How to Join This Clinical Trial - NCTNCT06315491

Learn how to participate in this PHASE2 trial studying an investigational therapy for Platinum-resistant Ovarian Cancer, Refractory Ovarian Carcinoma. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied

Platinum-resistant Ovarian Cancer, Refractory Ovarian Carcinoma

Treatment Being Tested

Investigational treatment

Study Phase

PHASE2 - Safety and effectiveness study

Enrollment Status

Currently enrolling participants

Study Identifier

NCTNCT06315491 - 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 19 locations. Find a study site near you:

And 9 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 Platinum-resistant Ovarian Cancer, Refractory Ovarian Carcinoma:

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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