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Special Drug Use-results Survey for long-term use of Doxil injection 20mg (ovarian cancer aggravated after chemotherapy)

Special Drug Use-results Survey for long-term use of Doxil injection 20mg (ovarian cancer aggravated after chemotherapy) - Special Drug Use-results Survey for long-term use of Doxil injection 20mg (ovarian cancer aggravated after chemotherapy)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000015902
Enrollment
500
Registered
2014-12-15
Start date
2009-04-22
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

ovarian cancer aggravated after chemotherapy

Interventions

None listed

Sponsors

Janssen Pharmaceutical K.K.
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: All patients who were treated with Doxil injection 20mg

Exclusion criteria

Exclusion criteria: NA

Design outcomes

Primary

MeasureTime frame
Safety(Adverse Drug Reaction) Effectiveness(Antitumor efficacy)

Countries

Japan

Contacts

Public ContactTomohiko Shigemasa

Janssen Pharmaceutical K.K. Safety Risk Management Dept.

tshigema@its.jnj.com03-4411-5874

Outcome results

None listed

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