LITHOSTAT (acetohydroxamic acid) by Mission Therapeutics is urease inhibitors [moa]. First approved in 1983.
Drug data last refreshed 9h ago · AI intelligence enriched 3w ago
LITHOSTAT (acetohydroxamic acid) is an oral urease inhibitor approved in 1983 for the management of struvite kidney stones by reducing urease-producing bacterial activity. It works by inhibiting the enzyme urease, which prevents the formation of alkaline urine that promotes stone crystal formation. This niche mechanism addresses a specific urological condition with limited therapeutic alternatives.
Declining commercial interest with minimal Part D spend ($572K in 2023) signals a small, legacy franchise with limited team expansion opportunities.
Urease Inhibitors
Urease Inhibitor
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
LITHOSTAT represents a late-stage, niche product career opportunity with minimal growth trajectory and limited visibility; roles focus on maintenance of a small installed base rather than expansion or innovation. Career development on this legacy product is constrained by flat commercial metrics, zero linked job openings, and absence of clinical pipeline activity.
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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.
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