Phase 1 Parkinson's Disease Trial, Recruiting NCT07161414 Sponsor: AstraZeneca Condition: Parkinson's Disease
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Phase 1 Parkinson's Disease Trial, Recruiting

NCT07161414
Recruiting Phase 1

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 an advanced solid tumour (one that has spread to other parts of the body or cannot be surgically removed), confirmed by laboratory testing of tissue or cells.
  • People who have already received at least one prior cancer treatment for the disease being studied in this trial.
  • People whose doctor considers a single immunotherapy drug to be an appropriate treatment option for them.
  • People who are reasonably active and able to care for themselves, with an Eastern Cooperative Oncology Group (ECOG) fitness score of 0 or 1 at the time of joining, with no recent decline in that score (confirm with trial site).
  • People who have a life expectancy of at least 12 weeks at the time of joining.
  • People whose liver, kidneys, bone marrow, and other organs are functioning adequately (confirm with trial site for specific requirements).
  • People who weigh at least 30 kg.

Who may not be able to join:

  • People with severe or poorly controlled serious illnesses that could make participation unsafe or interfere with following the trial's requirements.
  • People who have previously had an organ transplant.
  • People who have had another separate cancer that was active at any point in the last 2 years.
  • People who still have significant side effects from a previous cancer treatment (other than hair loss) that have not returned to a mild level or back to their pre-treatment baseline.
  • People with unstable or symptomatic cancer spread to the brain, or with compression of the spinal cord.
  • People who have had cancer spread to the membranes surrounding the brain or spinal cord.
  • People with an active immune deficiency condition, or active infections including tuberculosis (TB), HIV, or hepatitis A, B, or C.
  • People with a history of significant heart rhythm problems, heart muscle disease, symptomatic heart failure, or a heart attack within the past 6 months.
  • People with poorly controlled ongoing illnesses, including active infections, lung scarring or inflammation (interstitial lung disease), serious gut conditions involving chronic diarrhoea, or active non-infectious skin conditions requiring systemic treatment.
  • People with active or previously diagnosed autoimmune or inflammatory conditions that have required ongoing treatment with steroids or other immune-suppressing medications.
  • People with a known allergy or sensitivity to the study drug (rilvegostomig), hyaluronidase, or any of the other ingredients in the study medications.
  • People who previously had to permanently stop an immunotherapy treatment due to serious side effects from that treatment.
  • People who have received any prior cancer treatment, including immunotherapy, within 28 days before the first planned dose of the study treatment.

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 22 July 2026
Phase 1: approximately ~10% 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

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 1
Sponsor
Registry
ClinicalTrials.gov
Start date
25 November 2025
Est. completion
19 July 2027

Where this trial is recruiting

🇰🇷 South Korea 🇪🇸 Spain 🇬🇧 United Kingdom 🇺🇸 United States

Primary endpoints

Area under the Concentration-time Curve During One Dosing Interval (AUCtau)

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: 22 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