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NCT02066961: ASPIRE-PCa

A Study to Describe Patterns of Care and Outcomes of Men Who Are at High Risk After Experiencing Biochemical Failure Following Definitive Prostate Cancer Therapy, Men With Castration-resistant Prostate Cancer and Men With Metastatic Prostate Cancer

Completed Last updated 20 December 2019
What this trial tests

trial in Prostate Cancer in 1,533 participants. Completed in 14 November 2019.

Timeline
31 December 2013
Primary endpoint
14 November 2019
14 November 2019

Quick facts

Lead sponsorAstellas Pharma Global Development, Inc.
StatusCompleted
Study typeOBSERVATIONAL
Enrollment1,533
Start date31 December 2013
Primary completion14 November 2019
Estimated completion14 November 2019
Sites93 locations across Italy, Colombia, Taiwan, South Korea, Philippines, Lebanon, New Zealand, Netherlands

Conditions studied

Sponsor

Astellas Pharma Global Development, Inc. — full company profile →

Who can join

Eligibility, male only, with Prostate Cancer or Castration-resistant Prostate Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to describe patterns in disease management and to describe clinical outcomes, as well as to identify factors influencing physician treatment decisions including reason(s) for treatment choices and trigger(s) for treatment changes and to document healthcare resource utilization used to manage treatment-related complications.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Prostate Cancer

Currently open trials in the same condition.

Other Astellas Pharma Global Development, Inc. trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02066961.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing