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All-case observational study of Gliadel(Study: GLI01S)

Post-marketing surveillance of Gliadel 7.7mg Implant (all-case observational study:GLI01S)

Status
Unknown
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1080222547
Enrollment
250
Registered
2014-06-30
Start date
2014-06-30
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

malignant glioma

Interventions

investigational material(s) Generic name etc : Gliadel 7.7mg Implant INN of investigational material : carmustine Therapeutic category code : 421 Alkylating agents Dosage and Administration for Invest

Sponsors

Eisai Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All-patient of Gliadel implantation

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
The clinical safety of 3 months after implantation Incidence Adverse events / adverse drug reactions—

Outcome results

None listed

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