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Yondelis I.V. infusion 0.25 mg/1 mg special drug use-results survey (all-case surveillance)

Yondelis I.V. infusion 0.25 mg/1 mg special drug use-results survey (all-case surveillance)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1080223101
Enrollment
140
Registered
2016-02-10
Start date
2016-02-10
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

Soft tissue sarcomas

Interventions

investigational material(s) Generic name etc : Yondelis I.V. infusion 0.25 mg/1 mg INN of investigational material : Trabectedin Therapeutic category code : 429 Other antitumor agents Dosage and Admin

Sponsors

Taiho Pharmaceutical Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients receiving Yondelis

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Safety Logistic regression

Outcome results

None listed

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