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Regeneron Pharmaceuticals, Inc.

Regeneron Pharmaceuticals, Inc.

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REGENERON ANNOUNCES INVESTOR CONFERENCE PRESENTATIONS

11-02-2026
TARRYTOWN, N.Y., FEB. 11, 2026 (GLOBE NEWSWIRE) -- REGENERON PHARMACEUTICALS, INC. (NASDAQ: REGN) W...

REGENERON HIGHLIGHTS EXPANDING IMMUNOLOGY PORTFOLIO AND PIPELINE AT AAAAI, SHOWCASING NOVEL APPROACHES TO TREATING ALLERGY

10-02-2026
36 ABSTRACTS TO BE PRESENTED ACROSS REGENERON-INVENTED THERAPIES, INCLUDING FIRST-TIME PHASE 3 PRESE...

EYLEA HD® (AFLIBERCEPT) INJECTION 8 MG PRESENTATIONS AT ANGIOGENESIS 2026 UNDERSCORE STRENGTH OF ITS CLINICAL PROFILE FOR THE TREATMENT OF SERIOUS RETINAL DISEASES

02-02-2026
NEW PRESENTATIONS INCLUDE FINAL 64-WEEK RESULTS FROM THE PHASE 3 QUASAR TRIAL IN PATIENTS WITH RETIN...

REGENERON REPORTS FOURTH QUARTER AND FULL YEAR 2025 FINANCIAL AND OPERATING RESULTS

30-01-2026
TARRYTOWN, N.Y., JAN. 30, 2026 (GLOBE NEWSWIRE) -- REGENERON PHARMACEUTICALS, INC. (NASDAQ: REGN) TO...

NATION'S TOP 40 HIGH SCHOOL SCIENTISTS TO COMPETE FOR $1.8 MILLION IN AWARDS AT THE PRESTIGIOUS REGENERON SCIENCE TALENT SEARCH

21-01-2026
SOCIETY FOR SCIENCE & REGENERON ANNOUNCED THE FINALISTS IN THE REGENERON SCIENCE TALENT SEARCH, THE ...

DUPIXENT® (DUPILUMAB) APPROVED IN JAPAN FOR CHILDREN AGED 6 TO 11 YEARS WITH BRONCHIAL ASTHMA

23-12-2025
APPROVAL BASED ON GLOBAL PHASE 3 PROGRAM IN CHILDREN DEMONSTRATING DUPIXENT SIGNIFICANTLY REDUCED EX...

REGENERON ANNOUNCES PRESENTATION AT THE 44TH ANNUAL J.P. MORGAN HEALTHCARE CONFERENCE

22-12-2025
TARRYTOWN, N.Y., DEC. 22, 2025 (GLOBE NEWSWIRE) -- REGENERON PHARMACEUTICALS, INC. (NASDAQ: REGN) W...

LYNOZYFIC™ (LINVOSELTAMAB) MONOTHERAPY IN NEWLY DIAGNOSED MULTIPLE MYELOMA (NDMM) SHOWS IMPRESSIVE RESPONSES, SUPPORTING RATIONALE AS A POTENTIAL FOUNDATION IN FRONTLINE TREATMENT

07-12-2025
ALL THREE DOSE GROUPS (50 MG, 100 MG AND 200 MG) SHOWED IMPRESSIVE MONOTHERAPY EFFICACY, WITH VGPR+ ...

REGENERON AND TESSERA THERAPEUTICS TO JOINTLY DEVELOP TSRA-196, AN INVESTIGATIONAL GENE EDITING THERAPY FOR ALPHA-1 ANTITRYPSIN DEFICIENCY (AATD)

01-12-2025
TARRYTOWN, N.Y. AND SOMERVILLE, MASS., DEC. 01, 2025 (GLOBE NEWSWIRE) -- REGENERON PHARMACEUTICALS, ...

PRESS RELEASE: SANOFI AND REGENERON'S DUPIXENT APPROVED AS THE FIRST TARGETED MEDICINE IN THE EU IN OVER A DECADE FOR CHRONIC SPONTANEOUS URTICARIA

25-11-2025
SANOFI AND REGENERON'S DUPIXENT APPROVED AS THE FIRST TARGETED MEDICINE IN THE EU IN OVER A DECADE F...

EYLEA HD® (AFLIBERCEPT) INJECTION 8 MG APPROVED BY FDA FOR THE TREATMENT OF MACULAR EDEMA FOLLOWING RETINAL VEIN OCCLUSION (RVO) AND FOR MONTHLY DOSING ACROSS APPROVED INDICATIONS

19-11-2025
FIRST AND ONLY FDA-APPROVED TREATMENT  FOR RVO INDICATED FOR UP TO EVERY 8-WEEK DOSING AFTER AN INI...

LIBTAYO® (CEMIPLIMAB) APPROVED IN THE EUROPEAN UNION AS FIRST AND ONLY IMMUNOTHERAPY FOR ADJUVANT TREATMENT OF CUTANEOUS SQUAMOUS CELL CARCINOMA (CSCC) WITH HIGH RISK OF RECURRENCE AFTER SURGERY AND RADIATION

19-11-2025
APPROVAL BASED ON RESULTS OF LANDMARK PHASE 3 C-POST TRIAL THAT SHOW LIBTAYO IS FIRST IMMUNOTHERAPY ...

REGENERON HIGHLIGHTS PROGRESS AT AMERICAN SOCIETY OF HEMATOLOGY (ASH), WITH UPDATED DATA IN MULTIPLE MYELOMA, LYMPHOMA AND PAROXYSMAL NOCTURNAL HEMOGLOBINURIA PROGRAMS

13-11-2025
ORAL PRESENTATION OF LYNOZYFIC™ (LINVOSELTAMAB-GCPT) DATA IN NEWLY DIAGNOSED MULTIPLE MYELOMA FROM...

PRESS RELEASE: ACAAI: SANOFI AND REGENERON'S DUPIXENT PIVOTAL STUDY MET ALL PRIMARY AND SECONDARY ENDPOINTS, REDUCING SIGNS AND SYMPTOMS OF ALLERGIC FUNGAL RHINOSINUSITIS; SBLA ACCEPTED FOR FDA PRIORITY REVIEW

07-11-2025
ACAAI: SANOFI AND REGENERON'S DUPIXENT PIVOTAL STUDY MET ALL PRIMARY AND SECONDARY ENDPOINTS, REDUCI...

REGENERON ANNOUNCES INVESTOR CONFERENCE PRESENTATIONS

03-11-2025
TARRYTOWN, N.Y., NOV. 03, 2025 (GLOBE NEWSWIRE) -- REGENERON PHARMACEUTICALS, INC. (NASDAQ: REGN) W...

DUPIXENT® (DUPILUMAB) WINS PRESTIGIOUS 2025 PRIX GALIEN USA BEST BIOTECHNOLOGY PRODUCT AWARD

31-10-2025
AWARD RECOGNIZES THE GROUNDBREAKING SCIENCE OF DUPIXENT AND ITS TRANSFORMATIONAL IMPACT ON MULTIPLE ...

REGENERON REPORTS THIRD QUARTER 2025 FINANCIAL AND OPERATING RESULTS

28-10-2025
TARRYTOWN, N.Y., OCT. 28, 2025 (GLOBE NEWSWIRE) -- REGENERON PHARMACEUTICALS, INC. (NASDAQ: REGN) TO...

LIBTAYO® (CEMIPLIMAB) RECOMMENDED FOR EU APPROVAL BY THE CHMP FOR ADJUVANT TREATMENT OF CUTANEOUS SQUAMOUS CELL CARCINOMA (CSCC) WITH A HIGH RISK OF RECURRENCE AFTER SURGERY AND RADIATION

17-10-2025
POSITIVE OPINION BASED ON RESULTS OF PHASE 3 C-POST TRIAL THAT SHOW LIBTAYO SIGNIFICANTLY REDUCED TH...

REGENERON SHOWCASES ADVANCES ACROSS ONCOLOGY PORTFOLIO AND PIPELINE AT ESMO, HIGHLIGHTING NOVEL AND PATIENT-FOCUSED APPROACH FOR DIFFICULT-TO-TREAT CANCERS

15-10-2025
NEW SAFETY AND PHARMACOKINETIC DATA FROM PHASE 3 C-POST TRIAL PROVIDE INSIGHTS ON AN EVERY 6-WEEK DO...

DB-OTO RESULTS IN THE NEW ENGLAND JOURNAL OF MEDICINE SHOWCASE DRAMATIC AND SUSTAINED IMPROVEMENTS IN HEARING AND SPEECH PERCEPTION IN CHILDREN WITH PROFOUND GENETIC HEARING LOSS

12-10-2025
NEARLY ALL PARTICIPANTS (11 OF 12) EXPERIENCED CLINICALLY MEANINGFUL HEARING IMPROVEMENTS, INCLUDING...

LIBTAYO® (CEMIPLIMAB-RWLC) APPROVED IN THE U.S. AS FIRST AND ONLY IMMUNOTHERAPY FOR ADJUVANT TREATMENT OF CUTANEOUS SQUAMOUS CELL CARCINOMA (CSCC) WITH A HIGH RISK OF RECURRENCE AFTER SURGERY AND RADIATION

08-10-2025
APPROVAL BASED ON PIVOTAL PHASE 3 C-POST TRIAL SHOWING LIBTAYO SIGNIFICANTLY REDUCED THE RISK OF DIS...

REGENERON TO REPORT THIRD QUARTER 2025 FINANCIAL AND OPERATING RESULTS AND HOST CONFERENCE CALL AND WEBCAST ON OCTOBER 28, 2025

30-09-2025
TARRYTOWN, N.Y., SEPT. 30, 2025 (GLOBE NEWSWIRE) -- REGENERON PHARMACEUTICALS, INC. (NASDAQ: REGN) T...

EVKEEZA® (EVINACUMAB-DGNB) ANGPTL3 ANTIBODY APPROVED IN THE U.S. FOR CHILDREN AS YOUNG AS 1 YEAR OLD WITH ULTRA-RARE FORM OF HIGH CHOLESTEROL

26-09-2025
FDA APPROVAL EXTENDS THE INDICATION OF EVKEEZA TO TREAT YOUNGER PATIENTS WITH HOMOZYGOUS HYPERCHOLES...

PRESS RELEASE: SANOFI AND REGENERON'S DUPIXENT TO TREAT CHRONIC SPONTANEOUS URTICARIA ADVANCES IN EU WITH POSITIVE CHMP OPINION

22-09-2025
SANOFI AND REGENERON'S DUPIXENT TO TREAT CHRONIC SPONTANEOUS URTICARIA ADVANCES IN EU WITH POSITIVE ...

DUPIXENT® (DUPILUMAB) TO TREAT CHRONIC SPONTANEOUS URTICARIA (CSU) ADVANCES IN EU WITH POSITIVE CHMP OPINION

22-09-2025
RECOMMENDATION FOR ADULTS AND ADOLESCENTS BASED ON PHASE 3 TRIALS SHOWING DUPIXENT SIGNIFICANTLY RED...

REGENERON DONATES EBOLA TREATMENT FOR USE IN COUNTRIES MOST AT RISK OF OUTBREAKS

19-09-2025
INMAZEB ® (ATOLTIVIMAB, MAFTIVIMAB, AND ODESIVIMAB-EBGN) WAS THE FIRST TREATMENT APPROVED BY THE U...

REGENERON ANNOUNCES POSITIVE PHASE 3 TRIAL IN ADULTS WITH ULTRA-RARE GENETIC DISORDER FIBRODYSPLASIA OSSIFICANS PROGRESSIVA (FOP), DEMONSTRATING THAT GARETOSMAB PREVENTS GREATER THAN 99% OF ABNORMAL BONE FORMATION

17-09-2025
FOP IS A DISEASE IN WHICH MUSCLES, TENDONS AND LIGAMENTS ARE PROGRESSIVELY REPLACED BY BONE, LEADING...

REGENERON ALERT: BRAGAR EAGEL & SQUIRE, P.C. IS INVESTIGATING REGENERON PHARMACEUTICALS, INC. ON BEHALF OF LONG-TERM STOCKHOLDERS AND ENCOURAGES INVESTORS TO CONTACT THE FIRM

09-09-2025
NEW YORK, SEPT. 09, 2025 (GLOBE NEWSWIRE) -- BRAGAR EAGEL & SQUIRE, P.C....

REGENERON ANNOUNCES UPDATED PRESENTATION TIME FOR UPCOMING INVESTOR CONFERENCE

04-09-2025
TARRYTOWN, N.Y., SEPT. 04, 2025 (GLOBE NEWSWIRE) -- REGENERON PHARMACEUTICALS, INC. (NASDAQ: REGN)...

REGENERON ANNOUNCES POSITIVE RESULTS FROM PHASE 3 TRIAL IN GENERALIZED MYASTHENIA GRAVIS

26-08-2025
CEMDISIRAN MONOTHERAPY, DOSED SUBCUTANEOUSLY EVERY THREE MONTHS, MET THE PRIMARY AND KEY SECONDARY E...

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