BLAINJECTIONINJECTABLE
Approved
Oct 2023
Lifecycle
Growth
Competitive Pressure
30/100
Clinical Trials
20
Data completeness
4/8 — Partial
Drug data last refreshed 15h ago · AI intelligence enriched 6d ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
BIMZELX (bimekizumab) is a monoclonal antibody approved in October 2023 for inflammatory dermatologic conditions including psoriasis, psoriatic arthritis, and hidradenitis suppurativa. It is administered via subcutaneous injection and represents a targeted immunologic approach to moderate-to-severe inflammatory skin and joint diseases.
$0.299MPart D
GrowthEarly-stage growth product with nascent Part D uptake (19 claims) suggests expanding commercial infrastructure and field team opportunity.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (20)
Efficacy of Bimekizumab in Adults With Pyoderma Gangrenosum
Started Sep 2026
15 enrolled
Pyoderma Gangrenosum
A Study to Learn if Bimekizumab Given in Different Ways is Safe and Moves Similarly Throughout the Body Over Time in Adults
Started Dec 2025
392 enrolled
Psoriatic ArthritisAxial Spondyloarthritis
A Study to Evaluate the Efficacy and Safety of Bimekizumab in Study Participants With Palmoplantar Pustulosis
Started Nov 2025
320 enrolled
Palmoplantar Pustulosis
A Study to Assess the Concentration of Bimekizumab in Mature Breast Milk From Mothers Receiving Treatment With Bimzelx® (Bimekizumab)
Started Nov 2025
20 enrolled
Moderate to Severe Plaque PsoriasisPsoriatic ArthritisAxial Spondyloarthritis+1 more
A Study to Assess the Pharmacokinetics and Safety of Bimekizumab in Children and Adolescents With Moderate to Severe Hidradenitis Suppurativa
Started Apr 2025
43 enrolled
Hidradenitis Suppurativa
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
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.