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A Clinical Study to Evaluate the Safety and Efficacy of GT802 Injection in the Treatment of Refractory Generalized Myasthenia Gravis

4 novembre 2026 mis à jour par: Daishi Tian

This is a single-arm, open-label, dose-escalating clinical trial designed to evaluate the safety, efficacy and cellular pharmacokinetics of GT802 in the treatment of refractory generalized myasthenia gravis.

Aperçu de l'étude

Statut

Pas encore de recrutement

Intervention / Traitement

Description détaillée

The study includes 3 planned dose cohorts as follows: Dose 1: total of 8.5 mg, administered as 4 infusions at 1.0 mg, 1.5 mg, 3.0 mg, and 3.0 mg; Dose 2: total of 13.5 mg, administered as 4 infusions at 1.5 mg, 3.0 mg, 4.5 mg, and 4.5 mg; De-escalation dose: total of 4.5 mg, administered as 4 infusions at 0.5 mg, 1.0 mg, 1.5 mg, and 1.5 mg.

Each participant will receive treatment from one dose cohort. It is planned to enroll 4-12 participants in total, with the number of participants per dose cohort as follows: Dose 1: 1-6 participants; Dose 2: 3-6 participants; De-escalation dose: 0-6 participants.

Type d'étude

Interventionnel

Inscription (Estimé)

12

Phase

  • Première phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

    • Hubei
      • Wuhan, Hubei, Chine, 430000
        • Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology
        • Chercheur principal:
          • Daishi Tian
        • Chercheur principal:
          • Chuan Qin
        • Contact:

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 65 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Non

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • 1. The participant or their legally authorized representative voluntarily signs the written informed consent form and is willing and able to comply with the study procedures.

  • 2. Aged 18-65 years (inclusive) at the time of informed consent, without gender restriction.

  • 3. Expected survival > 12 weeks.

  • 4. Any prior systemic therapy for the indication must have a washout period of at least 4 weeks or 5 half-lives, whichever is shorter, before the participant is scheduled to receive study treatment.

  • 5. Toxicities attributable to prior treatment must have stabilized and recovered to Grade ≤1.

  • 6. Refractory generalized myasthenia gravis, as defined in the protocol.

  • 7. Screening laboratory results meet the criteria specified in the protocol.

  • 8. Pregnancy requirements:

    1. At screening, serum beta human chorionic gonadotropin (β-hCG) pregnancy test is negative as confirmed by the investigator.
    2. Agrees to refrain from breastfeeding during study participation until at least 1 year after infusion of GT802 Injection or until GT802 cells are no longer detectable by 2 consecutive flow cytometry assays, whichever occurs later.
    3. Male participants with female partners and female participants of childbearing potential agree to use highly effective contraception (e.g., oral contraceptives, intrauterine device or condoms) starting at screening and continuing until at least 1 year after infusion of GT802 Injection or until GT802 cells are no longer detectable by 2 consecutive flow cytometry assays, whichever occurs later. Male participants must agree to use condoms during sexual contact with pregnant females or females of childbearing potential for at least 1 year after GT802 Injection infusion, even after successful vasectomy.

Exclusion Criteria:

  • 1. Contraindication or hypersensitivity to any component of the investigational product.
  • 2. Presence of conditions specified in the protocol within 6 months prior to signing the informed consent form.[沈9.1]
  • 3. History of active malignancy or any malignancy within 5 years prior to screening.
  • 4. Presence of any active or untreated thymoma, or history of thymic carcinoma or other early pseudotumors of thymic malignancy.
  • 5. Autoimmune diseases other than the study disease that require systemic glucocorticoids or immunosuppressants.
  • 6. Requirement for long-term administration of medications affecting coagulation function.
  • 7. Participants with clinically obvious bleeding symptoms or definite bleeding tendency within 6 months before screening.
  • 8. Presence of severe underlying medical conditions at screening.
  • 9. Positive result for any of the following tests: a) Positive human immunodeficiency virus (HIV) antibody; b) Positive hepatitis B surface antigen (HBsAg) and/or positive hepatitis B core antibody (HBcAb), with HBV-DNA above the lower limit of quantitation of the assay; c) Positive hepatitis C virus (HCV) antibody, with HCV-RNA above the lower limit of quantitation of the assay; d) Positive syphilis antibody (excluding false-positive results caused by underlying diseases).
  • 10. Positive cytomegalovirus (CMV)-DNA and Epstein Barr virus (EBV)-DNA in peripheral blood.
  • 11. Active tuberculosis prior to screening.
  • 12. Received any other investigational medicinal product within 4 weeks before signing the informed consent form (ICF).
  • 13. Received intravenous immunoglobulin, plasma exchange or immunoadsorption therapy within 4 weeks prior to study treatment.
  • 14. Received B-cell targeted therapy within 1 month prior to study treatment.
  • 15. Received tacrolimus, cyclosporine, azathioprine, mycophenolate mofetil, mycophenolic acid, methotrexate, etc., within 2 weeks prior to study treatment.
  • 16. Received neonatal Fc receptor (FcRn) antagonist therapy within 2 weeks prior to study treatment.
  • 17. Received complement inhibition therapy within 2 weeks prior to study treatment.
  • 18. Received systemic glucocorticoids at a dose >10 mg/day prednisone equivalent within 7 days prior to study treatment.
  • 19. Received live attenuated vaccines or mRNA vaccines within 8 weeks before enrollment, or inactivated vaccines within 4 weeks before enrollment.
  • 20. Underwent major surgery within 8 weeks before screening, or planned to undergo surgery during the study period.
  • 21. History of organ transplantation, splenectomy, allogeneic or autologous stem cell transplantation.
  • 22. Presence of non-removable, clinically significant long-term indwelling catheters or drainage devices.
  • 23. Uncontrolled large-volume serous cavity effusion despite treatment.
  • 24. Prior receipt of CAR-T products targeting any antigen or other gene-edited cell biotherapies.
  • 25. The investigator judges that any condition exists that would prevent the participant from completing the entire trial, confound the trial results, or make trial participation not in the participant's best interest.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: N / A
  • Modèle interventionnel: Affectation à un seul groupe
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: GT802 Injection treatment group

Participants with MG administered GT802 Injection

Injection

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Adverse Events (AEs) occurring after infusion and their proportions
Délai: From infusion to at least 1 year

Adverse Events (AEs) occurring after infusion and their proportions

From infusion to at least 1 year

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Quantitative Myasthenia Gravis (QMG) score
Délai: From infusion to 12 months

To assess the preliminary efficacy of GT802 Injection in participants with refractory generalized myasthenia gravis per QMG score.

From infusion to 12 months
Myasthenia Gravis Activities of Daily Living (MG-ADL) score
Délai: From infusion to 12 months

To assess the preliminary efficacy of GT802 Injection in participants with refractory generalized myasthenia gravis per MG-ADL score.

From infusion to 12 months
Time to maximum amplification (Tmax)
Délai: From infusion to 12 months

Time to maximum amplification (Tmax) of cells following GT802 infusion

From infusion to 12 months
Maximum amplification (Cmax)
Délai: From infusion to 12 months

The maximum observed concentration of the circulating GT802 CAR-T cells

From infusion to 12 months
Area under the curve (AUC)
Délai: From infusion to 12 months

Area under the curve (AUC) of cellular expansion following GT802 infusion

From infusion to 12 months
Duration of Detectable Concentration (Tlast)
Délai: From infusion to 12 months

Duration of Detectable Concentration (Tlast) refers to the time period from the infusion of GT802 cells to the last time point at which the target cells can be detected in the peripheral blood or target tissues.

From infusion to 12 months
Chimeric Antigen Receptor T cell (CAR-T)-associated serum cytokines
Délai: From infusion to 2 months

Monitor serum cytokine levels after infusion

From infusion to 2 months
Anti-drug antibodies (ADA) Response to GT802 Measured by Immunoassay.
Délai: From infusion to 12 months

Changes in anti-drug antibodies (ADA) before and after treatment. Serum anti-drug antibody (ADA) response to GT802, including anti-CAR and anti-PEG antibodies, measured by immunoassay. Samples collected at pre-screening (PEG only), Day 14, Day 28, Month 3, Month 6, and Month 12 post-first infusion. Positive results trigger titer confirmation and continued monitoring until negative or below lower limit of detection.

From infusion to 12 months

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Les enquêteurs

  • Chercheur principal: Chuan Qin, Tongji Hospital
  • Chercheur principal: Daishi Tian, Tongji Hospital

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 décembre 2026

Achèvement primaire (Estimé)

30 décembre 2031

Achèvement de l'étude (Estimé)

30 décembre 2031

Dates d'inscription aux études

Première soumission

27 octobre 2026

Première soumission répondant aux critères de contrôle qualité

4 novembre 2026

Première publication (Réel)

5 novembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

5 novembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

4 novembre 2026

Dernière vérification

1 novembre 2026

Plus d'information

Termes liés à cette étude

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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