GV1001 Subcutaneous(SC) for the Treatment of Progressive Supranuclear Palsy (PSP)

Progressive Supranuclear Palsy Clinical Trial

Official title:

A Multi-center, Randomized, Double-blind, Placebo-controlled, Parallel Design, Prospective, Phase IIa Exploratory Clinical Trial to Evaluate the Efficacy and Safety of SC Administration of GV1001 0.56 or 1.12 mg/Day in Patients With PSP

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05819658
• Other study ID #: GV1001-PSP-CL2-011
• Status: Recruiting
• Phase: Phase 2
• Start date: June 14, 2023
• Est. completion date: May 31, 2024

Study information

• Verified date: April 2023
• Source: GemVax & Kael
• Contact: Mino Moon
• Phone: +82 70 4738 9726
• Email: clinical[@]gemvax.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study will be conducted by the Sponsor to evaluate the efficacy and safety of GV1001 (0.56 mg and 1.12 mg) administered subcutaneously as a treatment for Progressive Supranuclear Palsy, (PSP). In 75 patients diagnosed with PSPR Richardson(PSP-RS) or PSP-Parkinsonism (PSP-P) at five hospitals in Korea, subcutaneous administration of GV1001 0.56 or 1.12 mg/day will be conducted with multicenter, randomized, double-blind, placebo-controlled, parallel design, prospective phase 2a.

Description:

This is a 24-week, multicenter, randomized, double-blind, placebo-controlled, parallel design, prospective, Phase 2a exploratory clinical study. If the subject and/or the subject's representative provide a written consent to participate in this clinical study, the required examinations and tests will be performed at the screening visit, and the screening period will run for 4 weeks or shorter. Subjects who are ultimately determined as eligible by the inclusion/exclusion criteria after screening will be randomized at a 1:1:1 ratio to Study Group 1 (GV1001 0.56 mg/day), Study Group 2 (GV1001 1.12 mg/day), or the placebo group depending on the study site in which they are enrolled. Depending on the randomization results, subjects will be administered the investigational product (study drug or placebo) once weekly for the first 4 weeks (1 month), and then administered 10 times at 2-week intervals for 20 weeks (5 months) for a total of 14 doses over 24 weeks (6 months). All subjects will visit the institution according to the planned clinical study schedule to receive the investigational product and to be evaluated for efficacy and safety. To ensure the objectivity and accuracy of the study results, the individuals evaluating efficacy will be limited to neurologists who have been sufficiently educated and trained, and the collection of efficacy and safety evaluation data and biomarkers will be performed in a consistent order at each visit.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 75
• Est. completion date: May 31, 2024
• Est. primary completion date: December 15, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 41 Years to 85 Years

Eligibility

Inclusion Criteria:

• Patients aged =41 years to = 85 years.

• Clinical diagnosis of probable progressive supranuclear palsy (PSP).

• Patient is on a stable therapy for a neurological drug for at least 1 month prior to screening visit.

• Patients who are able to walk 3 meters or more independently or with assistive devices.

• Score 15 points = on the Korean Mini-Mental Status Exam (K-MMSE) at the screening visit.

• Have reliable caregiver to accompany participant to all study visits.

• Patients and/or their representatives who have voluntarily provided a written consent for participation in this clinical study.

Exclusion Criteria:

• Patients who have Presence of structural lesions or Suspected concurrent onset of central nervous system diseases based on the CT/MRI scan results and neurological examinations performed within 12 months of screening or at screening.

• Patients with a history of known or suspected seizures.

• Patients with a recent unexplained loss of consciousness within 3 months prior to screening or a history of significant head trauma with loss of consciousness.

• Patients with acute or unstable cardiovascular disease, uncontrolled hypertension, uncontrolled diabetes, or any other medical condition that can interfere with completing the clinical study.

• Patients with hypersensitivity reactions to the ingredients of the investigational product.

• Patients with a history of cancer within 5 years prior to screening.

• Patients with abnormal renal function.

• Patients with severe liver function abnormalities.

• Patients weighing =35 kg.

• Among the female subjects who does not agree to use proper contraception.

• Pregnant or breastfeeding women.

• Patients who participated in another clinical study within 4 weeks prior to screening and were administered investigational products or were applied investigational medical devices.

• Patients who were administered the study drug (GV1001) of this clinical study within 12 months prior to screening.

• Patients who participated in a clinical study for progressive supranuclear palsy within 6 months prior to screening.

• Other patients judged by the investigator as ineligible to participate in this clinical study.

Related Conditions & MeSH terms

• Progressive Supranuclear Palsy
• Supranuclear Palsy, Progressive

Intervention

Drug:
• GV1001 Placebo
0.9% normal saline
• GV1001 0.56mg
Lyophilized peptide from hTERT
• GV1001 1.12mg
Lyophilized peptide from hTERT

Locations

Country	Name	City	State
Korea, Republic of	Seoul National University Bundang Hospital	Seongnam-si
Korea, Republic of	Kyung Hee University Hospital	Seoul
Korea, Republic of	Samsung Medical Center	Seoul
Korea, Republic of	Seoul Metropolitan Government Seoul National University Boramae Medical Center	Seoul
Korea, Republic of	Seoul National University Hospital	Seoul

Sponsors (1)

Lead Sponsor	Collaborator
GemVax & Kael

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change from the baseline in the total score of PSP-rating scale	Change from the baseline in the total score of PSP-rating scale(Progressive Supranuclear Palsy Rating Scale) after 24 weeks (6 months) of investigational product administration. The possible total scores range from 0 to 100 with a higher score indicating severely impaired cognitive function.	6 months
Secondary	Change from the baseline in the total score of PSP-rating scale	Change from the baseline in the total score of PSP-rating scale(Progressive Supranuclear Palsy Rating Scale) after 12 weeks (3 months) of investigational product administration. The possible total scores range from 0 to 100 with a higher score indicating severely impaired cognitive function.	3 months
Secondary	Change from the baseline in the Montreal Cognitive Assessment - Korea (MoCAK)	Change from the baseline in the Montreal Cognitive Assessment - Korea (MoCAK) after 12 weeks (3 months) and 24 weeks (6 months) of investigational product administration. The possible total scores range from 0 to 30 with a higher score indicating greater cognitive function.	3 months and 6 months
Secondary	Change from the baseline in the Korean Frontal Assessment Battery (K-FAB)	Change from the baseline in the Korean Frontal Assessment Battery (K-FAB) after 12 weeks (3 months) and 24 weeks (6 months) of investigational product administration. The possible total scores range from 0 to 18 with a higher score indicating greater cognitive function.	3 months and 6 months
Secondary	Change from the baseline in the England & Schwab Activity of Daily Living (ES ADL) scale	Change from the baseline in the England & Schwab Activity of Daily Living (ES ADL) scale after 12 weeks (3 months) and 24 weeks (6 months) of investigational product administration. The possible total scores range from 0 (complete dependence) to 100% (complete independence) based on the level of independence.	3 months and 6 months
Secondary	Change from the baseline in the score of each domain of the PSP-rating scale	Change from the baseline in the score of each domain of the PSP-rating scale(Progressive Supranuclear Palsy Rating Scale) after 12 weeks (3 months) and 24 weeks (6 months) of investigational product administration. Each domain is rated from different range (0 to 8, 16, 20 or 24) with a higher total score indicating severely impaired cognitive function.	3 months and 6 months
Secondary	Change from the baseline in the score of each item of the PSP-rating scale	Change from the baseline in the score of each item of the PSP-rating scale(Progressive Supranuclear Palsy Rating Scale) after 12 weeks (3 months) and 24 weeks (6 months) of investigational product administration. Each item is rated from different range (0 to 2 or 4) with a higher total score indicating severely impaired cognitive function.	3 months and 6 months