NDATOPICALSOLUTIONPriority Review
Approved
Dec 1990
Lifecycle
LOE Approaching
Competitive Pressure
30/100
Data completeness
4/8 — Partial
Priority Review
CONDYLOX (podofilox) by Teva is mechanism of action treatment of anogenital warts with podofilox results in necrosis of visible wart tissue. Approved for the treatment of mucous membrane warts (see ). First approved in 1990.
Drug data last refreshed 20h ago · AI intelligence enriched 2w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
CONDYLOX (podofilox) is a topical solution indicated for treatment of anogenital warts (mucous membrane warts) approved in 1990. The drug works by inducing necrosis of visible wart tissue, though the exact molecular mechanism remains unknown. It is a small molecule therapeutic applied directly to affected tissue.
$0.017BPart D
LOE ApproachingLOE-approaching product with minimal Part D spending ($17K) indicates small, stable team focused on managed decline and generic transition support.
Mechanism of Action
Mechanism of Action Treatment of anogenital warts with podofilox results in necrosis of visible wart tissue. The exact mechanism of action is unknown.
Indications (1)
Career Relevance
CONDYLOX represents a mature, low-activity asset with zero linked job openings, indicating minimal hiring and career mobility. Working on this product offers limited growth potential but stable compliance and customer service responsibilities in a declining market.
Brand Manager (Legacy Management)
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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.