Patient Guide: A Study to Learn How Safe the Study Treatment Actinium-225-macropa-pelgifatamab (BAY3546828) is, How it Affects the Body, How it Moves Into, Through and Out of the Body, and About Its Anticancer Activity in Participants With Advanced Metastatic Castration-resistant Prostate Cancer (mCRPC)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 30 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06052306
Status: 🟢 Enrolling Now
Condition: Metastatic Castration-resistant Prostate Cancer
Phase: PHASE1

Where You Can Participate

This study is available at 30 locations across the country.

Top locations include:
  • • Duarte, California
  • • Minneapolis, Minnesota
  • • Omaha, Nebraska
  • • And 27 more locations

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A Study to Learn How Safe the Study Treatment Actinium-225-macropa-pelgifatamab (BAY3546828) is, How it Affects the Body, How it Moves Into, Through and Out of the Body, and About Its Anticancer Activity in Participants With Advanced Metastatic Castration-resistant Prostate Cancer (mCRPC) - Join Clinical Trial NCTNCT06052306

How to Join This Clinical Trial - NCTNCT06052306

Learn how to participate in this PHASE1 trial studying an investigational therapy for Metastatic Castration-resistant Prostate Cancer. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Metastatic Castration-resistant 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
Metastatic Castration-resistant Prostate Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1 - Early safety study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06052306 - 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 30 locations. Find a study site near you:

Clinical Research Site

Duarte, California 91010 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Minneapolis, Minnesota 55455 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Omaha, Nebraska 68130 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Houston, Texas 77030-4000 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Salt Lake City, Utah 84106-1494 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Edmonton, Alberta T6G 1Z2 - Canada

Status: SUSPENDED

Clinical Research Site

Vancouver, British Columbia V5Z 4E6 - Canada

Status: SUSPENDED

Clinical Research Site

Hamilton, Ontario L8V 5C2 - Canada

Status: NOT_YET_RECRUITING

Clinical Research Site

Toronto, Ontario M5G 2C4 - Canada

Status: NOT_YET_RECRUITING

Clinical Research Site

Montreal, Quebec H2X 3E4 - Canada

Status: NOT_YET_RECRUITING

And 20 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 Metastatic Castration-resistant 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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