A Study to Assess the Efficacy and Safety of Vutiglabridin in Early Parkinson's Disease Patients

Glaceum

Status and phase: Enrolling; Phase 2

Conditions: Parkinson Disease

Treatments: Drug: Vutiglabridin; Drug: Placebo

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT06329141

HSG4112-P2-03

Details and patient eligibility

About

1. Study Objective

   • To assess the efficacy and safety of vutiglabridin in early Parkindson's disease patients

2. Background Glaceum Inc. has evaluated the safety, tolerability, and pharmacokinetic/pharmacodynamic properties of vutiglabridin in healthy subjects through its Phase 1 trials, and is planning to perform this Phase 2a trial to assess the efficacy and safety of vutiglabridin in early Parkinson's disease patients.

3. Study Design and Protocol This study is a randomized, double-blind, placebo-controlled, parallel-group trial. Subjects deemed eligible to participate in this study based on the inclusion/exclusion criteria will be assigned a subject number and randomized to one of the 3 treatment groups - 1 group receiving a placebo - in a 1:1:1 ratio. Subjects will be randomized to double-blind treatments and will receive a once-daily oral dose of the investigational product for 24 weeks according to the study protocol. Several parameters (i.e., MDS-UPDRS, CGI-C, K-NMSS, modified Hoehn-Yahr stage and SNBR) will be evaluated to assess the efficacy of vutiglabridin. Assessments including measurement of vital signs, 12-lead ECG, clinical laboratory test, pregnancy test, physical examination, and adverse event monitoring will be performed to evaluate the safety and tolerability of vutiglabridin. Blood samples will be collected for pharmacokinetic assessment.

Enrollment: 90 estimated patients

Sex: All

Ages: 40 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Able to read, understand, and provide written consent for the trial, comply with the clinical trial protocol, and communicate any adverse events (AEs) and other clinically significant information to the investigator (able to complete the evaluation, including walking or using walking aids).

2. Adult men and women between the ages of 40 and 75 at Screening.

3. Diagnosed with Parkinson's disease according to the UK Parkinson's Disease Society (UKPDS) Brain Bank clinical diagnostic criteria and confirmed the reduction of dopamine transporter on 18F-FP-CIT PET imaging at Screening.

4. Diagnosed with Parkinson's disease within the last 24 months.

5. Hoehn-Yahr stage ≤ 2

6. Eligible females will be:

   • females of childbearing potential who are not pregnant, evidenced by a negative serum hCG pregnancy test at Screening

   • non-lactating, or

   • surgically sterile (defined as documented bilateral tubal ligation, bilateral tubal occlusion, bilateral oophorectomy, hysterectomy) or postmenopausal.

     • Definition of menopause

   • 50 years or over: 12 or more consecutive months without menstruation, in the absence of other conditions.

   • Less than 50 years: FSH level is > 40 IU/L and 12 or more consecutive months without menstruation, in the absence of other conditions.

Exclusion criteria

1. Clinically significant new illness, per Investigator judgment, in the 4 weeks before Screening and during the screening period.

2. Global Deterioration Scale (GDS) ≥ 4 at Screening.

3. Have clinically significant depression as indicated by a Korean Beck Depression Inventory II score (K-BDI-II) > 18 at Screening.

4. BMI less than 18.5 kg/m2 at Screening.

5. Have the following laboratory test results:

   • Clinically significant abnormal hepatic (i.e., AST or ALT greater than 2.5x ULN, or total bilirubin greater than 2x ULN, unless documented Gilbert's syndrome)
   • Renal function laboratory test (i.e., GFR < 60 mL/min).

6. Have the following medical history:

   • Diagnosed with or suspected to have *Parkinson-plus syndromes (PPS)

     • PPS: Multiple System Atrophy, Progressive Supranuclear Palsy, Corticobasal Degeneration, Diffuse Lewy Body Disease, etc.

   • Tremor-dominant Parkinson's disease, per Investigator judgment.

   • Symptoms or signs indicative of neurological functional impairment or known abnormalities in brain CT or MRI imaging.

   • A history of severe heart failure (NYHA class III ~ IV), stroke, cerebral ischemic attacks, or seizures within the past year before screening; or those with a history of myocardial infarction or unstable angina within the last 6 months before screening.

   • Have undergone surgery for Parkinson's disease treatment (e.g., cholecystectomy, deep brain stimulation, fetal tissue transplantation) or any other major brain surgery.

   • Diagnosed with malignant tumors within the past 5 years before screening (except for adequately treated basal cell carcinoma, cervical intraepithelial neoplasia, thyroid cancer, or flat epithelial atypia).

   • Diagnosed with secondary Parkinsonism (drug-induced Parkinsonism, normal pressure hydrocephalus, vascular Parkinsonism).

7. Have swallowing problems

8. Have clinically significant dizziness, nausea, per Investigator's judgment.

9. Currently taking any of the following medications and have the willingness and ability to continue taking them throughout the clinical trial period:

   • Within the 4 weeks before baseline, taking any Parkinson's disease medications, including dopamine agonists, dopamine-depleting enzyme inhibitors [monoamine oxidase inhibitors (MAOi), COMT (catechol-O-methyltransferase) inhibitors], non-dopaminergic drugs (anticholinergic agents, amantadine, etc.), and others PD medications (In case of irreversible MAO-B inhibitor, within the 90 days before baseline)
   • Within the 12 weeks before screening, have used systemic steroids continuously for 7 days or longer.
   • Within the 12 weeks before baseline, taking levodopa or levodopa combinations (except history of levodopa use for more than 4 weeks)
   • Currently taking medications known to be substrates of breast cancer resistant protein (BCRP) at screening (e.g., rosuvastatin, serpalan, etc.) (Note: If switched to another drug of the same class, the subject may be eligible for inclusion).
   • taking of any medication within 6 months of Screening that can alter reproductive hormone levels, either as the intended effect or as a side effect, including: anabolic steroids, androstenedione, bicalutamide, cimetidine, dehydroepiandrosterone, diethylstilbestrol, other estrogens, dutasteride, finasteride, glucocorticoids (e.g., prednisone, cortisone, hydrocortisone, and decadron), oral ketoconazole, megestrol acetate, opiates (e.g., morphine, codeine, oxycodone, hydrocodone), spironolactone, testosterone or any androgen, and any medications for treating prostate cancer.

10. Have taken of stable doses of levodopa or levodopa combination

11. Have known or suspected intolerance to PET scan or fluoropropyl-CIT (18F).

12. Have a history of organ transplantation.

13. Tested positive for HBsAg, HCV Ab, HIV Ag/Ab, or VDRL(RPR) antibodies in screening tests.

14. Known hypersensitivity or contraindication to the main ingredient and excipients of the investigational product.

15. Anticipated to undergo surgery during the clinical trial period or to receive surgical interventions that may affect the completion of the trial or compliance with the clinical trial protocol.

16. Participated in a clinical trial for an investigational drug or medical device for a period equal to or longer than five times the drug's half-life at baseline or within the past 12 weeks, whichever is longer.

17. Unwilling, or whose partner is unwilling, to use a medically acceptable means of *contraception during and for 90 days following completion/withdrawal of the study.

    • Medically acceptable contraceptive methods include:

      • intrauterine device that has been proven highly effective, used by the subject or the subject's spouse/partner
      • physical contraception (male or female) used with chemical sterilization surgical sterilization of the subject or the subject's partner (e.g., vasectomy, hysterectomy, tubal ligation, salpingectomy
      • oral hormonal contraceptive used by the spouse/partner of male subject.

18. Within the last 2 years before screening or during the screening period, have a history of alcohol or drug abuse, or have tested positive for drug use during the screening period (Note: Subjects who have used drugs for the purpose of chronic pain treatment, have documented records of medical history and concomitant medications, may, at the investigator's discretion and with the sponsor's approval, be eligible for inclusion as trial subjects).

19. Deemed unsuitable for participation in the clinical trial by the investigator due to reasons including clinical laboratory test results and other factors.

20. Participating in a non-interventional clinical study that may affect the safety or efficacy assessment of subjects in this clinical trial.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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90 participants in 3 patient groups, including a placebo group

Vutiglabridin 400 mg Multiple Dose

Experimental group

Description:

Multiple oral dosing of vutiglabridin 400 mg for 24 weeks

Treatment:

Drug: Vutiglabridin

Vutiglabridin 800 mg Multiple Dose

Experimental group

Description:

Multiple oral dosing of vutiglabridin 800 mg for 24 weeks

Treatment:

Drug: Vutiglabridin

Placebo

Placebo Comparator group

Description:

Multiple oral dosing of placebo

Treatment:

Drug: Placebo