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RecruitingPhase 2

Intranasal Insulin and Glutathione as an Add-On Therapy in Parkinson's Disease

Gateway Institute for Brain Research · NCT05266417

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 30+ · All sexes
Healthy volunteers
Not accepted (a condition is required)
Study type
Interventional · Phase 2
Target enrollment
56
US sites recruiting
4
Study start
February 7, 2022
Record last updated
July 22, 2026

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study is about

This study will be evaluating the safety and efficacy of insulin and glutathione in subjects with Parkinson's Disease compared to placebo.

Being studied: INS-GSH; Matched Placebos

Conditions: Parkinson Disease

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Key Inclusion Criteria

  • Documented clinical diagnosis of idiopathic PD
  • Able to administer study drug or have a caregiver throughout the duration of the study to help administer drug
  • Willing to continue diet, exercise and medications reported at baseline consistently throughout participation in the trial. Essential changes are permitted
  • If taking PD medications or any nutraceuticals, must be on a stable dose for at least 30 days prior to Screening Visit. Essential changes will be permitted.
  • If subject is taking chronic antidepressant or an anxiolytic, must be on a stable dose for at least 90 days prior to Screening. Essential changes will be permitted.

Key Exclusion Criteria

  • Clinical diagnosis of Type 1 or Type 2 Diabetes Mellitus
  • Glycated hemoglobin (HbA1c) level ≥ 6.5%
  • History of symptomatic hypoglycemia and/or documented plasma glucose levels of ≤ 50 mg/dL with symptoms of hypoglycemia.
  • Mini-Mental State Exam (MMSE) score of ≤ 24 at Screening
  • Positive COVID-19 test at Screening and/or within 30 days of Screening
  • Change in or escalation of dose of a chronic therapeutic agent that has the potential to impair cognitive functioning per investigator within the last 8 weeks of Screening or during the study conduct.
  • Chronic inflammation of nasal cavity, history of recurrent epistaxis, and/or clinically significant medical history of uncontrolled allergic rhinitis, rhino-conjunctivitis, or house dust mite allergy at Screening that may prevent absorption of study treatments.
  • Insufficiently controlled respiratory disease (i.e., asthma, COPD).
  • History of any significant neurologic or psychiatric disease other than PD
  • Current diagnosis of epilepsy and had a history of seizures as an adult within 1 year of Screening, or unexplained recent loss of consciousness, or history of significant head trauma with loss of consciousness
  • History of non-lacunar ischemic and/or hemorrhagic stroke with residual neurologic deficits.
  • Unstable or uncontrolled cardiac disease that could expose the subject to additional safety risks
  • Use of the following medications: Insulin or any other anti-hyperglycemic agent(s) except if used during isolated gestational diabetes, Supplementation with GSH or any medication shown to increase glutathione

Recruiting US locations

  • Institute for Neuroimmune Medicine

    Davie, FL 33314

    Site contact: Rafael Iglesias · 954-262-2876 · ri73@nova.edu

  • Las Mercedes Medical Research

    Hialeah, FL 33012

    Site contact: Elivra Grana · 786-577-5977 · elvira.grana@lmmresearch.com

  • NextGen Research Group

    Miami, FL 33165

    Site contact: Dayana Rojas, PhD, MPH · 786-427-9659 · dayana.rojas@nextgenresearchgroup.com

  • Charter Research

    The Villages, FL 32162

    Site contact: Alessandra Cuevas · 352-441-2000 · Alessandra.Cuevas@charterresearch.com

Study contacts (from the official record)

  • Susana Restrepo, PhD · 786-216-5334 · srestrepo@gifbr.com
  • Vanesa Javier · 954-636-2166 · vaday@gifbr.com
All diabetes studies in Florida →
Intranasal Insulin and Glutathione as an Add-On Therapy in… (NCT05266417) | Bored Studies