A Clinical Trial of the Safety and Efficacy of TJ0113 Capsules in the Treatment of Patients With Age-related Hearing Loss

NCT07012746 | Not Yet Recruiting DMC

• 1 other identifier: 2024198-1
• Study Type: interventional
• Target: 60
• Locations: 1 country
• Sites: 1

Brief Summary

The purpose of this study is to explore the safety and efficacy of TJ0113 capsules in patients with age-related hearing loss.

Conditions

Age Related Hearing Loss; Deafness

Outcome Measures

Primary Outcomes (1)

• Safety of TJ0113 capsule in the treatment of patients with age-related hearing loss

  Incidence of adverse events in each group

  Baseline, weeks 1, 4, 12, 24, and 1 week after discontinuation

Secondary Outcomes (3)

• Speech Intelligibility - Word Recognition in Quiet and Noise

  From baseline to 4, 12 ,24 weeks

• Pure Tone Audiometry (PTA)

  From baseline to 4, 12 ,24 weeks

• Individual's health-related quality of life (HRQOL)

  From baseline to 4, 12 ,24 weeks

Other Outcomes (7)

• Auditory brainstem response (ABR)

  From baseline to 12 and 24 weeks

• Distortion product otoacoustic emissions (DPOAE)

  From baseline to 12 and 24 weeks

• Tinnitus Assessment

  From baseline to 4, 12 and 24 weeks

Study Arms (2)

TJ0113 group

EXPERIMENTAL

Participants will be treated with TJ0113 capsule 200 mg daily for up to 24 weeks

Drug: TJ0113 capsules

Placebo group

PLACEBO COMPARATOR

Participants will be treated with a placebo 200 mg daily for up to 24 weeks

Drug: Placebo capsules

Interventions

TJ0113 capsules DRUG

Oral intake on an empty stomach in the morning, 200 mg each time, fasting within half an hour after taking. It is recommended to keep the drug at the same time (± 1 h ) of a day .

TJ0113 group

Placebo capsules DRUG

Oral intake on an empty stomach in the morning, 200 mg each time, fasting within half an hour after taking. It is recommended to keep the drug at the same time (± 1 h ) of a day .

Placebo group

Eligibility Criteria

• Age: 65 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Older Adult (65+)

You may qualify if:

• The subjects voluntarily participate in the clinical trial, sign the informed consent form, understand and follow the protocol, and fully understand the test content, process and possible adverse reactions.
• Age between 65 and 80 years (including the critical value)
• A diagnosis of symmetrical sensorineural deafness (SNHL) with a history of\> 3 months (binaural threshold difference in mean PTA frequency \<15 dB HL), the PTA level should be between moderate (\> 35dB) and severe (\<80dB) hearing loss
• Hearing aids have not been used, or otherwise, it should be used regularly for more than 3 years and stopped for 3 months before enrollment.
• Subjects and their partners had no birth plan, sperm or egg donation plans from the screening period until within 6 months after the end of the trial and would voluntarily take effective contraception (e. g. abstinence, condoms, etc.). Male subjects should agree to avoid sperm donation within 6 months from the start of administration until cessation of study treatment. Female subjects should be menopausal (over 24 months).

You may not qualify if:

• The presence of implants in the study ear (such as cochlear implant, artificial hearing bone, etc.);
• Suffering from acute otitis media or other ear infection within the previous 3 months or previous chronic suppurative otitis media or tympanic membrane perforation, or with conductive deafness, previous history of ear trauma or surgery, combined middle ear or inner ear malformation, otosclerosis, Meniere's disease, sudden deafness and no recovery of hearing, all of which will impact results explained.
• Patients with sensorineural deafness caused by non-aging factors (e. g., hereditary deafness, congenital deafness, drug-induced deafness, noise deafness, neurosyphilis, severe retrocochlear lesions or organic lesions), and unilateral deafness
• Occupation that is sensitive to sound: musician, conductor, music teacher, etc.
• Use headphones at high volume or frequent exposure to noise in previous work or life;
• History of alcohol or drug dependence / drug abuse in the last 1 year;
• Positive pregnancy test at screening or at the baseline visit, pregnant, lactating, or planned to become pregnant during the trial
• Failure to swallow oral medication, or, according to the investigator, any conditions that may significantly affect the absorption, distribution, metabolism and excretion of the drug, or that may pose a hazard to the subjects participating in this trial; 9.People who currently taking drugs that can improve symptoms such as dementia and depression 10.Subjects with a severe or unstable systemic disease, such as serious congenital disease, blood disease, endocrine disease, nerve or nervous system disease, end-stage disease, head and neck tumor radiotherapy and chemotherapy history, major surgical treatment, psychological disorders (severe insomnia, severe depression, severe anxiety, etc. diagnosed within the previous 90 days ) or history and clinical significance of abnormal baseline laboratory values, such as hepatic insufficiency (alanine transaminase (ALT) and / or alanine transaminase (AST) is 2 times above the upper limit of the reference range, or renal insufficiency (creatinine clearance Ccr \<30 mL/min), or history of malignant tumors and the detection results of tumor markers during the screening period have clinical significance, or unsuitable participants, as judged by the investigator; 11.Subjects suffering from any one of the following heart diseases: a. having uncontrolled or serious cardiovascular and cerebrovascular disease, including the development of grade II ( New York Heart Association, NYHA) or above congestive heart failure, unstable angina, acute myocardial infarction within 6 months before the first drug administration, or cardiac arrhythmias requiring treatment at screening; With b. hypertension (systolic pressure≥ 160mmHg and / or diastolic v≥ 100mmHg), and after the combination of two or more antihypertensive drugs can not be reduced to the normal range; or c.with a history of clinically significant ECG abnormalities, the QRS time was\> 120ms, Long QT syndrome: QTc interval\> 450ms in male or QTc interval\> 470ms in female.
• Participated in a clinical study involving the administration, device, or surgery of the study drug (new chemical entity) within 90 days or 5 half-lives (whichever is longer) 13.Patients with a previous history of hepatitis B, or any of the following indicators are positive at screening: hepatitis B virus surface antigen (HBsAg), hepatitis C virus (HCV) antibody, human immunodeficiency virus (HIV) antibody, or treponema pallidum antibody.
• The subject is not fit to participate in the study if the investigator considers. Or the subject could not participate in the trial for his own reasons, or the behavior subject may interfere with treatment, study or interpretation of results (e. g., previous treatment with high-dose aminoglycosides).

Sponsors & Collaborators

• Yilai Shu: lead
• Hangzhou PhecdaMed Co., Ltd.: collaborator

Study Sites (1)

Eye & ENT Hospital of Fudan University

Shanghai, Shanghai Municipality, 200031, China

Location

MeSH Terms

Conditions

Presbycusis; Deafness

Condition Hierarchy (Ancestors)

Hearing Loss, Sensorineural; Hearing Loss; Hearing Disorders; Ear Diseases; Otorhinolaryngologic Diseases; Sensation Disorders; Neurologic Manifestations; Nervous System Diseases; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: TRIPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR INVESTIGATOR
• PI Title: Principal Investigator

Study Record Dates

• First Submitted: April 29, 2025
• First Posted: June 10, 2025
• Study Start: June 7, 2025
• Primary Completion (Estimated): December 1, 2026
• Study Completion (Estimated): April 1, 2027
• Last Updated: June 10, 2025

Record last verified: 2025-05

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)