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Special drug use-results survey on ERLEADA 60 mg Tablets (Long-term use in patients with non-distant metastatic castration-resistant prostate cancer)

Special drug use-results survey on ERLEADA 60 mg Tablets (Long-term use in patients with non-distant metastatic castration-resistant prostate cancer) - ELD1L

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000036808
Enrollment
200
Registered
2019-05-31
Start date
2019-05-30
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

non-distant metastatic castration-resistant prostate cancer

Interventions

None listed

Sponsors

Janssen Pharmaceutical K.K.
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Patients with non-distant metastatic castration-resistant prostate cancer who received ERLEADA for the first time are targeted. The target patients must understand the contents of this survey and give consent to participation.

Exclusion criteria

Exclusion criteria: Patients with a history of the use of Apalutamide

Design outcomes

Primary

MeasureTime frame
[Patient composition] (a)Number of patients registered (b)Number of patients whose CRFs were collected (c)Number of patients for safety analysis (d) Number of patients excluded for analysis and the reason for exclusion [Safety analysis] (a) Incidence of safety specifications (b) Factors considered affecting safety specification (incidence by patient background, etc.)

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