Research of SORD-CMT Natural History and Epalrestat Treatment

Sponsor
The Third Xiangya Hospital of Central South University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05777226
Collaborator
(none)
30
2
36

Study Details

Study Description

Brief Summary

Charcot-Marie-Tooth disease (CMT) is a group of the most common hereditary peripheral neuropathy with high clinical and genetic heterogeneity. Biallelic pathogenic variants in SORD gene leading to loss of function of SORD protein cause axonal degeneration. Current research suggests that SORD-CMT2 may be the most common subtype of AR-CMT2. The primary purpose of this study is to explore the natural history of SORD-CMT2 patients by detecting the ONLS scale score and serum sorbitol level changes at 6th, 12th, 24th, and 36th months and to evaluate the effectiveness and safety of epalrestat. Patients with strong treatment willingness and voluntary purchase of drugs are included in the epalrestat treatment group, and patients without drug treatment willingness are included in the control group. Patients in the drug treatment group take epalrestat (50 mg) orally three times daily. This study is expected to be carried out simultaneously in 5 hospitals in mainland China. About 30 SORD-CMT2 patients will be enrolled in this study, and the study period will be 36 months.

Condition or Disease Intervention/Treatment Phase
Phase 2

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Multi-center Study of Natural History of SORD-related Charcot-Marie-Tooth Disease and Epalrestat Treatment
Anticipated Study Start Date :
Mar 1, 2023
Anticipated Primary Completion Date :
Mar 1, 2026
Anticipated Study Completion Date :
Mar 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Epalrestat treatment group

Epalrestat;Tablet; 50mg; three times a day; 36 months

Drug: Epalrestat
Patients in the treatment group are intervened with Epalrestat tablets.
Other Names:
  • Epalrestat Tablets(YANGTZE River Pharmaceutical Group Nanjing Pharmaceutical. Co., Ltd.)
  • No Intervention: control group

    No Intervention

    Outcome Measures

    Primary Outcome Measures

    1. Serum sorbitol levels [36 months]

      Changes of serum sorbitol levels at 6, 12, 24 and 36 months

    2. Overall Neuropathy Limitations Scale (ONLS) scores [36 months]

      Changes in ONLS scale scores at 6, 12, 24, and 36 months, The total score for the arm is 5 points and 7 for the leg; the total score ranges from 0 points (no disability) to 12 points (disability)

    Secondary Outcome Measures

    1. The 10-meter walk test (10MWRT) [36 months]

      Changes in the 10-meter walk test (10MWRT) at 6, 12, 24, and 36 months

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    14 Years to 50 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Genetically confirmed SORD-CMT2 patients.

    • Male or non-pregnant, non-lactating female patients, aged > 14 and ≤ 50 years old.

    • Rule out secondary peripheral neuropathy (e.g., diabetic peripheral neuropathy)

    • Voluntarily participate in clinical trials, sign informed consent, and be able to understand and abide by research procedures.

    P.S. Patients who have a strong willingness to treat and voluntarily purchase epalrestat for treatment (50mg, three times a day) are included in the treatment group.

    Exclusion Criteria:
    • Presence of any other cause of peripheral neuropathy.

    • Subjects with other neurological disorders affecting the evaluation of study treatment.

    • History of clinically significant unstable medical disease that may cause harm to subjects participating in this study within the past 1 year.

    • Patients with major trauma or extremity surgery before enrollment or planned for extremity surgery before completion of follow-up.

    • Patients with previous bilateral ankle stabilization surgery.

    • Patients who were treated with other related drugs in the 3 months before enrollment.

    • Have any history of drug abuse; have a history of alcohol dependence in the past 3 months.

    • Subjects who are positive for syphilis antibody and HIV antibody.

    • Subjects whose chest X-ray and B-ultrasound show tumors.

    • Patients with poor compliance and unable to complete the study follow-up.

    • Patients who do not agree to participate in the study.

    • Other factors are not suitable for inclusion.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • The Third Xiangya Hospital of Central South University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ruxu Zhang, Director, Chief physician of Neurology, The Third Xiangya Hospital of Central South University
    ClinicalTrials.gov Identifier:
    NCT05777226
    Other Study ID Numbers:
    • quick22474
    First Posted:
    Mar 21, 2023
    Last Update Posted:
    Mar 24, 2023
    Last Verified:
    Mar 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 24, 2023