvoq helped 19.9% of patients simultaneously achieve near-complete skin clearance with a no-to-little itch after 16 weeks of treatment, compared with 8.9% of patients treated with Dupixent, the study showed. The study is the first head-to-head trial in adults and adolescents with moderate-to-severe atopic dermatitis and had shown an inadequate response to systemic therapy, AbbVie said.

  • Zacks

    The Zacks Analyst Blog Highlights Danaher, Regeneron Pharmaceuticals, Palo Alto Networks, Workday and American Electric Power

    Danaher, Regeneron Pharmaceuticals, Palo Alto Networks, Workday and American Electric Power are part of the Zacks top Analyst Blog.

  • Reuters

    Regeneron to collaborate on gene editing therapies with Doudna-founded Mammoth

    Regeneron Pharmaceuticals and Mammoth Biosciences will collaborate to research, develop and commercialize gene editing therapies for multiple diseases, the companies said on Thursday. Mammoth's CRISPR-based gene editing platform and Regeneron's delivery technologies will be used to create disease-modifying medicines that can be delivered to tissues beyond the liver. CRISPR, discovered by Jennifer Doudna and CRISPR Therapeutics co-founder Emmanuelle Charpentier, uses molecular "scissors" to trim faulty parts of genes that can then be disabled or replaced with new strands of normal DNA.