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NCT Number: NCT05266417

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

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

Recruiting

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Key information

Age range

30 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Institute for Neuroimmune Medicine, Davie, Florida, United States

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

INS-GSH

Drug

Intranasal INS-GSH Twice Daily

Matched Placebos

Drug

Intranasal Matched Placebos Twice Daily

Other names: Insulin Matched Placebo and Glutathione Matched Placebo

Primary outcomes

  1. Verbal Fluency

    Time frame: 24 Weeks

    F, A and S (FAS) words test

Secondary outcomes

  1. Verbal Fluency

    Time frame: 28 Weeks

    Change in verbal fluency as assessed by the FAS test

  2. Motor Function

    Time frame: 24 Weeks

    Change in Timed Up and Go (TUG) test

  3. Motor Function

    Time frame: 24 Weeks

    Change in the updated Movement Disorder Society-Sponsored Revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS) Part III total score

  4. Motor Function

    Time frame: 24 Weeks

    Change in the updated MDS-UPDRS total score

  5. Motor Function

    Time frame: Week 24

    Change in the Clinical Global Impression (CGI) score

  6. Motor Function

    Time frame: Week 24

    Change in Clinical Impression of Severity Index for Parkinson's Disease (CISI-PD)

  7. Cognitive Function

    Time frame: Week 24

    Change in each of the individual twelve (12) task standardized scores assessed using the Cambridge Brain Sciences (CBS) computerized neuropsychological battery

  8. Non-Motor Function

    Time frame: Week 24

    Change in Hamilton Rating Scale for Depression total score

  9. Patient Reported Outcome

    Time frame: Week 24

    Change in Parkinson's Disease Quality of Life Questionnaire (PDQ-39) assessment

  10. Patient Reported Outcome

    Time frame: Week 24

    Change in the Patient Global Impression (PGI) score

Study contacts

Contact information is provided by the study sponsor or research team.

Susana Restrepo, PhD

CONTACT

[email protected]

786-216-5334

Vanesa Javier

CONTACT

[email protected]

954-636-2166

Sponsors and collaborators

Lead sponsor

Gateway Institute for Brain Research

Industry

Registry information

Official study title

A Randomized, Double-Blind, Placebo-Controlled, Phase II Study to Evaluate the Safety, Tolerability, and Efficacy of Intranasal Insulin and Glutathione as an Add-On Therapy in Subjects With Parkinson's Disease (NOSE-PD)

Acronym: NOSE-PD

Important dates

Study start
2022
Primary completion
2027
Study completion
2027
First posted
Mar 4, 2022
Registry last updated
Jul 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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