Phase 3 Parkinson's Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with advanced or returning endometrial cancer (cancer of the lining of the uterus) that has been confirmed through a tissue sample, and whose cancer has a specific biological feature called "proficient mismatch repair" (pMMR) — meaning the cancer's repair system is working normally.
- People whose cancer can be seen and measured (or in some cases just detected) on scans, meeting specific staging criteria as assessed by the trial investigator.
- People who have not previously received systemic (whole-body) treatment for endometrial cancer, with limited exceptions: one prior course of platinum-based chemotherapy given with the intent to cure, prior radiation therapy (with or without chemotherapy used to boost radiation effects) completed more than 2 weeks before the trial starts, or prior hormonal therapy that was stopped at least 1 week before the trial starts.
Who may not be able to join:
- People whose uterine cancer is a specific type called carcinosarcoma, neuroendocrine tumour, endometrial sarcoma, stromal sarcoma, leiomyosarcoma, adenosarcoma, or other sarcoma types.
- People whose endometrial cancer has a biological feature called "mismatch repair deficient" (dMMR) — meaning the cancer's repair system is not working properly.
- People for whom doctors consider surgery to completely remove all tumours, or curative-intent radiation therapy, to be a suitable option at the time of enrolment.
- People who have a history of serious dry eye syndrome, severe disease of the glands along the eyelid edges, severe inflammation of the eyelids, or severe corneal (eye surface) conditions that affect healing.
- People who have active inflammatory bowel disease currently requiring medications that suppress the immune system, or who have a history of inflammatory bowel disease.
- People with serious, uncontrolled heart or blood vessel disease, or uncontrolled disease affecting blood vessels in the brain.
- People who are living with HIV and also have a history of a condition called Kaposi's sarcoma or Multicentric Castleman's Disease.
- People who have previously received certain types of treatments, including: immune checkpoint therapies targeting specific proteins on immune cells (such as anti-PD-1 or anti-PD-L1 agents); certain antibody-drug treatments targeting a protein called TROP-2; or antibody-drug treatments containing a substance called a topoisomerase I inhibitor.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Medical Director, Merck Sharp & Dohme LLC
Phone: 1-888-577-8839
Australian sites
+610298818000
0736478111
0394171344
+610864573333
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
4 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Maintenance Treatment: Progression-Free Survival (PFS); Maintenance Treatment: Overall Survival (OS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 20 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.