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Post-marketing clinical study of Topina tablets

Post-marketing clinical study of Topina tablets in patients with partial epilepsy (incremental dose comparative study)

Status
Unknown
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1080220856
Enrollment
180
Registered
2009-09-09
Start date
2009-09-09
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Partial epilepsy

Interventions

investigational material(s) Generic name etc : Topina tablets (INN:topiramate) INN of investigational material : Therapeutic category code : 113 Antiepileptics Dosage and Administration for Investiga

Sponsors

Kyowa Hakko Kirin Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who continue the treatment of one or more antiepileptic drugs with same usage and dosage except Topina tablets Patients who experience one or more partial seizures in every four weeks regardless of the treatment of antiepileptic drugs except Topina tablets

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Safety

Secondary

MeasureTime frame
Efficacy

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026