Phase 3 Parkinson's Disease Trial, Recruiting NCT06952504 Sponsor: Merck Sharp & Dohme LLC Condition: Parkinson's Disease
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Phase 3 Parkinson's Disease Trial, Recruiting

NCT06952504
Recruiting Phase 3 🇦🇺 Australian site

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 20 July 2026
Phase 3: approximately ~65% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Medical Director, Merck Sharp & Dohme LLC

Phone: 1-888-577-8839

Australian sites

Blacktown Hospital ( Site 0201), Blacktown, New South Wales
+610298818000
Royal Brisbane and Women's Hospital ( Site 0206), Brisbane, Queensland
0736478111
Epworth Freemasons ( Site 0207), Melbourne, Victoria
0394171344
Sir Charles Gairdner Hospital ( Site 0203), Nedlands, Western Australia
+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

Status
Recruiting
Phase
Phase 3
Registry
ClinicalTrials.gov
Start date
22 May 2025
Est. completion
24 May 2032

Where this trial is recruiting

🇦🇷 Argentina 🇦🇺 Australia 🇦🇹 Austria 🇧🇪 Belgium 🇧🇷 Brazil 🇨🇦 Canada 🇨🇱 Chile 🇨🇳 China 🇨🇴 Colombia 🇨🇿 Czechia 🇩🇰 Denmark 🇫🇮 Finland 🇫🇷 France 🇩🇪 Germany 🇬🇷 Greece 🇭🇺 Hungary 🇮🇪 Ireland 🇮🇱 Israel 🇮🇹 Italy 🇯🇵 Japan 🇲🇽 Mexico 🇳🇱 Netherlands 🇳🇴 Norway 🇵🇪 Peru 🇵🇱 Poland Puerto Rico 🇸🇬 Singapore 🇰🇷 South Korea 🇪🇸 Spain 🇸🇪 Sweden 🇹🇼 Taiwan 🇹🇭 Thailand 🇬🇧 United Kingdom 🇺🇸 United States

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?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov