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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04516161
Other study ID # 20977
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 3, 2020
Est. completion date March 31, 2021

Study information

Verified date March 2022
Source Bayer
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In this observational study researchers want to gather more information about the characteristics of patients treated with Radium-223 (Xofigo) who had survived over a long period of time prostate cancer that had spread to other places in the body and keeps growing even when the amount of testosterone in the body is reduced to very low levels (metastatic castration-resistant prostate cancer, mCRPC). In addition researchers want to identify the factors which may contribute to survival over a long period of time in those patients. Radium-223 (Ra-223) is an alpha particle-emitting radioactive agent approved for the treatment of men with metastatic castration-resistant prostate cancer (mCRPC).


Recruitment information / eligibility

Status Completed
Enrollment 1180
Est. completion date March 31, 2021
Est. primary completion date March 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria - Adult patients with documented diagnosis of mCRPC (=18 years at diagnosis), and - Received Ra-223 as one of the therapies between Jan 1, 2013 and Jun 31, 2019 after diagnosis of mCRPC Exclusion criteria - Patients involved in clinical trials

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Radium-223 dichloride (Xofigo, BAY88-8223)
Receiving Ra-223 either alone or in combination with other cancer therapies at any time after diagnosis of mCRPC

Locations

Country Name City State
United States Bayer Flatiron Xofigo Registry database Whippany New Jersey

Sponsors (1)

Lead Sponsor Collaborator
Bayer

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Overall survival from initiation of Ra-223 Retrospective analysis from Jan 2013 to Dec 2019
Secondary Percentage of Prostate Specific Antigen (PSA) (unit: µg/L) response after Ra-223 PSA response will be defined = 50% reduction in baseline PSA level after initiation of Ra-223 Retrospective analysis from Jan 2013 to Dec 2019
See also
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Active, not recruiting NCT03724747 - Study to Evaluate the Safety, Tolerability,Pharmacokinetics, and Antitumor Activity of a Thorium-227 Labeled Antibody-chelator Conjugate Alone and in Combination With Darolutamide, in Patients With Metastatic Castration Resistant Prostate Cancer Phase 1
Withdrawn NCT02130947 - Exercise Intervention for Pts With Metastatic Castration-Resistant Prostate Cancer Receiving Abiraterone or Enzalutamide N/A