DIACOMIT (stiripentol) by Biocodex is unknown. Approved for dravet syndrome. First approved in 2018.
Drug data last refreshed 22h ago · AI intelligence enriched 2w ago
DIACOMIT (stiripentol) is an oral suspension anticonvulsant approved in 2018 for rare pediatric epilepsies, particularly Dravet syndrome and pharmacoresistant focal epilepsies. Its mechanism of action remains incompletely understood but likely involves GABA-A receptor modulation and cytochrome P450 inhibition, which increases blood levels of concomitant antiepileptic drugs like clobazam. The drug addresses a critical unmet need in severe, treatment-resistant pediatric epilepsy.
DIACOMIT is in peak lifecycle phase but generates minimal commercial revenue ($1M Part D spending), indicating a niche market with limited team expansion potential.
unknown. Possible mechanisms of action include direct effects mediated through the gamma-aminobutyric acid (GABA) A receptor and indirect effects involving inhibition of cytochrome P450 activity with resulting increase in blood levels of clobazam and its active metabolite.
Bioavailability of Stiripentol After Single Oral Dose of Capsule vs Suspension in Healthy Subjects (STILIQ)
Evaluation of the Efficacy and Safety of Stiripentol in Patients 6 Years and Older With Primary Hyperoxaluria Type 1, 2 or 3
Pharmacokinetic Parameters of Stiripentol in Renal Impaired Patients and Matching Controls With Normal Renal Function
Study of Interest of Stiripentol and Carbamazepine in the Treatment of Patients With Pharmacoresistant Focal Epilepsies
Retrospective Non-interventional Study of Stiripentol Use in Dravet Patients in the USA
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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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Upgrade to Pro — $25/moDIACOMIT is a niche pediatric epilepsy product with minimal commercial traction ($1M annual spending) and approaching patent expiration (3.2 years), creating very limited career opportunities. Roles on this product would focus on defending market share in a declining revenue scenario rather than growth or innovation.