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Trials / Active Not Recruiting

Active Not RecruitingNCT05901649

A Study for the Participants With Metastatic Hormone Sensitive Prostate Cancer (mHSPC) Treated With Androgen Deprivation Therapy (ADT) Plus Apalutamide or Enzalutamide

Prospective, Multi-Country, Observational Study of Clinical Outcomes for Participants With Metastatic Hormone Sensitive Prostate Cancer (mHSPC) Treated With ADT Plus Apalutamide or Enzalutamide Under Routine Clinical Practice (ArtemisPRO)

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
504 (actual)
Sponsor
Janssen-Cilag Ltd. · Industry
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess the real-world outcomes differences between apalutamide or enzalutamide plus androgen deprivation therapy (ADT) for the treatment of participants with metastatic hormone-sensitive prostate cancer (mHSPC).

Conditions

Interventions

TypeNameDescription
DRUGApalutamideNo interventions will be administered as a part of this study. Participants will receive apalutamide as per their routine clinical practice.
DRUGEnzalutamideNo interventions will be administered as a part of this study. Participants will receive enzalutamide as per their routine clinical practice.

Timeline

Start date
2023-07-05
Primary completion
2026-06-05
Completion
2026-06-05
First posted
2023-06-13
Last updated
2026-04-13

Locations

53 sites across 6 countries: Austria, France, Germany, Greece, Spain, United Kingdom

Source: ClinicalTrials.gov record NCT05901649. Inclusion in this directory is not an endorsement.