No US antiseizure indication. In the UK, Ospolot 20 mg/mL oral suspension is indicated for Rolandic epilepsy (benign childhood epilepsy with centrotemporal spikes), now termed self-limited epilepsy with centrotemporal spikes (SeLECTS). The UK label is not U.S. approval.
Role
Maintenance · UK-labeled SeLECTS use
Class
Carbonic anhydrase inhibitor — sulfonamide
UK SmPC and patient-leaflet PDF checked 26 September 2026. The cited UK product is Ospolot 20 mg/mL oral suspension. Its indication and weight criteria do not establish U.S. approval or apply automatically to other formulations.
Ospolot 20 mg/mL oral suspension · UKUK label Self-limited epilepsy with centrotemporal spikes (SeLECTS) · Children and adolescents weighing at least 12 kg; no numerical minimum age specified · Maintenance
UK label for Rolandic epilepsy / SeLECTS. Requires an experienced pediatric neurologist; weight must be at least 12 kg. The label notes limited controlled-trial evidence. No US antiseizure indication.
The cited UK indication and dosing guidance concern pediatric Rolandic epilepsy / SeLECTS; no adult regimen is summarized.
Pediatric
UK SmPC: maintenance approximately 5–10 mg/kg/day, usually divided into three doses, for children and adolescents weighing at least 12 kg.
Titration / repeat dosing
UK SmPC: titrate individually over about one week; its starting-dose examples use 2.5 mg/kg/day. An experienced pediatric neurologist determines treatment duration and withdrawal; do not stop abruptly.
Dose basis
UK Ospolot oral-suspension SmPC; international labeling, not a U.S. indication.
Practical administration
Product instructions
UK oral suspension: 20 mg/mL. Shake well for at least 30 seconds, then draw up the dose immediately with the supplied oral syringe. See the product instructions for administration and feeding-tube use.
Caution: substantial urinary elimination; no validated renal dose table in the cited UK label. Closely monitor renal function and interacting phenytoin.
Hepatic impairment
Monitor liver enzymes; no validated hepatic dose algorithm in the cited UK label.
Serum reference information
No validated routine therapeutic range in the cited label. Use clinical response; monitor affected partner-drug levels when indicated.
Safety
Boxed warning
No U.S. boxed warning because no U.S. approved label was identified. International serious precautions still apply.
Contraindications
UK SmPC: hypersensitivity to sulthiame, other sulfonamides or excipients; hyperthyroidism; arterial hypertension; acute porphyria.
Serious precautions & monitoring
Monitor for metabolic acidosis, hyperventilation, paresthesias, renal stones, severe skin reactions and blood/liver/renal toxicity. The UK SmPC recommends CBC, liver enzymes and renal function before treatment, weekly for the first month, monthly for the first 6 months, then 2–4 times yearly. Stop for a persistent creatinine increase; severe hypersensitivity or symptomatic progressive thrombocytopenia/leukopenia also requires discontinuation. Exercise particular caution in renal impairment, psychiatric disease and Leber hereditary optic neuropathy.
Human sulthiame pregnancy data are limited; animal embryotoxicity is reported. The UK SmPC does not recommend use during pregnancy.
Contraception
The UK SmPC also does not recommend sulthiame in people who could become pregnant and are not using contraception.
Pregnancy / postpartum monitoring
If treatment is necessary during pregnancy, the UK SmPC recommends the lowest seizure-controlling dose, preferably as monotherapy, and prenatal assessment for malformations.
Research summaries describe studied populations and outcomes; they do not add indications or constitute treatment recommendations.
Randomized controlled trialGuideline-supported off-label use
Trial summary
Primary endpoint
Six-month randomized placebo-controlled SeLECTS study (66 children, ages 3–11): treatment failure included a seizure after the 7-day run-in, intolerable adverse events, another epilepsy syndrome, or withdrawal requested by the family.
Results
No treatment-failure event: 25/31 (81%) with sulthiame versus 10/35 (29%) with placebo. This composite is not a pure seizure-freedom rate; this was not a U.S. registration trial.
Confidence intervals
A confidence interval is not reported in the PubMed abstract.
Discontinuations
No participant withdrew for adverse events in the published abstract; two placebo families requested withdrawal and four participants stopped for administrative reasons.
Exposure duration
Six months; sulthiame 5 mg/kg/day versus placebo in the published trial.
Seizure-frequency results
The UK SmPC states that controlled-trial evidence is limited and does not report a registration-style median seizure-frequency reduction.
Responder rate
No 50% responder rate is reported in the cited UK SmPC.
Seizure freedom
No seizure-freedom rate is reported in the cited UK SmPC; SeLECTS also has a high spontaneous-remission rate, so uncontrolled outcomes require caution.
NICE places sulthiame after unsuccessful trials of lamotrigine and levetiracetam; this sequence is guideline positioning, not head-to-head evidence of superiority. The UK SmPC notes limited controlled-trial evidence and a high spontaneous-remission rate in SeLECTS.
Mechanism of action
Inhibits carbonic anhydrase; altered acid–base regulation is associated with reduced neuronal excitability. The complete clinical antiseizure mechanism is not established.
This is not a benzodiazepine or a direct GABA-A receptor modulator. Carbonic-anhydrase effects also explain acidosis and kidney-stone concerns.
Adult values unless specified. Vd/F denotes apparent oral distribution volume.
Pharmacokinetics
Bioavailability
Rapid oral absorption; a reliable absolute bioavailability value is not provided in the UK SmPC or the cited human pilot study.
Elimination half-life
Approximately 12 hours after a single dose in healthy adults (UK SmPC); shorter values may occur in children. The small pilot study found nonlinear plasma/erythrocyte disposition.
Volume of distribution
Pilot adult model: apparent plasma compartment approximately 64.8 L, plus a saturable erythrocyte compartment of 3.3 L. These are model estimates from four volunteers, not validated pediatric dosing constants.
Active metabolite(s)
No clinically established active metabolite contribution reported in the cited sources.
Active-metabolite half-life
Not established in the cited human/product sources.
Protein binding
Approximately 29% in the UK SmPC.
Metabolism / elimination
Approximately 32% excreted unchanged in urine within 24 hours; urinary and fecal elimination contribute.
International drug: pharmacokinetic evidence remains limited; do not assume linear kinetics or equate plasma and whole-blood concentrations.
Country-dependent; no U.S. approved generic identified.
Related drugs
See mechanism and syndrome guidance.
Sources & review status
UK SmPC and patient-leaflet PDF checked: 2026-09-26. Other profile sources reviewed: 2026-09-15 · label revision noted at that review: See linked product label. This is a draft reference; final review is pending.