Patient Guide: Ocular Assessments in Patients Treated With Tivdak® in Recurrent or Metastatic Cervical Cancer

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 25 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06952660
Status: 🟢 Enrolling Now
Condition: Cervical Cancer
Phase: PHASE4

Where You Can Participate

This study is available at 25 locations across the country.

Top locations include:
  • • Aventura, Florida
  • • Coral Springs, Florida
  • • Deerfield Beach, Florida
  • • And 22 more locations

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Ocular Assessments in Patients Treated With Tivdak® in Recurrent or Metastatic Cervical Cancer - Join Clinical Trial NCTNCT06952660

How to Join This Clinical Trial - NCTNCT06952660

Learn how to participate in this PHASE4 trial studying an investigational therapy for Cervical Cancer. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Cervical Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE4 - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06952660 - 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 25 locations. Find a study site near you:

Clinical Research Site

Aventura, Florida 33180 - United States

Status: RECRUITING

Clinical Research Site

Coral Springs, Florida 33065 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Deerfield Beach, Florida 33064 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Fort Lauderdale, Florida 33308 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Fort Lauderdale, Florida 33316 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Miami, Florida 33133 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Miami Beach, Florida 33140 - United States

Status: RECRUITING

Clinical Research Site

Miami Beach, Florida 33140 - United States

Status: RECRUITING

Clinical Research Site

Orlando, Florida 32806 - United States

Status: RECRUITING

Clinical Research Site

Orlando, Florida 32806 - United States

Status: RECRUITING

And 15 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE4 clinical trial for Cervical 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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