Drug data last refreshed 16h ago · AI intelligence enriched 1w ago
EXDENSUR (depemokimab) is a monoclonal antibody (mAb) approved by the FDA in December 2025 as a subcutaneous injection. The specific indication and mechanism of action are not yet disclosed in available data. Patient population and therapeutic application require clinical trial data review.
Early-stage launch product with moderate competitive pressure (30/100) suggests a focused commercial team building market presence in a moderately crowded space.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Efficacy and Safety of Depemokimab Monotherapy Without Concomitant Use of Intranasal Corticosteroids (INCS) in Japanese Participants With Chronic Rhinosinusitis With Nasal Polyps (CRSwNP)
A Study of Depemokimab in Participants of 6 to 11 Years of Age
A Study of Efficacy and Safety of Depemokimab Compared With Placebo in Adults and Adolescents With at Risk Type 2 Asthma
eValuating the Efficacy and Safety of InitiatinG depemokImab earLy therApy iN Chronic Obstructive Pulmonary Disorder (COPD) With Type 2 Inflammation
Depemokimab as an Extended treatmeNt Duration Biologic in Adults With Chronic Obstructive Pulmonary Disease (COPD) and Type 2 Inflammation (ENDURA-2)
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
EXDENSUR represents a launch-stage mAb opportunity with GSK, ideal for professionals seeking early-stage commercial exposure in a moderately competitive market. Roles focus on market penetration, payer engagement, and field execution during critical first-year establishment.