Patient Guide: Androgen Suppression Combined With Nodal Irradiation and Dose Escalated Prostate Treatment

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 13 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06235697
Status: 🟢 Enrolling Now
Condition: Prostate Cancer
Phase: PHASE3

Where You Can Participate

This study is available at 13 locations across the country.

Top locations include:
  • • City of Saint Peters, Missouri
  • • Creve Coeur, Missouri
  • • St Louis, Missouri
  • • And 10 more locations

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Androgen Suppression Combined With Nodal Irradiation and Dose Escalated Prostate Treatment - Join Clinical Trial NCTNCT06235697

How to Join This Clinical Trial - NCTNCT06235697

Learn how to participate in this PHASE3 trial studying an investigational therapy for Prostate Cancer. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Prostate Cancer. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Prostate Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06235697 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 13 locations. Find a study site near you:

Clinical Research Site

City of Saint Peters, Missouri 63376 - United States

Status: RECRUITING

Clinical Research Site

Creve Coeur, Missouri 63141 - United States

Status: RECRUITING

Clinical Research Site

St Louis, Missouri 63110 - United States

Status: RECRUITING

Clinical Research Site

St Louis, Missouri 63129 - United States

Status: RECRUITING

Clinical Research Site

St Louis, Missouri 63136 - United States

Status: RECRUITING

Clinical Research Site

Midlothian, Virginia 23114 - United States

Status: RECRUITING

Clinical Research Site

Richmond, Virginia 23230 - United States

Status: RECRUITING

Clinical Research Site

Richmond, Virginia 23298 - United States

Status: RECRUITING

Clinical Research Site

Mississauga, Ontario L5M 2N1 - Canada

Status: RECRUITING

Clinical Research Site

Oshawa, Ontario L1G 2B9 - Canada

Status: RECRUITING

And 3 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Prostate Cancer:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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