NDATOPICALCREAM
Approved
Nov 2013
Lifecycle
Peak
Competitive Pressure
0/100
Clinical Trials
3
Data completeness
7/8 — Comprehensive
LUZU (luliconazole) by Bausch + Lomb is cytochrome p450 2c19 inhibitors [moa]. Approved for azole antifungal [epc]. First approved in 2013.
Drug data last refreshed 14h ago · AI intelligence enriched 1mo ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
LUZU (luliconazole) is a topical azole antifungal cream approved in 2013 for dermatological fungal infections. It works by inhibiting fungal cytochrome P450 2C19, disrupting ergosterol synthesis and fungal cell membrane integrity. The product is currently in peak lifecycle stage with stable market presence.
$0.018MPart D
PeakStable
7.5 years to LOELUZU maintains stable peak-stage revenue with minimal Part D claims, indicating a niche market position that may support focused but smaller commercial teams compared to blockbuster competitors.
Mechanism of Action
Cytochrome P450 2C19 Inhibitors
Pharmacologic Class:
Azole Antifungal
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (3)
Safety and Efficacy of Product 33525 (Luliconazole Cream 1%) in Pediatric Participants With Tinea Corporis
Started Feb 2016
75 enrolled
Tinea Corporis
Maximal Use of Luliconazole Cream 1% in Pediatric Participants With Moderate to Severe Tinea Pedis or Tinea Cruris
Started Dec 2015
30 enrolled
Tinea PedisTinea Cruris
Study Evaluating the Drug Interaction Potential of Luliconazole Cream 1% in Participants With Tinea Pedis and Tinea Cruris
Started Feb 2015
20 enrolled
Tinea PedisTinea Cruris
Career Relevance
LUZU offers career opportunities primarily in commercial and medical affairs focused on dermatological market penetration and managed care engagement. The stable peak-stage lifecycle suggests predictable but modest team growth, with emphasis on competitive differentiation against JUBLIA and systemic alternatives rather than innovation or expansion.
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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.