Patient Guide: A Master Protocol Study to Investigate Biomarker-guided Novel Anticancer Agent(s) as Monotherapy or Combination Therapy in Participants With Advanced/Recurrent Ovarian Cancer

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 23 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT07060365
Status: NOT_YET_RECRUITING
Condition: Advanced/Recurrent Ovarian Cancer
Phase: PHASE1, PHASE2

Where You Can Participate

This study is available at 23 locations across the country.

Top locations include:
  • • Fullerton, California
  • • Albuquerque, New Mexico
  • • New York, New York
  • • And 20 more locations

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A Master Protocol Study to Investigate Biomarker-guided Novel Anticancer Agent(s) as Monotherapy or Combination Therapy in Participants With Advanced/Recurrent Ovarian Cancer - Join Clinical Trial NCTNCT07060365

How to Join This Clinical Trial - NCTNCT07060365

Learn how to participate in this PHASE1, PHASE2 trial studying an investigational therapy for Advanced/Recurrent Ovarian Cancer. Current status: NOT_YET_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Advanced/Recurrent Ovarian Cancer
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1, PHASE2 - Safety and effectiveness study
Enrollment Status
NOT_YET_RECRUITING
Study Identifier
NCTNCT07060365 - 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 23 locations. Find a study site near you:

Clinical Research Site

Fullerton, California 92835 - United States

Status: Contact for availability

Clinical Research Site

Albuquerque, New Mexico 87109 - United States

Status: Contact for availability

Clinical Research Site

New York, New York 10016 - United States

Status: Contact for availability

Clinical Research Site

New York, New York 10065 - United States

Status: Contact for availability

Clinical Research Site

Oklahoma City, Oklahoma 73104 - United States

Status: Contact for availability

Clinical Research Site

Sioux Falls, South Dakota 57105 - United States

Status: Contact for availability

Clinical Research Site

Seattle, Washington 98109 - United States

Status: Contact for availability

Clinical Research Site

Milwaukee, Wisconsin 53226 - United States

Status: Contact for availability

Clinical Research Site

Milano, 20132 - Italy

Status: Contact for availability

Clinical Research Site

Milano, 20141 - Italy

Status: Contact for availability

And 13 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, PHASE2 clinical trial for Advanced/Recurrent Ovarian 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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