31P-MRS Imaging to Assess the Effects of CNM-Au8 on Impaired Neuronal Redox State in Parkinson's Disease

Parkinson's Disease Clinical Trial

— REPAIR-PD  

Official title:

A Phase 2, Pilot Open Label, Sequential Group, Investigator Blinded Study of Magnetic Resonance Spectroscopy (31P-MRS) to Assess the Effects of CNM-Au8 for the Bioenergetic Improvement of Impaired Neuronal Redox State in Parkinson's Disease

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03815916
• Other study ID #: CNMAu8.202
• Status: Completed
• Phase: Phase 2
• Start date: December 19, 2019
• Est. completion date: June 7, 2021

Study information

• Verified date: May 2024
• Source: Clene Nanomedicine
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

REPAIR-PD is a single-center open label pilot, sequential group, investigator and patient blinded study to assess the CNS metabolic effects, safety, pharmacokinetics, and pharmacodynamics of CNM-Au8 in patients who have been diagnosed with Parkinson's Disease (PD) within three (3) years of Screening. The primary endpoint is the ratio of the oxidized to reduced form of nicotinamide adenine dinucleotide (NAD+:NADH) measured non-invasively by 31phosphorous magnetic resonance spectroscopy (31P-MRS).

Description:

This is a single-center open label pilot, sequential group, investigator blinded study of the CNS metabolic effects, safety, pharmacokinetics, and pharmacodynamics of CNM-Au8 in patients who have been diagnosed with Parkinson's Disease within three years of Screening. The Sponsor will select a starting treatment dose of CNM-Au8 for the initial treatment. Investigators and patients will be blinded to each cohort's study dose. Upon completion of the first treatment cohort, the Sponsor will select a single dose or two different doses for the subsequent second cohort from a pre-specified dosing selection plan based on the evaluation of the 31P-Magnetic Resonance Spectroscopy (31P-MRS) changes versus baseline in the first cohort. Up to a total of two treatment cohorts may be studied (n=15 patients/cohort, total n=30 patients). All patients will receive daily oral treatment over twelve consecutive weeks during each cohort's Treatment Period.

There will be three study periods per treatment cohort:

1. A six-week screening period (Screening Period);

2. A twelve-week treatment period (Treatment Period);

3. A four-week follow-up period (End-of-Study Assessment).

The primary study outcome, CNS metabolic changes, will be assessed based upon each patient's Week 12 study visit versus the pre-treatment baseline. The primary endpoint is the brain metabolic effects of treatment with CNM-Au8 as assessed by an improvement of 31P-MRS assessment of Brain Tissue Cellular Redox Potential defined by the measured tissue ratio of NAD+:NADH concentrations following 12 weeks of once daily treatment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 13
• Est. completion date: June 7, 2021
• Est. primary completion date: June 7, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 30 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Able to understand and give written informed consent and follow study procedures.

2. Male or female, aged 30 - 80 years or age (inclusive) at the time of PD diagnosis.

3. PD subjects will be recruited in accordance with the MDS Clinical Diagnostic Criteria for

PD:

1. Parkinsonism present (bradykinesia + either rest tremor or rigidity)

2. 2 of the following 4 supportive criteria:

i. Clear and dramatic beneficial response to dopaminergic medication

ii. Presence of levodopa-induced dyskinesias

iii. Rest tremor of a limb

iv. Olfactory loss or cardiac sympathetic denervation seen on prior MIBG SPECT

4. Duration of PD since diagnosis is </= 3 years (inclusive)

5. Modified Hoehn and Yahr stage </= 3

6. Treatment with dopaminergic therapy for at least 12-weeks and with no change in current medications within the prior 6-weeks

Exclusion Criteria:

1. Atypical parkinsonism, including that due to drugs, metabolic disorders, encephalitis, cerebrovascular disease, normal pressure hydrocephalus, or other neurodegenerative disease.

2. The presence of any of the following:

1. Unequivocal cerebellar abnormalities

2. Downward vertical gaze limitation or slowing of downward saccades

3. Diagnosis of behavioral variant frontotemporal dementia or primary progressive aphasia

4. Parkinsonian features restricted to the lower limbs for > 3 years

5. Treatment with dopamine blockers or depleters in a time course consistent with drug-induced parkinsonism

6. Absence of an observable response to high dose levodopa despite moderate disease severity

7. Expert considers a diagnosis of alternative syndrome more likely than PD

8. Rapid progression of gait impairment requiring wheelchair within 5 years of onset

9. Complete absence of progression of motor symptoms over 3 years unless due to treatment

10. Early bulbar dysfunction within the first 5 years since diagnosis

11. Inspiratory respiratory dysfunction (stridor or frequent sighs)

12. Severe autonomic failure in the first 5 years

13. Recurrent falls (>1 per year) because of impaired balance in the first 3 years

14. Disproportionate dystonic anterocollis or hand contractures of hands or feet within 10 years

15. Absence of any of the common non-motor features of PD despite 5 years of disease

16. Otherwise unexplained pyramidal tract signs (weakness, hyperreflexia, or extensor toe signs)

17. Bilateral symmetric parkinsonism

3. Mini-Mental State Exammination (MMSE) score of less than 19.

4. Patient with a history of any clinically significant or unstable medical condition based on the Investigator's judgment.

5. History of human immunodeficiency virus (HIV), hepatitis C (HepC) virus antibody, or hepatitis B (HepB) virus antibody.

6. Based on the investigator's judgment, patients who may have difficulty complying with the protocol and/or study procedures.

7. Patient with clinically significant abnormalities in hematology, blood chemistry, ECG, or physical examination not resolved by the Baseline visit which according to Investigator may interfere with study participation.

8. Patients with clinically significant hepatic or renal dysfunction or clinical laboratory findings that would limit the interpretability of change in liver or kidney function, or those with low platelet counts (<150 x 109 per liter) or eosinophilia (absolute eosinophil count of =500 eosinophils per microliter) at Screening.

9. Patient participating in any other investigational drug trial or using investigational drug (within 12 weeks prior to screening and thereafter)

10. Positive screen for drugs of abuse or known history of alcohol abuse.

11. Women of child-bearing potential, or men, who are unwilling or unable to use accepted methods of birth control for up to 6 months following study participation.

12. Women with a positive pregnancy test, are lactating, or are planning to become pregnant during the study or within 6 months of the end of this trial.

13. Patients with implanted metal objects in their body that may be affected by an MRI procedure.

14. Patients who are claustrophobic or otherwise unlikely to be able to complete the MRI scanning procedures.

15. History of allergy to gold in any form.

16. Patient is considered a suicide risk in the opinion of the Investigator, has previously made a suicide attempt, or is currently demonstrating active suicidal ideation. Subjects with intermittent passive suicidal ideation are not necessarily excluded based on the assessment of the Investigator.

Related Conditions & MeSH terms

• Parkinson Disease
• Parkinson's Disease

Intervention

Drug:
• Gold Nanocrystals
CNM-Au8 is a dark red/purple-colored liquid formulation consisting of a stable suspension of faceted clean surfaced elemental gold nanocrystals in buffered deionized water with a concentration of up to 0.5 mg/mL of gold. The formulation is buffered by sodium bicarbonate present at a concentration of 0.546 mg/mL. There are no other excipients. The drug product is formulated to be taken orally and will be provided in single dose HDPE containers. The study doses vary by the concentration of gold nanocrystals per milliliter in a volume of 60 mL.

Locations

Country	Name	City	State
United States	UT Southwestern	Dallas	Texas

Sponsors (2)

Lead Sponsor	Collaborator
Clene Nanomedicine	University of Texas Southwestern Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Mean Change in 31P-MRS Bioenergetic Metabolite CNS Tissue Concentration of NAD+	Mean change in average CNS concentration of NAD+ [mmol/kg] by treatment group	At 12 Week
Other	Mean Change in 31P-MRS Bioenergetic Metabolite CNS Tissue Concentration of NADH	Mean change in average CNS concentration of NADH [% Fraction] by treatment group	At 12 Week
Other	Mean Change in 31P-MRS Bioenergetic Metabolite CNS Tissue Concentration of Pooled NAD+/NADH	Mean change in average CNS concentration of pooled NAD+/NADH [mmol/kg] by treatment group	At 12 Weeks
Other	Mean Change in 31P-MRS Bioenergetic Metabolite CNS Tissue Concentration of ATP	Mean change in average CNS concentration of ATP [mmol/kg] (as internal reference) by treatment group	At 12 Week
Other	Mean Change in 31P-MRS Bioenergetic Metabolite CNS Tissue Concentration of Phosphocreatine (PCr)	Mean change in average CNS concentration of PCr [mmol/kg] by treatment group	At 12 Week
Other	Mean Change in 31P-MRS Bioenergetic Metabolite CNS Tissue Concentration of Intracellular Inorganic Phosphate (Pi(in))	Mean change in average CNS concentration of Pi(in) [mmol/kg] by treatment group	At 12 Week
Other	Mean Change in 31P-MRS Bioenergetic Metabolite CNS Tissue Concentration of Extracellular Inorganic Phosphate (Pi(ex))	Mean change in average CNS concentration of Pi(ex) [mmol/kg] by treatment group	At 12 Week
Other	Mean Change in 31P-MRS Bioenergetic Metabolite CNS Tissue Concentration of Uridine Diphosphate Glucose (UDPG)	Mean change in average CNS concentration of UDPG [mmol/kg] by treatment group	At 12 Week
Other	Mean Change in 31P-MRS Membrane Component Tissue Concentration of Phosphoethanolamine (PE)	Mean change in average CNS concentration of PE [mmol/kg] by treatment group	At 12 Weeks
Other	Mean Change in 31P-MRS Membrane Component CNS Tissue Concentration of Phosphocholine (PC)	Mean change in average CNS concentration of PC [mmol/kg] by treatment group	At 12 Weeks
Other	Mean Change in 31P-MRS Membrane Component CNS Tissue Concentration of Glycerolphophoethanolamine (GPE)	Mean change in average CNS concentration of GPE [mmol/kg] by treatment group	At 12 Weeks
Other	Mean Change in 31P-MRS Membrane Component CNS Tissue Concentration of Glycerophosphocholine (GPC)	Mean change in average CNS concentration of GPC [mmol/kg] by treatment group	At 12 Weeks
Other	Measures of Gait	Measured by APDM instrumented Timed up and go test.	at 12 weeks
Other	Measures of Balance	Measured by APDM Instrumented Postural Sway Test	at 12 weeks
Other	Measure of Mobility	Measured by APDM instrumented Walk Test	at 12 weeks
Other	Measurements of Global Impression of Disease Improvement	Using Clinician Global Impression Scale. Scale is rated from 1-7, with 1 representing Very much improved and 7 representing very much worse.	at 12 weeks
Other	Measurements of Global Impression of Disease Severity	Using Patient Global Impression Scale. Scale is rated from 1-7, with 1 representing very mush improved, and 7 representing very much worse.	at 12 weeks
Other	Measurements of Disease Progression	Using Unified Parkinson's Disease Rating Scale. The scale is based off of participants symptoms, with a lower value representing a being closer to no impairments.	at 12 weeks
Primary	31P-MRS Redox Ratio	The change in 31P-MRS NAD+/NADH ratio was measured by a partial volume coil that images the parietal and occipital lobes as a single value with respect to the fraction (%) of the nicotinamide adenine dinucleotide (NAD) signal measured as either the oxidized (NAD+) or reduced form (NADH).; The primary endpoint was the mean change from Baseline to Week 12 in the ratio of NAD+ to NADH (NAD+/NADH) in the Intent to Treat population. A paired t-test was used to analyze the mean change from baseline.	Baseline to 12 Weeks