Treatment Patterns in Castrate Resistant Prostate Cancer Patients With Bone Metastases in a Medicare Population

NCT ID: NCT02518698

Last Updated: 2018-09-18

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

1163 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-08-31

Study Completion Date

2017-09-30

Brief Summary

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The goal of the study is to provide a detailed description of treatments for CRPC (Castrate Resistant Prostate Cancer) patients with bone metastases and the resource utilization and costs associated with that diagnosis and subsequent treatments.

Detailed Description

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Conditions

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Prostate Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Cohort 1 / Treatment patterns

Patients with castrated resistant prostate cancer and bone metastases

Radium-223 dichloride (Xofigo, BAY88-8223)

Intervention Type DRUG

Therapies used to treat prostate cancer and more specifically castrate resistant prostate cancer inclusively Xofigo (Radium-223 dichloride, BAY88-8223)

Interventions

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Radium-223 dichloride (Xofigo, BAY88-8223)

Therapies used to treat prostate cancer and more specifically castrate resistant prostate cancer inclusively Xofigo (Radium-223 dichloride, BAY88-8223)

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* First diagnosis for bone metastases for members diagnosed with prostate cancer found in the claims data during the identification period
* Members age ≥ 55 to 89 years at index
* Medicare members with medical and pharmacy coverage; and
* Continuously enrolled during the pre- and post-index periods.

Exclusion Criteria

* Member with diagnosis of any other cancer (excluding melanoma (ICD-9 172.x) and other metastases (ICD-9 198.x)) before the index date; and
* Members age ≥ 89 years of age at index date
Minimum Eligible Age

55 Years

Maximum Eligible Age

88 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Bayer

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Bayer Study Director

Role: STUDY_DIRECTOR

Bayer

Locations

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Louisville, Kentucky, United States

Site Status

Countries

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United States

Other Identifiers

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18273

Identifier Type: -

Identifier Source: org_study_id

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