Patient Guide: A Safety and Dose-finding Study of PRL-02 Depot in Men With Advanced Prostate Cancer

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 24 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04729114
Status: 🟢 Enrolling Now
Condition: Prostate Cancer, Metastatic Castration Resistant Prostate Cancer, Metastatic Castration-sensitive Prostate Cancer
Phase: PHASE1

Where You Can Participate

This study is available at 24 locations across the country.

Top locations include:
  • • Tucson, Arizona
  • • Anaheim, California
  • • Santa Rosa, California
  • • And 21 more locations

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A Safety and Dose-finding Study of PRL-02 Depot in Men With Advanced Prostate Cancer - Join Clinical Trial NCTNCT04729114

How to Join This Clinical Trial - NCTNCT04729114

Learn how to participate in this PHASE1 trial studying an investigational therapy for Prostate Cancer, Metastatic Castration Resistant Prostate Cancer, Metastatic Castration-sensitive 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, Metastatic Castration Resistant Prostate Cancer, Metastatic Castration-sensitive 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, Metastatic Castration Resistant Prostate Cancer, Metastatic Castration-sensitive Prostate Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1 - Early safety study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT04729114 - 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 24 locations. Find a study site near you:

Clinical Research Site

Tucson, Arizona 85715 - United States

Status: RECRUITING

Clinical Research Site

Anaheim, California 92801 - United States

Status: RECRUITING

Clinical Research Site

Santa Rosa, California 95403 - United States

Status: RECRUITING

Clinical Research Site

Tampa, Florida 33609 - United States

Status: RECRUITING

Clinical Research Site

Fort Wayne, Indiana 46804 - United States

Status: RECRUITING

Clinical Research Site

Jeffersonville, Indiana 47130 - United States

Status: RECRUITING

Clinical Research Site

Wichita, Kansas 67226 - United States

Status: RECRUITING

Clinical Research Site

Towson, Maryland 21204 - United States

Status: RECRUITING

Clinical Research Site

Omaha, Nebraska 68130 - United States

Status: COMPLETED

Clinical Research Site

Morristown, New Jersey 07960 - United States

Status: RECRUITING

And 14 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE1 clinical trial for Prostate Cancer, Metastatic Castration Resistant Prostate Cancer, Metastatic Castration-sensitive 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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