Parkinson's drug study aims to uncover disease clues
NCT ID NCT05677633
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This early-phase study tested the safety of a drug called sargramostim (Leukine) in 11 people with Parkinson's disease over 48 weeks. Researchers also looked for changes in immune cells and other biomarkers that might help track the disease. The goal was not to cure Parkinson's but to better understand how the body responds to treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- sargramostim (Leukine)
- What this could lead to
- If successful, this study could help identify biomarkers that track Parkinson's disease progression and response to treatment, potentially guiding future therapies.
- What could go wrong
- This is a very small, early-phase trial with only 11 participants, focused on safety and biomarker validation rather than proving effectiveness. Results may not apply to all Parkinson's patients.
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
-
11 people
The number who actually took part.
- Started
-
Jan 2023
- Finished
-
Nov 2024
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
35 to 85 years
- Sex
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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 Hide 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: 1. Onset of bradykinesia and 1 or both of the following: rest tremor and/or rigidity 2. Asymmetric onset of clinical signs 3. Progressive motor symptoms 4. Age at onset 35-85 years 5. Duration of PD symptoms of at least 3 years 6. Female subjects must be either: 1. Not pregnant, not breastfeeding, and not planning on becoming pregnant during the study; 2. Not of childbearing potential, defined as one who has been postmenopausal for at least 1 year and with follicle stimulating hormone (FSH) levels in the laboratory defined postmenopausal range, or has been surgically sterilized, or has had a hysterectomy at least 3 months prior to the start of this trial; or 3. If of childbearing potential, must agree to use an effective method of avoiding pregnancy to the end of the trial and must have a negative serum beta-human chorionic gonadotropin (β-HCG) test. Effective methods of avoiding pregnancy are contraceptive methods used consistently and correctly (including implantable contraceptives, injectable contraceptives, oral contraceptives, transdermal contraceptives, intrauterine devices, diaphragm with spermicide, male or female condoms with spermicide, or cervical cap), abstinence, or a sterile sexual partner. 7. Must be stage 4 or less according to the Hoehn and Yahr scale Exclusion Criteria: 1. Atypical features indicative of a Parkinson-Plus disorder (Progressive Supranuclear Palsy (PSP), Multiple System Atrophy (MSA), Corticobasal Degeneration (CBD)) including cerebellar signs, supranuclear gaze palsy, apraxia and other cortical signs, or prominent autonomic failure 2. Neuroleptic treatment at time of onset of parkinsonism 3. Active treatment with a neuroleptic at time of study entry 4. History of repeated strokes with stepwise progression of parkinsonism 5. History of repeated head injury 6. History of definite encephalitis 7. More than one blood relative diagnosed with PD 8. Prominent gait imbalance early in the course (\< 5 years) 9. Mini-mental state examination score \<26 10. Hematological malignancy or coagulopathy 11. Abnormal blood analyses: hematocrit \<30; white blood cell count \>11.5; clinically significant laboratory data (e.g. alanine aminotransferase (ALT) or aspartate aminotransferase (AST) 3x the upper limit of normal (ULN), or any abnormal laboratory value that could interfere with the assessment of safety in the judgment of the investigator; significant abnormalities on the clinical examination, vital signs, and clinical chemistry or hematology results (excluding findings of Parkinson's disease), that may interfere with the study or present a safety risk for the subject as judged by the clinical investigator charged in the care of study participants 12. Serious medical illness or co-morbidity that may interfere with participation in the study 13. Brain surgery for parkinsonism (DBS, cell implantation, gene therapy) 14. History of an autoimmune disorder or systemic inflammatory disorder deemed significant by physician 15. Immunostimulatory or immunosuppressive treatment (including amphetamines or systemic corticosteroids) within 90 days 16. Exclusively unilateral parkinsonism for longer than 3 years 17. Known hypersensitivity to granulocyte-macrophage colony-stimulating factor (GM-CSF), yeast-derived products 18. Current lithium treatment 19. Individuals with current diagnoses of alcohol or substance abuse/dependence 20. Anyone who is not appropriate for participation in this research protocol as deemed by the principal or co-investigator 21. Anyone who has previously been treated with granulocyte-macrophage colony-stimulating factor (GM-CSF) as an immunomodulatory therapy 22. Anyone with poor venous access 23. Anyone who has any illnesses or events that would cause a neurological abnormality, apart from Parkinson's disease. 24. Subjects with allergies or sensitivities to yeast products. 25. Subjects that have received a flu shot within the past 3 weeks.
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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
-
University of Nebraska Medical Center
Omaha, Nebraska, 68198, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a One-Time bone drug shield Parkinson's patients from fractures?
- Parkinson's sleep study: does turning brain stimulation off at night help?
- Tailored brain zaps could help Parkinson's patients walk better
- Walking study for Parkinson's and stroke patients withdrawn before starting
- Online support groups and telemedicine aim to ease Parkinson's and dementia burden