Patient Guide: A Study to Learn About the Investigational Medicine Called PF-06821497 (Mevrometostat) in Men With mCRPC Who Were Previously Treated With Abiraterone Acetate for Prostate Cancer (MEVPRO-1).

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 221 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06551324
Status: 🟢 Enrolling Now
Condition: Metastatic Castrate Resistant Prostate Cancer (mCRPC)
Phase: PHASE3

Where You Can Participate

This study is available at 221 locations across the country.

Top locations include:
  • • Homewood, Alabama
  • • Chandler, Arizona
  • • Gilbert, Arizona
  • • And 218 more locations

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A Study to Learn About the Investigational Medicine Called PF-06821497 (Mevrometostat) in Men With mCRPC Who Were Previously Treated With Abiraterone Acetate for Prostate Cancer (MEVPRO-1). - Join Clinical Trial NCTNCT06551324

How to Join This Clinical Trial - NCTNCT06551324

Learn how to participate in this PHASE3 trial studying an investigational therapy for Metastatic Castrate Resistant Prostate Cancer (mCRPC). This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Metastatic Castrate Resistant Prostate Cancer (mCRPC)
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06551324 - 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 221 locations. Find a study site near you:

Clinical Research Site

Homewood, Alabama 35209 - United States

Status: RECRUITING

Clinical Research Site

Chandler, Arizona 85224 - United States

Status: RECRUITING

Clinical Research Site

Gilbert, Arizona 85297 - United States

Status: RECRUITING

Clinical Research Site

Glendale, Arizona 85306 - United States

Status: RECRUITING

Clinical Research Site

Mesa, Arizona 85202 - United States

Status: RECRUITING

Clinical Research Site

Mesa, Arizona 85206 - United States

Status: RECRUITING

Clinical Research Site

Phoenix, Arizona 85028 - United States

Status: RECRUITING

Clinical Research Site

Scottsdale, Arizona 85260 - United States

Status: RECRUITING

Clinical Research Site

Tucson, Arizona 85741 - United States

Status: RECRUITING

Clinical Research Site

Anaheim, California 92801 - United States

Status: NOT_YET_RECRUITING

And 211 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 Metastatic Castrate Resistant Prostate Cancer (mCRPC):

  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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