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Study identifier: NCT06397703 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

ADT and SBRT vs SBRT Alone for Unfavorable Intermediate Risk Prostate Cancer

Condition: Prostate Cancer  ·  Sponsor: NYU Langone Health

PhasePhase 2
Planned participants392
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

About this study

For this study, unfavorable intermediate risk prostate cancer patients will select whether they are to be treated with the standard of care (SOC) 6 months of Androgen Deprivation Therapy (ADT) in conjunction with stereotactic body radiation therapy/radiosurgery (SBRT) directed to the prostate versus SBRT alone. The patient population will include those with National Comprehensive Cancer Network (NCCN)-defined unfavorable intermediate risk disease. All patients will be followed every 6 months for up to 5 years from the first patient treated and will undergo a routine 24-30 months post-SBRT prostate biopsy to assess for local tumor control.

This description comes directly from the study's public registry record.

Talk to the study team

Dayna Leis, RN  ·  347-266-2630  ·  Dayna.Leis@nyulangone.org

Nina Yang, RN  ·  646-830-4743  ·  Nina.Yang@nyulangone.org

Always discuss trial participation with your own doctor first.

Locations (1)

NYU Langone HealthNew York, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06397703