Phase 3 Parkinson's Disease Trial, Recruiting NCT06989112 Sponsor: AstraZeneca Condition: Parkinson's Disease
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Phase 3 Parkinson's Disease Trial, Recruiting

NCT06989112
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 are 18 years of age or older at the time of screening (other age rules may also apply depending on local regulations)
  • People who have been diagnosed with a specific type of uterine (endometrial) cancer confirmed by a tissue sample — all subtypes are allowed except sarcomas, though carcinosarcomas are allowed
  • People who have advanced endometrial cancer (Stage III or IV) or cancer that has come back for the first time after surgery or a biopsy, meeting specific staging conditions (confirm with trial site)
  • People whose cancer tests positive for a protein called HER2 at a level of 3+ or 2+, confirmed by central laboratory testing arranged by the trial
  • People whose cancer tests positive for a feature called pMMR (meaning certain DNA repair proteins are working normally), confirmed by central laboratory testing
  • People who can provide a suitable tumour tissue sample from a lesion that has not been treated with radiation, for central laboratory testing
  • People who have not yet received treatment for advanced or recurrent disease, though one prior course of chemotherapy or chemoradiation given with the intention of cure is allowed — provided the cancer came back or progressed at least 6 months after the last chemotherapy dose; prior use of a drug called trastuzumab in that earlier setting is also allowed
  • People who have never received certain types of cancer treatments called ADCs (antibody-drug conjugates), immune checkpoint inhibitors, or therapeutic cancer vaccines
  • People who may have had prior radiation therapy for endometrial cancer (including pelvic, extended field, or internal radiation), provided enough time has passed since treatment
  • People with a general health and activity level rated 0 or 1 on a standard oncology scale, meaning they are fully active or have only minor restrictions on physical activity (confirm with trial site)
  • People whose heart pumping function (left ventricular ejection fraction) is at least 50%, measured within 28 days before joining the trial
  • People whose organ function and blood counts meet required levels, tested within 14 days before joining the trial

Who may not be able to join:

  • People who have had an organ transplant at any point
  • People with ongoing or poorly controlled illness, including active infections, serious long-term gut conditions involving diarrhoea, or active non-infectious skin disease that requires systemic (whole-body) treatment
  • People with spinal cord compression or active cancer spread to the brain or central nervous system
  • People who have had a heart attack within the 6 months before joining, or who have significant heart failure, clinically important irregular heartbeat, or any form of heart muscle disease; people with elevated troponin levels (a heart marker) at screening will need a cardiology review before enrolment
  • People with a history of lung inflammation (ILD/pneumonitis) that was not caused by infection and required steroid treatment, or who currently have or are suspected to have this condition
  • People with certain lung-related conditions, including blood clots in the lungs within the past 3 months, severe asthma, severe chronic obstructive pulmonary disease (COPD), restrictive lung disease, or significant fluid around the lungs
  • People with autoimmune, connective tissue, or inflammatory conditions where lung involvement is confirmed or suspected
  • People who have had a complete surgical removal of one lung
  • People with active or previously documented autoimmune or inflammatory conditions that have required ongoing treatment with steroids or other immune-suppressing medications
  • People with active immune system deficiencies or certain active infections, including tuberculosis, poorly controlled HIV, or active or chronic hepatitis B or C (though people with chronic hepatitis B who are on antiviral treatment with normal liver function and controlled viral levels may be considered)
  • People who are currently receiving other cancer treatments without having had an adequate break beforehand (hormone therapy for non-cancer reasons, such as hormone replacement therapy, is allowed)

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 27 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

Phone: 1-877-240-9479

Australian sites

Research Site, Blacktown,
Research Site, East Melbourne,
Research Site, Nedlands,
Research Site, South Brisbane,

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
Sponsor
Registry
ClinicalTrials.gov
Start date
27 March 2025
Est. completion
19 January 2029

Where this trial is recruiting

🇦🇺 Australia 🇦🇹 Austria 🇧🇪 Belgium 🇧🇷 Brazil 🇨🇦 Canada 🇨🇳 China 🇩🇰 Denmark 🇫🇮 Finland 🇫🇷 France 🇩🇪 Germany 🇭🇺 Hungary 🇮🇹 Italy 🇯🇵 Japan 🇳🇱 Netherlands 🇳🇴 Norway 🇵🇱 Poland 🇰🇷 South Korea 🇪🇸 Spain 🇸🇪 Sweden 🇨🇭 Switzerland 🇹🇼 Taiwan 🇬🇧 United Kingdom 🇺🇸 United States

4 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Progression-free survival (PFS), as assessed by BICR

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: 27 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