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REGENERON PHARMACEUTICALS

USupdated 3mo ago
community read0 votes
pipeline
0
marketed
0
phase 3
0
catalysts ytd
0
approvals ytd
0
recalls ytd
0

Pipeline(0)

no pipeline products on record

📅 Upcoming

no upcoming catalysts on record

🕒 Recent(90d)

nothing in the last 90 days
view all catalysts →

Active trials

  • phase2Study of Olatorepatide in Adult Participants Living With Overweight or Obesity Without Diabetesrecruitingn=360
  • phase2A Study to Find Out How Safe REGN5668 is and How Well it Works In Adult Women When Given With Either Cemiplimab, or Cemiplimab + Fianlimab, or Ubamatamabrecruitingn=612
  • phase3REGN7508 in Adult Participants for Prevention of Cancer-Associated Thrombosisrecruitingn=1,120
  • phase2Safety in Adult Participants With Atrial Fibrillation Who Are Treated With Anticoagulationrecruitingn=1,200
  • phase3Treatment and Secondary Prevention of Venous Thromboembolism (VTE) in Adult Participants With Solid and Hematologic Cancersrecruitingn=1,600
  • phase2A Trial to Learn if Linvoseltamab is Safe and Works in Adults With Relapsed or Refractory Systemic Light Chain Amyloidosis (AL Amyloidosis)recruitingn=220
  • phase3A Study to Compare Linvoseltamab and Daratumumab Treatment in High-Risk Smoldering Multiple Myeloma (HR-SMM)recruitingn=270
  • phase2A Study of REGN7041 for Active Noninfectious Uveitis in Adult Participantsterminatedn=1
more trials →
🐶 Hiring Signal
No open roles indexed yet — view REGENERON PHARMACEUTICALS jobs →

News

  • Regeneron to challenge Ipsen as FDA clears bone disease drug
    Pasatru’s approval sets up a market battle in a rare indication where the only available treatment has generated disappointing sales.
    biopharma_dive · 17h ago
  • STAT+: Pharmalittle: We’re reading about a Regeneron rare disease drug, an Ultragenyx gene therapy, and more
    A Regeneron drug for an ultra-rare disease that causes bone to grow where it shouldn't won U.S. regulatory approval, capping a three-decade effort
    stat · 20h ago
  • STAT+: Regeneron drug for disease that causes dangerous bone growth earns FDA approval
    A Regeneron drug that treats an ultra-rare disease that causes bone to form where it's not meant to be has won approval.
    stat · 1d ago
  • 11 companies hiring in New Jersey
    Looking for a biopharma job in New Jersey? Job postings in the area have increased year over year, according to BioSpace data. Here are 11 companies with open roles.
    biospace · 1d ago
  • Regeneron ends eye disease study due to antibody's safety profile
    The discontinuation of the uveitis study adds to Regeneron’s series of clinical setbacks, including the Phase 3 failures of the Dupixent follow-up itepekimab and an investigational combo regimen fo…
    biospace · 2d ago
  • Regeneron ends eye disease study due to antibody's safety profile
    The discontinuation of the uveitis study adds to Regeneron’s series of clinical setbacks, including the Phase 3 failures of the Dupixent follow-up itepekimab and an investigational combo regimen fo…
    biospace · 2d ago
  • EyePoint plummets on pivotal data for main drug
    Though its drug missed the key goal of a wet AMD study, EyePoint — as well as analysts — see a path toward approval. Investors may be harder to win over, however.
    biopharma_dive · 3d ago
  • EyePoint’s Phase 3 fail sends stock spiraling amid next-gen AMD race
    EyePoint’s quest to reduce treatment burden for patients with age-related macular degeneration has hit a bump in the road, with a clinical miss driving the biotech’s stock down by 70%.
    biospace · 3d ago
  • Regeneron ends eye disease trial for anti-CD3 antibody following safety review
    Regeneron has hit the brakes on the phase 1/2a trial for an experimental eye inflammation treatment, following an adverse event that tilted the drug’s risk/benefit profile in the wrong direction.
    fiercebiotech · 3d ago
  • 7 companies hiring in North Carolina now
    Looking for a biopharma job in North Carolina? Job postings in the area have increased. Here are seven companies with open roles.
    biospace · 8d ago
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