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NCT02803437Completed

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

Source: ClinicalTrials.gov · Last updated 10 Jul 2025

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Observational
Enrollment
334 (actual)
First submitted
14 Jun 2016
Start date
21 Jul 2016
Primary completion date
6 Jan 2022
Lead sponsor
Bayer
NCT number
NCT02803437

What you commit to

  • Study type: Observational
  • Participants enrolled: 334
  • From 21 Jul 2016 to the primary completion date, 6 Jan 2022
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients treated Xofigo previously

Other

  • Patients participating in an investigational program with interventions outside of routine clinical practice

Who the study is looking for

  • Patients suffered from CRPC with bone metastases
  • Patients for whom the decision to initiate treatment with Xofigo is made as per physician's routine clinical practice.
  • Xofigo treatment naïve

Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
-
Coordinator of this site? Confirm its status
Multiple LocationsJapanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.