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AMGEN

USupdated 4mo ago
community read0 votes
pipeline
1
marketed
0
phase 3
0
catalysts ytd
0
approvals ytd
0
recalls ytd
0

Pipeline(1)

pipeline depth1 products
Unknown: 1
1Unknown
drug
PROCRIT

📅 Upcoming

no upcoming catalysts on record

🕒 Recent(90d)

nothing in the last 90 days
view all catalysts →

Active trials

  • phase3A Phase 3 Study of Inebilizumab in Participants With Primary Membranous Nephropathyrecruitingn=159
  • phase4A Study to Evaluate Avacopan in Participants With ANCA-associated Vasculitisrecruitingn=300
  • phase3A Study to Evaluate Efficacy, Safety, and Immunogenicity With ABP 938 8 mg Versus EYLEA® HD (Aflibercept) in Participants With Neovascular Age-related Macular Degenerationrecruitingn=304
  • phase1Evaluation of Xaluritamig in Adults, Adolescents and Children With Relapsed or Refractory Ewing Sarcoma (EWS)recruitingn=50
  • phase3A Study of Xaluritamig Plus Abiraterone Versus Investigator's Choice in Participants With Chemotherapy-naïve Metastatic Castration-resistant Prostate Cancerrecruitingn=750
  • phase3Efficacy and Safety of Erenumab in Pediatric Participants With Episodic Migraineactive not recruitingn=457
  • phase4A Trial to Investigate the Non-inferiority of Pegloticase Administered Every 4 Weeks (Q4W) With MTX Compared With Every 2 Weeks (Q2W) With MTX in Participants With Uncontrolled Refractory Goutcompletedn=306
  • phase3A Study Evaluating Subcutaneous Versus Intravenous Blinatumomab in Newly Diagnosed Adults With B-cell Precursor Acute Lymphoblastic Leukaemianot yet recruitingn=560
🐶 Hiring Signal
No open roles indexed yet — view AMGEN jobs →

News

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  • Novartis bets up to $7.8B for an mRNA-encoded T cell engager from China’s Abogen
    Novartis is licensing an mRNA-based therapy designed to produce a CD3xCD19 T cell engager inside the body. Abogen Biosciences says the in vivo approach could reduce the likelihood of dangerous cyto…
    biospace · 2d ago
  • Novartis pens $7.8B deal for Abogen's in vivo autoimmune T-cell engager
    Novartis is paying Abogen Biosciences $575 million upfront for an mRNA-encoded T-cell engager that showed early clinical promise in autoimmune disease. The deal, which includes up to $7.2 billion i…
    fiercebiotech · 3d ago
  • Chutes & Ladders—Bayer taps new chief medical officer; Cantor appointed PhRMA CEO
    Eric Cantor, who represented Virginia in the U.S. House of Representatives for 14 years and served as House majority leader from 2011 to 2014, will step up as PhRMA’s next president and CEO on Nov.…
    fiercebiotech · 3d ago
  • Patient death in BMS pulmonary fibrosis trial raises questions, but analysts unshaken
    The revelation of a patient death in Bristol Myers Squibb’s phase 3 trial of a potential pulmonary fibrosis treatment has raised concerns ahead of the study’s readout, but analysts were quick to di…
    fiercebiotech · 3d ago
  • The top 12 companies hiring in biopharma now
    Looking for a biopharma job? Check out the BioSpace list of 12 top companies hiring life sciences professionals like you.
    biospace · 4d ago
  • Bristol Myers trial revisions shake confidence in new class of fibrosis drugs
    A spokesperson confirmed that a “limited number” of liver-related safety events, including a patient death, were observed in testing of Bristol Myers’ admilparant — though it’s unclear whether the…
    biopharma_dive · 4d ago
  • Amgen reveals 6-point drop in lupus severity behind phase 2 win for Horizon antibody
    Amgen has shed light on its phase 2 lupus win, revealing that its monoclonal antibody daxdilimab was tied to a 6-point reduction in disease severity at the lower dose.
    fiercebiotech · 5d ago
  • Merck, Daiichi end plans to seek speedy approval of lung cancer ADC
    The FDA indicated that the data generated so far wouldn’t support an accelerated clearance of “I-DXd,” a setback that erases an edge Merck and Daiichi had over multiple fast-moving competitors.
    biopharma_dive · 6d ago
  • Merck, Daiichi pull lung cancer filing after FDA pushback deals another blow to $4B deal
    Daiichi Sankyo and Merck & Co. have withdrawn an antibody-drug conjugate (ADC) filing after the FDA said they lacked the data for accelerated approval in a lung cancer population.
    fiercebiotech · 7d ago
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