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Safety, Tolerability, Efficacy of EA0010 in OTOF Patients With CI

10 agosto 2026 aggiornato da: Shanghai EmayGene Technology Co., Ltd

The Safety, Tolerability, and Efficacy of EA0010 in Patients With OTOF Mutations-Related Hearing Loss Who Have Received Cochlear Implantation

This study will evaluate the safety, tolerability, and efficacy of EA0010 injection in patients with OTOF-related hearing loss who have already undergone cochlear implantation. Conventional gene therapy generally excludes cochlear implant recipients, based on the concern that the electrode array may compromise the reparative potential of inner ear cells. To further address this clinical issue, the present study is designed to enroll cochlear implant users and administer a single intratympanic injection of EA0010 through the stapes annular ligament into the implanted cochlea. One subject is planned to be enrolled, and post-administration assessments of both safety and efficacy will be performed.

Panoramica dello studio

Stato

Attivo, non reclutante

Intervento / Trattamento

Descrizione dettagliata

This study is a single-center, single-arm, open-label, non-randomized clinical study.

To prevent or mitigate potential immune responses to EA0010, participants will receive daily oral or intravenous dexamethasone (0.3 mg/kg) for nine consecutive days, from 3 days before to 5 days after administration (day -3 to day 5). Investigators may adjust the duration and dosage based on clinical requirements. Participants may be admitted to hospital between Day -3 and Day -1. On the day of surgery (Day 0), EA0010 will be administered via intratympanic injection through the stapes annular ligament into the cochlea under aseptic conditions. Participants will receive adeno-associated virus (AAV) at a dose of 2.0×1011 vg/ear/total virus via unilateral cochlear injection (EA0010 Injection is supplied as Solution A and Solution B, each with a titer of 2.0×1013 vg/mL or subject to the actual labeled titer; the two solutions will be mixed at a 1:1 ratio prior to cochlear injection, with a total volume of 10-40 μL); Participants will be closely monitored for 10 days after cochlear injection, may return home after surgical recovery, and will then undergo a 52-week follow-up; the clinical study will end after the last follow-up visit. Subsequent annual follow-ups may be conducted as needed.

Participants will return to the hospital for safety and efficacy assessments at the time points specified in the protocol (D10±3d, W4±3d, W13±7d, W26±14d, W52±14d/EOS/unscheduled) (excluding circumstances of force majeure) during the study period.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

1

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Hubei
      • Wuhan, Hubei, Cina, 430030
        • Union Hospital Tongji Medical College Huazhong University Of Science And Technology

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Bambino

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  • Subjects must meet all of the following inclusion criteria to be enrolled in the study:

    1. Age between 1 year and 17 years (inclusive) at the time of signing the ICF, male or female;
    2. Confirmed homozygous or compound heterozygous mutation in the OTOF gene as documented in a report issued by a qualified genetic testing institution;
    3. Audiometric testing (reports from within 6 months prior to signing the ICF are acceptable): Severe or profound deafness (Click ABR ≥ 80 dBnHL);
    4. Has received cochlear implantation and has reasonable expectations;
    5. Vital signs, physical examination, laboratory tests (complete blood count, blood biochemistry, coagulation function, urinalysis, etc.), and 12-lead ECG are all normal or show abnormalities judged by the investigator to be clinically insignificant;
    6. Subject and/or their legal guardian signs the informed consent form.

      Exclusion Criteria:

  • Subjects who meet any of the following criteria are not eligible for enrollment:

    1. Presence of other definite genetic mutations causing deafness other than the OTOF gene that may affect the judgment of the treatment effect of the OTOF investigational drug;
    2. History of severe allergic reactions to any drug or its components in this study;
    3. Prior gene therapy and/or oligonucleotide drug treatment in the ear that has undergone cochlear implantation;
    4. Blood AAV2 neutralizing antibody titer > 1:2000;
    5. Presence of systemic diseases or receipt of related treatments that may affect hearing or surgical procedures;
    6. Inability to undergo general anesthesia;
    7. History of major inner ear surgery (judged by the investigator as inappropriate for gene therapy);
    8. Other types of deafness unsuitable for otologic surgery, such as deafness caused by middle-inner ear developmental abnormalities or malformations, vestibulocochlear nerve abnormalities, conductive hearing loss, mixed hearing loss, or syndromic malformations as detected by CT/MRI;
    9. Otologic diseases that may interfere with the planned surgery or interpretation of study endpoints, such as acute-chronic otitis media, Meniere's disease, acoustic neuroma, sudden deafness with no hearing recovery, etc.;
    10. History of drug abuse, or receipt of any known ototoxic drug therapy within 6 months (e.g., aminoglycosides, cisplatin, loop diuretics, etc.), or receipt of antiviral and immunosuppressive therapy within 3 months, or vaccination within 1 month;
    11. Subjects currently receiving or likely to receive immunosuppressive therapy other than that required for this study;
    12. Allergy or intolerance to glucocorticoids;
    13. History of malignant tumors or meningitis;
    14. Presence of persistent or active infection; subjects who are HBsAg positive with peripheral blood HBV DNA titer above the lower limit of detection; subjects who are HCV antibody positive with peripheral blood HCV RNA titer above the lower limit of detection; subjects who are HIV antibody positive or have other immunodeficiency diseases; subjects with positive syphilis serology;
    15. Subjects of childbearing potential who refuse to use effective contraceptive measures (hormonal, barrier methods, or abstinence) from the time of signing the ICF through 12 months after AAV injection;
    16. Female subjects of childbearing potential with a positive serum pregnancy test, or who are currently pregnant or breastfeeding;
    17. Subjects who have participated in any other clinical study within 4 weeks prior to the first dose and have already received study drug or treatment (including drug and device clinical studies, excluding non-interventional studies);
    18. Unwilling or unable to comply with this study protocol;
    19. Subjects whom the investigator judges to have any medical condition that renders them unable to participate in this study or complete the subsequent follow-up.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: EA0010 Injection Arm

EA0010 is an investigational gene therapy product comprising two adeno-associated virus (AAV) vectors carrying OTOF gene sequences. The two components (Solution A and Solution B) are mixed at a 1:1 ratio immediately prior to administration.

Dose and Administration: Participants will receive a single dose of 2.0 × 10^11 viral genomes (vg) per ear. The total injection volume will range from 10 to 40 μL, adjusted based on the actual viral titer of the manufactured batch.

Administration: Single unilateral intratympanic injection via the stapes annular ligament.

Pre-medication: Systemic glucocorticoid therapy will be initiated 3 days prior to surgery (Day -3) to mitigate potential inflammation.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Incidence and severity of Adverse Events (AEs), Serious Adverse Events (SAEs), and Dose-Limiting Toxicities (DLTs) to Week 26
Lasso di tempo: Day 0 (injection) through Week 26
AEs, SAEs, and DLTs will be evaluated according to NCI-CTCAE v5.0. Safety evaluation includes: physical examination (including cranial nerve function), laboratory indicators (routine blood test, blood biochemistry, urinalysis, coagulation function), vital signs, ECG, peripheral blood neutralizing antibody testing, and peripheral blood AAV shedding testing.
Day 0 (injection) through Week 26

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Incidence and severity of AEs, SAEs, and DLTs of EA0010 injection to Week 52
Lasso di tempo: Week 27 through Week 52
AEs, SAEs, and DLTs will be evaluated according to NCI-CTCAE v5.0. Safety evaluation includes: physical examination (including cranial nerve function), laboratory indicators (routine blood test, blood biochemistry, urinalysis, coagulation function), vital signs, ECG, peripheral blood neutralizing antibody testing, and peripheral blood AAV shedding testing.
Week 27 through Week 52
Efficacy of EA0010 on hearing levels as measured by pure-tone or behavioral audiometry
Lasso di tempo: Baseline, Week 4, Week 13, Week 26, Week 52, and annually through Year 5
Efficacy of EA0010 on hearing recovery, assessed by PTA or age-appropriate behavioral audiometry.
Baseline, Week 4, Week 13, Week 26, Week 52, and annually through Year 5
Efficacy of EA0010 on auditory function as measured by ABR (Auditory Brainstem Response) testing
Lasso di tempo: Baseline, Day 10, Week 4, Week 13, Week 26, Week 52, and annually through Year 5
Objective electrophysiological assessment of auditory pathway response following EA0010 injection.
Baseline, Day 10, Week 4, Week 13, Week 26, Week 52, and annually through Year 5

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

23 maggio 2026

Completamento primario (Stimato)

31 maggio 2027

Completamento dello studio (Stimato)

31 luglio 2027

Date di iscrizione allo studio

Primo inviato

28 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

5 agosto 2026

Primo Inserito (Effettivo)

7 agosto 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

12 agosto 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

10 agosto 2026

Ultimo verificato

1 agosto 2026

Maggiori informazioni

Termini relativi a questo studio

Parole chiave

Altri numeri di identificazione dello studio

  • GSEA0011

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Descrizione del piano IPD

Individual participant data (IPD) will not be shared. The data generated in this study are proprietary. Aggregate safety and efficacy data will be reported in clinical study reports and potential publications.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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