Clinical Trials Directory

Trials / Completed

CompletedNCT02803437

Drug Use Investigation of Xofigo, Castration Resistant Prostate Cancer With Bone Metastases

Status
Completed
Phase
Study type
Observational
Enrollment
334 (actual)
Sponsor
Bayer · Industry
Sex
Male
Age
Healthy volunteers
Not accepted

Summary

This study is a Japanese post-marketing surveillance (PMS) which is required by the regulatory authorities. General objective of PMS is to confirm the clinical usefulness, especially the safety profile of a drug under the routine clinical practice.

Detailed description

This is a local, non-interventional, multi-center, single-cohort study using primary data of patients treated with Xofigo for the indication of castration resistant prostate cancer (CRPC) with bone metastases. A total of 300 patients (valid for safety analysis) are enrolled within 18 months. During the observation period (i.e. up to 6 months), safety and effectiveness information is collected. Since patient's visit occurs under the routine clinical practice, the study protocol does not define exact referral dates for those visits. The physician records patient data as defined in the protocol. The extended follow-up period is to collect bone fractures and survival with post-treatment information after Xofigo under the real-world in Japan. The results of this study (except of extended follow-up period) have to be submitted to the Japanese regulatory authorities as a part of the reexamination period (8 years). This study is conducted in accordance with Article 14-4 (re-examination) of the Pharmaceutical Affairs Law, and Good Post-marketing Surveillance Practice from a ministerial ordinance of Ministry of Health, Labor and Welfare in Japan.

Conditions

Interventions

TypeNameDescription
DRUGRadium-223 dichloride (Xofigo, BAY 88-8223)Xofigo treatment will be performed according to the product label in Japan under the routine clinical practice.

Timeline

Start date
2016-07-21
Primary completion
2022-01-06
Completion
2024-12-18
First posted
2016-06-17
Last updated
2025-07-10

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT02803437. Inclusion in this directory is not an endorsement.