Phase 2 Parkinson's Disease Trial, Recruiting NCT07156773 Sponsor: Guangzhou Novaken Pharm Co., Ltd. Condition: Parkinson's Disease
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Phase 2 Parkinson's Disease Trial, Recruiting

NCT07156773
Recruiting Phase 2

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 aged 30 to 85 years (inclusive)
  • People who have been diagnosed with Parkinson's disease according to the Chinese Diagnostic Criteria for Parkinson's Disease (2016), with a diagnosis of at least 3 years
  • People whose Parkinson's symptoms, during their best medication period ("on" state), fall within a mild-to-moderate range on a standard rating scale (Hoehn-Yahr stages 1 to 3)
  • People whose motor symptoms improve by at least 30% when taking their usual morning dose of levodopa (a standard Parkinson's medication), as measured by a standard motor assessment
  • People who have no plans to conceive or donate sperm from 2 weeks before the first dose until 1 month after the last dose, and who agree to use highly effective contraception during that period
  • People who are able to understand the study requirements, provide written consent freely, and follow the trial procedures throughout the study

Who may not be able to join:

  • People whose movement difficulties are so severe that they would be unable to take part in study procedures
  • People experiencing involuntary movements (dyskinesia) that significantly affect their daily life
  • People with a known allergy or sensitivity to any ingredient in the study drug
  • People who have previously had surgery for Parkinson's disease (such as deep brain stimulation or brain cell transplantation), or who plan to have such surgery during the trial
  • People who have had a cancer diagnosis in the past 5 years, with some exceptions for certain early-stage or fully treated cancers (confirm with trial site)
  • People who have had a serious mental health condition in the past year, such as severe depression, mania, schizophrenia, or who have had thoughts of suicide
  • People the investigating doctor considers unsuitable for receiving medication through the nose — for example, due to severe nasal problems or nasal structural differences
  • People currently taking medications that affect the brain and nervous system (such as sleeping tablets, sedatives, antidepressants, or anti-anxiety medications), unless the dose has been stable for at least 30 days before the screening visit and is expected to remain stable throughout the study
  • People with a history of a significant drop in blood pressure when standing up, or in whom this is identified during screening (defined as a drop of 20 mmHg or more in the top blood pressure number, or 10 mmHg or more in the bottom number, within 3 minutes of standing)
  • People whose blood test results during screening show liver or kidney function outside acceptable limits (confirm with trial site for specific values)
  • People who are pregnant, breastfeeding, or who have a positive pregnancy test at screening
  • People with a history of drug or alcohol misuse in the past year
  • People who have taken part in another clinical trial or received an experimental drug within 1 month before screening, or within 5 times the drug's clearance period — whichever is longer
  • People who the investigating doctor considers unsuitable for any other reason

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 26 July 2026
Phase 2: approximately ~30% 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: +86+13590957282

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 2
Sponsor
Guangzhou Novaken Pharm Co., Ltd.
Registry
ClinicalTrials.gov
Start date
3 September 2025
Est. completion
30 March 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

MDS-UPDRS part III score

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: 26 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