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Special Drug Use-Results Survey for ZYTIGA Tablets 250 mg (Long-term Use)

Special Drug Use-Results Survey for ZYTIGA Tablets 250 mg (Long-term Use) - Special Drug Use-Results Survey for ZYTIGA Tablets 250 mg (Long-term Use)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000015894
Enrollment
420
Registered
2014-12-15
Start date
2014-09-16
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

castration-resistant prostate cancer

Interventions

None listed

Sponsors

Janssen Pharmaceutical K.K.
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: CRPC patients who are treated with ZYTIGA for the first time

Exclusion criteria

Exclusion criteria: NA

Design outcomes

Primary

MeasureTime frame
Safety(Adverse Drug Reaction) Effectiveness(PSA Response rate)

Secondary

MeasureTime frame
Effectiveness(Overall survival)

Countries

Japan

Contacts

Public ContactSayuri Harada

Janssen Pharmaceutical K.K. Safety Risk Management Dept.

SHarada8@its.jnj.com03-4411-5874

Outcome results

None listed

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