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Experiment to Assess Preferences for Novel Hormonal Therapy and Androgen-deprivation Therapy in Prostate Cancer Patients

Discrete Choice Experiment to Assess the Preferences for Novel Hormonal Therapy and Androgen-deprivation Therapy in Patients With Prostate Cancer

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06500741
Enrollment
374
Registered
2024-07-15
Start date
2024-11-22
Completion date
2025-04-02
Last updated
2025-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer

Keywords

Prostate Cancer, Novel hormonal therapy, Androgen-deprivation therapy

Brief summary

The purpose of this study is to quantify the preferences for novel hormonal therapy (NHT) +/- androgen-deprivation therapy (ADT) vs ADT monotherapy among patients with non-metastatic hormone-sensitive prostate cancer (PC) in the United States (US), Germany, Spain, France, Italy, the United Kingdom (UK), South Korea, Australia, and Brazil, using a discrete choice experiment (DCE).

Detailed description

The study will collect data from eligible patients (six total) and physicians (six total) from one-on-one qualitative interviews and eligible patients from online surveys. Approximately 330 patients with PC will be recruited to complete the online DCE survey.

Interventions

OTHERNo Intervention

No investigational drug will be administered to participants in this study.

Sponsors

Astellas Pharma Global Development, Inc.
Lead SponsorINDUSTRY

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Physician inclusion criteria * The physician is a certified urologist or oncologist. The final selection will be adjusted to local practice. * The physician has cared for at least ten nmHSPC patients in the past year. * The physician has experience prescribing NHT and ADT. Patient inclusion criteria * The patient has nmHSPC after radiotheraphy (RT) and/or radical prostatectomy (RP), defined as an adult patient with nmPC who had RT and/or RP.

Exclusion criteria

Physician

Design outcomes

Primary

MeasureTime frameDescription
Patients' Preference weights for different treatment attributesUp to 1 dayPreference data will be collected via online survey questionnaires designed using DCE method.
Patients' Overall Preference for a specific treatment profile (NHT +/- ADT or ADT monotherapy)Up to 1 dayPreference data will be collected via online survey questionnaires designed using DCE method.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026