TP04HN106 in the Treatment of Patients With Amyotrophic Lateral Sclerosis

Last updated: December 19, 2024
Sponsor: Talengen Institute of Life Sciences, Shenzhen, P.R. China.
Overall Status: Active - Recruiting

Phase

1/2

Condition

Myasthenia Gravis (Chronic Weakness)

Amyotrophic Lateral Sclerosis (Als)

Scar Tissue

Treatment

TP04HN106

Saline

Clinical Study ID

NCT06726577
TP04HN106-ALS-IIT
  • Ages > 18
  • All Genders

Study Summary

This trial adopts a multicenter, randomized, double-blind, placebo-controlled parallel design.

This experiment is divided into two groups: the experimental drug group and the placebo group. Successful participants will be randomly assigned to the two groups, with an expected enrollment of 60 participants. There will be 30 participants in the experimental drug group and 30 participants in the placebo group. During the treatment period, the experimental drug group received intravenous injections of 0.83mL/kg TP04HN106 each time; The placebo group received intravenous injections of 0.83mL/kg of saline each time. During the extension period, all subjects received intravenous injection of 0.83mL/kg TP04HN106. In the experiment, all subjects received Liraglutide tablets as the standard baseline treatment.

The subjects who were successfully screened in the experiment were enrolled in sequence, and the safety, tolerability, efficacy, and pharmacokinetic characteristics of the experimental drug were evaluated after administration. The entire trial includes a screening period of 1 week, a treatment period of 12 weeks (including 3 treatment cycles, each treatment cycle of 4 weeks), an extension period of 12 weeks (including 3 treatment cycles, each treatment cycle of 4 weeks), and a follow-up period of 4 weeks. In addition, some subjects underwent a 1-week single dose PK study before the start of the treatment period; In addition, during the first treatment cycle of the treatment period, some subjects were selected for multiple dosing PK studies.

We plan to conduct a single dose PK study among 12 subjects, with 6 subjects in the experimental group and 6 subjects in the control group; Multiple dose PK studies were conducted among 12 subjects, with 6 subjects in the experimental group and 6 sujects in the control group. It is not allowed for the same subject to participate in both single dose and multiple dose PK studies simultaneously.

The 1st to 12th subjects planned to be enrolled in the trial will undergo a single dose PK study. After the first dose, venous blood will be collected from the 12 subjects according to the blood sample collection requirements, and their PK characteristics will be evaluated. The observation period for single dose administration is one week. After completing the final blood sample collection and safety assessment, the subjects enter the treatment period, extension period, and follow-up period.

The 13th to 24th subjects planned to be enrolled in the trial will undergo multiple dose PK studies. These 12 subjects will have their venous blood collected according to the blood sample collection requirements during the first treatment cycle of the treatment period, and their PK characteristics will be evaluated. After completing the treatment period, the subjects will enter the extension period and follow-up period.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Meet the diagnostic criteria for amyotrophic lateral sclerosis (ALS) (Gold CoastCriteria 2020）;

  2. Age ≥18 years old, male or female;

  3. The amyotrophic lateral sclerosis Function Rating Scale (ALSFRS-R）of pre-visitsubjects should be ≥1 score for dyspnea, upright breathing and respiratorydysfunction;

  4. Pre-randomized subjects received stable dose of riluzole tablets for ≥7 days, andshould maintain the treatment until the last study visit;

  5. Voluntarily participate in clinical trials, sign informed consent, and understandand comply with study procedures.

Exclusion

Exclusion Criteria:

  1. The subject is known to be allergic to the investigational drug or its excipients;

  2. The subject has a disease or injury that interferes with functional assessment orthreatens life, or is accompanied by a serious irreversible disease of the heart,lung, liver, or brain, or is accompanied by a failure of different organs (forpatients with respiratory failure, only patients diagnosed as type I or type IIrespiratory failure are excluded);

  3. The subject has a major mental illness or cognitive dysfunction;

  4. Patients with a history of secondary or above surgery within one month before thescreening period;

  5. The subjects participated in other clinical studies within 1 month;

  6. The subjects are pregnant or lactating women;

  7. Poor compliance or other researchers believe that there are any circumstances thatare not suitable for inclusion.

Study Design

Total Participants: 60
Treatment Group(s): 2
Primary Treatment: TP04HN106
Phase: 1/2
Study Start date:
December 10, 2024
Estimated Completion Date:
April 30, 2027

Connect with a study center

  • The First Affiliated Hospital of Soochow University

    Suzhou, Jiangsu 215000
    China

    Active - Recruiting

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