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WKN: 881535 | ISIN: US75886F1075 | Ticker-Symbol: RGO
Tradegate
21.02.25
17:50 Uhr
668,80 Euro
+6,00
+0,91 %
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REGENERON PHARMACEUTICALS INC Chart 1 Jahr
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REGENERON PHARMACEUTICALS INC 5-Tage-Chart
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17:18Price Over Earnings Overview: Regeneron Pharmaceuticals3
13:58Korean court rules in favor of Samsung Bioepis over Regeneron's Eylea3
DoDividendenbekanntmachungen (20.02.2025)4.284 Unternehmen  ISIN-Code  Dividende (Währung)  Dividende (EUR)  ADVANCED INFO SERVICE PCL  TH0268010Z11  5,74 THB  0,1632 EUR  ADVANCED INFO SERVICE PCL NVDR  TH0268010R11  5,74 THB  0,1632 EUR  ALUMASC...
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MiSanofi and Regeneron's Dupixent granted FDA priority review for bullous pemphigoid5
REGENERON PHARMACEUTICALS Aktie jetzt für 0€ handeln
DiRegeneron, Sanofi asthma therapy Dupixent under FDA review for rare skin condition4
DiFDA To Review Teva and Alvotech Drug That Could Compete With Regeneron's Eylea24
DiDupixent von Regeneron und Sanofi erhält bevorzuge US-Prüfung325DJ Dupixent von Regeneron und Sanofi erhält bevorzuge US-Prüfung Von Colin Kellaher DOW JONES--Der Entzündungshemmer Dupixent von Sanofi und Regeneron Pharmaceuticals könnte bald in einer neuen...
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DiSNY and REGN's Dupixent sBLA for Skin Disease Gets FDA's Priority Tag7
DiFDA to review Sanofi and Regeneron's Dupixent sBLA for bullous pemphigoid5
DiRegeneron & Sanofi: FDA Accepts Dupixent SBLA For Priority Review In Bullous Pemphigoid Treatment286PARIS (dpa-AFX) - The U.S. Food and Drug Administration has accepted for Priority Review the supplemental Biologics License Application or sBLA for Dupixent (dupilumab) to treat adults with...
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DiRegeneron Pharmaceuticals, Inc.: Dupixent (dupilumab) sBLA Accepted for FDA Priority Review for the Targeted Treatment of Bullous Pemphigoid (BP)124If approved, Dupixent would be the first and only targeted medicine to treat BP in the U.S.; FDA decision expected by June 20, 2025 Priority Review granted based on positive pivotal results demonstrating...
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SaHere's How Much You Would Have Made Owning Regeneron Pharmaceuticals Stock In The Last 15 Years19
12.02.FDA to review Regeneron's linvoseltamab BLA for multiple myeloma treatment9
11.02.Regeneron Pharma Says FDA Accepted BLA For Linvoseltamab To Treat Multiple Myeloma293 WASHINGTON (dpa-AFX) - Regeneron Pharmaceuticals, Inc. (REGN) Tuesday said that the resubmission of Biologics License Application (BLA) for linvoseltamab for the treatment of multiple myeloma...
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11.02.Regeneron multiple myeloma therapy accepted for FDA review12
11.02.Regeneron Pharmaceuticals, Inc.: Linvoseltamab BLA Accepted for FDA Review for the Treatment of Relapsed/Refractory Multiple Myeloma647Acceptance follows resolution of third-party fill/finish manufacturing issues FDA decision expected by July 10, 2025 TARRYTOWN, N.Y., Feb. 11, 2025 (GLOBE NEWSWIRE) -- Regeneron Pharmaceuticals,...
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09.02.Regeneron Announces Positive Phase 3 Results For EYLEA HD In Retinal Vein Occlusion Treatment554LEVERKUSEN (dpa-AFX) - Regeneron Pharmaceuticals Inc. (REGN) announced encouraging outcomes from the Phase 3 QUASAR trial, which evaluated the efficacy of EYLEA HD (aflibercept) Injection 8...
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09.02.Regeneron: EYLEA HD Shows Sustained Vision Gains In Wet AMD Patients At 3 Years530LEVERKUSEN (dpa-AFX) - Regeneron Pharmaceuticals Inc. (REGN) announced positive three-year (156-week) results for EYLEA HD (aflibercept) Injection 8 mg in patients with wet age-related macular...
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08.02.Regeneron Pharmaceuticals, Inc.: EYLEA HD (aflibercept) Injection 8 mg Positive Phase 3 Results in Patients with Macular Edema following Retinal Vein Occlusion Presented at Angiogenesis Meeting125TARRYTOWN, N.Y., Feb. 08, 2025 (GLOBE NEWSWIRE) -- Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) today announced the first presentation of positive results from the Phase 3 QUASAR trial investigating...
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08.02.Regeneron Pharmaceuticals, Inc.: Three-Year Results for EYLEA HD (aflibercept) Injection 8 mg in Patients with Wet Age-related Macular Degeneration Demonstrate Continued Durable Vision Gains and Anatomic Improvements with ...95At three years of EYLEA HD treatment, the vast majority of patients maintained visual and anatomic improvements while achieving extended dosing regimens, including those of just twice a year: 77%...
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