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Stem cells injected into brain for Parkinson's: safe?

NCT ID NCT02452723

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This early-phase study tested whether injecting human neural stem cells into specific brain areas is safe for people with Parkinson's disease. Twelve participants received the cell therapy at one of three dose levels. The main goal was to check for side effects, while also looking for any improvement in movement symptoms.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 1

The first testing in people. Mainly checks safety and dose, usually in a small group.

Participants

12 people

The number who actually took part.

Started

Jul 2016

Finished

Sep 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

30 to 70 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Signed informed consent form (ICF) indicating the patient has been informed of the procedures to be followed, the experimental nature of the therapy, alternatives, potential benefits, side-effects, risks, and discomforts * Patient diagnosed with idiopathic PD of ≤ 13 years duration, as defined by the United Kingdom (UK) Parkinson's Disease Society Brain Bank criteria * Outpatients (male and female) 30 - 70 years old. Females must be of non-child bearing potential, or with a negative pregnancy test and not breast-feeding * Patients receiving a stable dose of levodopa for at least 3 months with the expectation that the treatment will remain unchanged throughout the course of the patient's participation in the trial * Patients receiving an anti-parkinsonian treatment at a stable dose for at least 3 months with the expectation that the treatment will remain unchanged throughout the course of the patient's participation in the trial * Hoehn and Yahr stage II-IV during "ON" time * Unified Parkinson's Disease Rating Scale (UPDRS) motor score (Part III) in the "OFF" state ≤ 49 * Positive dopaminergic response of ≥ 33% decrease in UPDRS motor scores between "OFF" and "ON" states at screening, and unequivocal clinical off periods * Patient is experiencing motor fluctuations with at least two cumulative hours of daily "OFF" -time during the waking period, which is measured on at least two consecutive days * History of anti-parkinsonian treatment with sufficient doses of levodopa * Stable, well-controlled concomitant disorders that would not contraindicate general anesthesia or stereotactic neurosurgery * No abnormalities on baseline brain MRI * Insufficient control of PD symptoms or intolerable side effects with optimized oral PD therapy * Montreal Cognitive Assessment (MOCA) score ≥ 26 * Willing to fully comply with all study procedures and requirements of the trial * No surgery for PD or been treated with neuroleptics in the past 6 months except low-dose quetiapine fumarate or clozapine * No significant further improvement with physical therapy/rehabilitation Exclusion Criteria: * Mild cognitive impairment of dementia (MOCA score \< 26) * The extent or severity of the disease is not measurable * Severe dyskinesia in the "OFF" or "ON" states (violent dyskinesias, incompatible with any normal motor task) * Pre-existing medical conditions such as bleeding disorders, septicemia, major cardiovascular, cerebrovascular or psychiatric disease * Any current or relevant previous history of serious, severe or unstable physical or psychiatric illness or medical disorder that may make the participant unlikely to fully complete the study (depression, anxiety, cognitive impairment or impulse control disorder) * Clinically significant abnormal hematologic evaluation (blood count, partial thromboplastin time (PTT)), blood chemistry (glucose, blood urea nitrogen (BUN), creatinine, electrolytes), liver function tests (aspartate aminotransferase (AST), alanine aminotransferase (ALT), gamma glutamyl transpeptidase (GGTP), total protein, bilirubin) * Any active infectious disease of any nature, including clinically active viral infections (seropositive for Human Immunodeficiency Virus (HIV), Hepatitis C Virus (HCV), Hepatitis B Virus (HBV) and Syphilis * Severe obesity * Previous intracranial surgery, including deep-brain stimulation * History of seizures * Substance abuse (recent history of alcohol abuse or other drugs such as barbiturates, cannabinoids and amphetamines) * Use of anti-platelet agents or other anti-coagulants * Signs of any malignant disease * Any use of immunosuppressive drugs * Enrollment in other investigational drug trial or has completed any trial within the last 3 months * Patients that cannot undergo MRI or PET scanning (i.e. patients with implanted pacemakers) * Patients unable to travel to the PET scanning center * Any other condition which clinician regards as making patient unsuitable for trial

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Dept of Neurology, The Royal Melbourne Hospital

    Melbourne, Victoria, 3050, Australia

More trials for these conditions

Other studies related to the condition(s) this trial covers.