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  1. pharmadog
  2. ›drugs
  3. ›DUPIXENT
drug · antibody
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DUPIXENT

updated 5mo ago
/ dew-PIL-oo-mab /
by $REGN REGENERON PHARMACEUTICALS, INC.🔗 ChEMBL
community read0 votes

🐶 often sniffed alongside

top 7
  • drugdupilumab126 co-mentions · 33 sources
  • tagApproval124 co-mentions · 31 sources
  • tagPulmonology1 co-mentions · 1 sources
  • tagAsthma1 co-mentions · 1 sources
  • tagPDUFA1 co-mentions · 1 sources
  • tagDermatology1 co-mentions · 1 sources
  • companyBrigham and Women's Hospital1 co-mentions · 1 sources

Antibody drug with a maximum clinical stage of Approval (across all indications), with 8 approved and 30 investigational indications.

targets

Interleukin-4 receptor subunit alpha

all catalysts(0)

nothing on the calendar yet

Trials studying DUPIXENT

  • phase3A Study Assessing the Effect of Dupilumab on Inducing Clinical Remission in Asthmarecruitingn=150
  • —Real-World Effectiveness of Dupilumab in Patients With Prurigo Nodularis: An Observational Studycompletedn=110
  • phase3A Study of Dupilumab in Small Children With an Allergic Condition of the Esophagus (Food Pipe): Eosinophilic Esophagitisrecruitingn=20
  • phase4A Study to Investigate Airway Inflammation With Dupilumab Subcutaneously in Participants Aged ≥40 to ≤85 Years With Chronic Obstructive Pulmonary Disease.recruitingn=218
  • phase2Study to Assess Efficacy and Safety of Dupilumab in the Treatment of Keloidscompletedn=20
  • —A Non-interventional Observational Study to Assess Long-term Efficacy and Safety of Dupilumab for the Treatment of Patients (>= 12 Years) With Eosinophilic Esophagitis Under Real-world-conditions in Germanyrecruitingn=150
  • phase3Dupilumab in Allergic Fungal Rhinosinusitis (AFRS)completedn=62
  • —A Study to Observe How Pediatric Patients With Severe Atopic Dermatitis Despite Less Extensive Skin Lesions Respond to Dupilumab Treatmentrecruitingn=230

News(10)

  • Lilly, Foghorn part ways; Wave’s FDA-approved plans
    The pharma giant cut its partnership after a cancer drug disappointed in testing. Elsewhere, Teva and Samsung Bioepis expanded a partnership and space biotech Varda brought in $251 million.
    biopharma_dive · 2d ago
  • Sanofi, Regeneron broaden alliance to find their next Dupixent
    The deal carries a $1 billion upfront payment and tasks the two companies to develop long-acting antibody drugs that go after the same targets as their blockbuster anti-inflammation agent.
    biopharma_dive · 2d ago
  • Pfizer’s eczema drug clears skin in mid-stage trial
    Detailed results are competitive with Dupixent and Ebglyss, but the drug lacks differentiation amid an increasingly competitive landscape, one analyst argued.
    biopharma_dive · 2d ago
  • Sanofi pays Regeneron $1B upfront to continue search for Dupixent successor
    Sanofi and Regeneron have had a long and “sometimes contentious” partnership, BMO Capital Markets noted, as the companies contend with the looming loss of exclusivity of their blockbuster drug Dupi…
    biospace · 2d ago
  • Sanofi builds on immunology alliance with Regeneron for $1B upfront
    As the patent cliff for Dupixent draws closer, Sanofi is turning back to the partnership that built the megablockbuster. The French pharma will pay $1 billion upfront to expand its antibody collabo…
    endpoints · 3d ago
  • STAT+: Sanofi, Regeneron expand partnership after Dupixent success
    Sanofi and Regeneron have re-upped their collaboration pact, aiming to build on the blockbuster success of the drug Dupixent.
    stat · 3d ago
  • Sanofi pays Dupixent partner Regeneron $1B upfront for 4 early-stage assets to ignite R&D
    Sanofi is paying Regeneron $1 billion upfront to collaborate on four early-stage immunology programs, teeing the longstanding partners up to try to replicate Dupixent’s success.
    fiercebiotech · 3d ago
  • Recon: Sanofi, Regeneron expand partnership after Dupixent success; Lilly amylin-Zepbound combo succeeds in mid-stage trial
    Welcome to Regulatory Reconnaissance, your regulatory news and intelligence briefing.
    raps · 3d ago
  • Connect’s Dupixent rival reduces COPD attacks by 85%, but misses a secondary goal
    Connect Biopharma has pointed to phase 2 data for its IL-4/IL-13 blocker as proof that the wannabe Dupixent rival can reduce respiratory attacks—although the study missed a secondary endpoint tied…
    fiercebiotech · 4d ago
  • 6 immunology targets to sustain a mammoth I&I market
    Johnson & Johnson, Pfizer, Argenx and more are unlocking new immunology targets and looking to improve on existing ones in an attempt to catch some of the magic brought about by AbbVie’s Humira and…
    biospace · 6d ago
view all news mentions →
brand
DUPIXENT
trade names
Dupixent, Regn668, sar231893
generic
DUPILUMAB
MOA
12.1 Mechanism of Action Dupilumab is a human monoclonal IgG4 antibody that inhibits interleukin-4 (IL-4) and interleukin-13 (IL-13) signaling by specifically binding to the IL-4Rα subunit shared by the IL-4 and IL-13 receptor complexes. Dupilumab inhibits IL-4 signaling via the Type I receptor and both IL-4 and IL-13 signaling through the Type II receptor. Inflammation driven by IL-4 and IL-13 is an important component in the pathogenesis of asthma, AD, CRSwNP, EoE, PN, COPD, CSU, BP, and AFRS. Multiple cell types that express IL-4Rα (e.g., mast cells, basophils, eosinophils, macrophages, lymphocytes, epithelial cells, goblet cells) and inflammatory mediators (e.g., histamine, eicosanoids, leukotrienes, cytokines, chemokines) are involved in inflammation. Blocking IL-4Rα with dupilumab inhibits IL-4 and IL-13 cytokine-induced inflammatory responses, including the release of proinflammatory cytokines, chemokines, nitric oxide, and IgE. The mechanism of dupilumab action has not been definitively established.
indication
1 INDICATIONS AND USAGE DUPIXENT is an interleukin-4 receptor alpha antagonist indicated: Atopic Dermatitis for the treatment of adult and pediatric patients aged 6 months and older with moderate-to-severe AD whose disease is not adequately controlled with topical prescription therapies or when those therapies are not advisable. DUPIXENT can be used with or without topical corticosteroids. ( 1.1 ) Asthma as an add-on maintenance treatment of adult and pediatric patients aged 6 years and older with moderate-to-severe asthma characterized by an eosinophilic phenotype or with oral corticosteroid dependent asthma. ( 1.2 ) Limitations of Use: Not for the relief of acute bronchospasm or status asthmaticus. ( 1.2 ) Chronic Rhinosinusitis with Nasal Polyps as an add-on maintenance treatment in adult and pediatric patients aged 12 years and older with inadequately controlled chronic rhinosinusitis with nasal polyps (CRSwNP). ( 1.3 ) Eosinophilic Esophagitis for the treatment of adult and pediatric patients aged 1 year and older, weighing at least 15 kg, with eosinophilic esophagitis (EoE). ( 1.4 ) Prurigo Nodularis for the treatment of adult patients with prurigo nodularis (PN). ( 1.5 ) Chronic Obstructive Pulmonary Disease as an add-on maintenance treatment of adult patients with inadequately controlled chronic obstructive pulmonary disease (COPD) and an eosinophilic phenotype. ( 1.6 ) Limitations of Use: Not for the relief of acute bronchospasm. ( 1.6 ) Chronic Spontaneous Urticaria for the treatment of adult and pediatric patients aged 12 years and older with chronic spontaneous urticaria (CSU) who remain symptomatic despite H1 antihistamine treatment. ( 1.7 ) Limitations of Use: Not indicated for other forms of urticaria. ( 1.7 ) Bullous Pemphigoid for the treatment of adult patients with bullous pemphigoid (BP). ( 1.8 ) Allergic Fungal Rhinosinusitis for the treatment of adult and pediatric patients aged 6 years and older with allergic fungal rhinosinusitis (AFRS) who h
Data sources
ClinicalTrials.gov · OpenTargets
last refreshed 4h ago
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