Patient Guide: Safety and Efficacy of Retifanlimab (INCMGA00012) Alone or in Combination With Other Therapies in Participants With Advanced or Metastatic Endometrial Cancer Who Have Progressed on or After Platinum-based Chemotherapy.

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 65 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04463771
Status: ACTIVE_NOT_RECRUITING
Condition: Endometrial Neoplasms
Phase: PHASE2

Where You Can Participate

This study is available at 65 locations across the country.

Top locations include:
  • • Anchorage, Alaska
  • • Phoenix, Arizona
  • • Tucson, Arizona
  • • And 62 more locations

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Safety and Efficacy of Retifanlimab (INCMGA00012) Alone or in Combination With Other Therapies in Participants With Advanced or Metastatic Endometrial Cancer Who Have Progressed on or After Platinum-based Chemotherapy. - Join Clinical Trial NCTNCT04463771

How to Join This Clinical Trial - NCTNCT04463771

Learn how to participate in this PHASE2 trial studying an investigational therapy for Endometrial Neoplasms. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Endometrial Neoplasms
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04463771 - 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 65 locations. Find a study site near you:

Clinical Research Site

Anchorage, Alaska 99508 - United States

Status: Contact for availability

Clinical Research Site

Phoenix, Arizona 85016 - United States

Status: Contact for availability

Clinical Research Site

Tucson, Arizona 85711 - United States

Status: Contact for availability

Clinical Research Site

Los Angeles, California 90048 - United States

Status: Contact for availability

Clinical Research Site

Sylmar, California 91342 - United States

Status: Contact for availability

Clinical Research Site

Fort Lauderdale, Florida 33316 - United States

Status: Contact for availability

Clinical Research Site

Miami Beach, Florida 33140 - United States

Status: Contact for availability

Clinical Research Site

Miami, Florida 33176 - United States

Status: Contact for availability

Clinical Research Site

Orlando, Florida 32804 - United States

Status: Contact for availability

Clinical Research Site

Tampa, Florida 33612-9497 - United States

Status: Contact for availability

And 55 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2 clinical trial for Endometrial Neoplasms:

  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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