A Phase II Study of SHR-2173 Injection in Patients With Myasthenia Gravis
A Phase II, Randomized, Double-Blind, Placebo-Controlled Clinical Trial to Evaluate the Efficacy and Safety of SHR-2173 in Patients With Generalized Myasthenia Gravis
Panoramica dello studio
Stato
Stato
Condizioni
Condizioni
Intervento / Trattamento
Intervento / Trattamento
Tipo di studio
Tipo di studio
Iscrizione (Stimato)
Iscrizione
Fase
Fase
- Fase 2
Contatti e Sedi
Contatto studio
Contatto studio
- Nome: Kunming Li
- Numero di telefono: 0518-82342973
- Email: kunming.li@hengrui.com
Luoghi di studio
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Hunan
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Changsha, Hunan, Cina, 410008
- Xiangya Hospital of Central South University
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Investigatore principale:
- Huan Yang
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Shanghai Municipality
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Shanghai, Shanghai Municipality, Cina, 200040
- Huashan Hospital, Fudan University
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Investigatore principale:
- Chongbo Zhao
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-
Criteri di partecipazione
Criteri di ammissibilità
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
Inclusion Criteria:
- Male and female participants aged 18-75 years, confirmed diagnosis of generalized myasthenia gravis (gMG) (Myasthenia Gravis Foundation of America [MGFA] class II-IV).
- Positive for anti-AChR antibody or anti-MuSK antibody.
- MG-ADL total score ≥5 at screening and baseline, with >50% of the score attributable to non-ocular items.
- QMG score ≥11 at screening and baseline.
- Maintenance on stable standard of care (SOC) therapy.
- No contraindication to at least one rescue therapy: IVIg or PLEX.
- Provided written informed consent (ICF) after full understanding of the study content, procedures, and potential adverse reactions.
- Female subjects with fertility or male participants whose partners are women of childbearing age must avoid donating sperm/eggs from the date of signing the ICF until 12 weeks after the last study medication, and agree to take contraceptive measures as specified in the protocol
Exclusion Criteria:
Presence of any of the following medical histories or comorbidities:
- Any untreated thymic epithelial tumor, mediastinal germ cell tumor, or other malignant mediastinal mass; or any thymic cyst or other mass requiring immediate intervention per investigator judgment;
- Previous history of thymic tumor not meeting protocol requirements;
- Myasthenic crisis (MGFA Class V) within 3 months prior to randomization;
- Any known disease other than gMG that may interfere with study procedures and assessments;
- A history of progressive multifocal leukoencephalopathy (PML);
- A history of body irradiation or organ transplantation.
Use of any of the following drugs/treatments or participation in a clinical study:
- Prior treatment with CAR-T or other cellular therapy, or T-cell engager (TCE) therapy;
- Anti-CD20 monoclonal antibody within 6 months prior to randomization; other B-cell or plasma cell-depleting therapy within 6-12 months prior to randomization;
- Alkylating agent within 12 weeks prior to randomization;
- Any biologic for MG treatment within 12 weeks prior to randomization;
- Neonatal Fc receptor antagonist therapy within 8 weeks prior to randomization;
- Janus kinase (JAK), Bruton tyrosine kinase (BTK), or tyrosine kinase 2 (TYK2) inhibitor within 12 weeks prior to randomization;
- IVIg, subcutaneous immunoglobulin, or PLEX therapy within 4 weeks prior to randomization;
- Live/attenuated live vaccine within 4 weeks prior to randomization, or planned vaccination during the study.
- A history of malignancy within 5 years prior to screening;
Infection-related medical history and examinations:
- A history of herpes zoster meeting any of the following: 1) A history of disseminated herpes zoster, herpes zoster encephalitis, or ocular herpes zoster involving the retina; 2) Recurrent herpes zoster with 2 or more episodes within 2 years; 3) Herpes zoster infection not fully resolved within 12 weeks prior to screening;
- A history of tuberculosis (TB) or latent TB infection;
- A known history of primary immunodeficiency, splenectomy, or any underlying condition predisposing to infection;
- A history of recurrent infections requiring hospitalization and intravenous antibiotics;
- Any infection requiring hospitalization and/or intravenous antimicrobial therapy within 8 weeks prior to randomization, or any infection requiring oral antimicrobial therapy within 2 weeks prior to randomization;
- Positive test result for hepatitis B surface antigen (HBsAg), hepatitis C virus antibody, treponemal pallidum antibody, or human immunodeficiency virus (HIV) antibody; for patients with HBsAg-negative but hepatitis B core antibody (HBcAb)-positive, regardless of the status of hepatitis B surface antibody (HBsAb), HBV-DNA testing is required to confirm their condition, with HBV-DNA-positive patients excluded and HBV-DNA-negative patients eligible to participate in the study.
General situation:
- Pregnant or lactating females;
- A history of alcohol abuse or illicit drug abuse within 1 year prior to screening;
- A history of allergic diathesis, or known hypersensitivity/intolerance to any component of the investigational product;
- Major surgery within 3 months prior to the screening, or planned major surgery during the study;
- Any condition that, in the investigator's judgment, may affect evaluation of study drug safety and efficacy, or any other condition that renders the subject ineligible.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Quadruplicare
Numero di armi
Armi e interventi
Gruppo di partecipanti / ArmGruppo di partecipanti / Arm |
Intervento / TrattamentoIntervento / Trattamento |
|---|---|
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Comparatore placebo: Placebo
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Placebo
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Sperimentale: Gruppo di trattamento A: iniezione di SHR-2173
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Iniezione SHR-2173; Dose elevata
Iniezione SHR-2173; Bassa dose
|
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Sperimentale: Gruppo di trattamento B: iniezione SHR-2173
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Iniezione SHR-2173; Dose elevata
Iniezione SHR-2173; Bassa dose
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
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Change from baseline in MG-ADL total score
Lasso di tempo: at Week 24
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at Week 24
|
Misure di risultato secondarie
Misure di risultato secondarie
Misura del risultato |
Lasso di tempo |
|---|---|
|
Change from baseline in Quantitative Myasthenia Gravis (QMG) score
Lasso di tempo: at Week 24
|
at Week 24
|
|
Change from baseline in Myasthenia Gravis Composite (MGC) total score
Lasso di tempo: at Week 24
|
at Week 24
|
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Change from baseline in MG-ADL domain scores (ocular, bulbar, respiratory, limb)
Lasso di tempo: at Week 24
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at Week 24
|
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Change from baseline in QMG domain scores (ocular, bulbar, respiratory, limb)
Lasso di tempo: at Week 24
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at Week 24
|
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Proportion of participants with ≥3-point reduction from baseline in MG-ADL total score
Lasso di tempo: at Week 24
|
at Week 24
|
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Proportion of participants with ≥50% reduction from baseline in MG-ADL total score
Lasso di tempo: at Week 24
|
at Week 24
|
|
Proportion of participants with ≥5-point reduction from baseline in QMG score
Lasso di tempo: at Week 24
|
at Week 24
|
|
Proportion of participants achieving Minimal Symptom Expression (MSE; MG-ADL total score 0 or 1) at Week 24
Lasso di tempo: at Week 24
|
at Week 24
|
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Change from baseline in Myasthenia Gravis Quality of Life 15-item revised (MG-QoL15r) total score
Lasso di tempo: at Week 24
|
at Week 24
|
|
Change from baseline in Neuro-QoL Fatigue subscale score
Lasso di tempo: at Week 24
|
at Week 24
|
|
Change from baseline in European Quality of Life 5-Dimensions 5-Levels (EQ-5D-5L) index score
Lasso di tempo: at Week 24
|
at Week 24
|
|
Proportion of participants without rescue therapy
Lasso di tempo: through Week 24
|
through Week 24
|
|
Incidence, severity grading, and drug-relatedness of adverse events (AEs)
Lasso di tempo: through Week 24
|
through Week 24
|
|
Incidence, severity grading, and drug-relatedness of serious adverse events (SAEs)
Lasso di tempo: through Week 24
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through Week 24
|
|
Incidence, severity grading, and drug-relatedness of adverse events of special interest (AESIs)
Lasso di tempo: through Week 24
|
through Week 24
|
|
Change from baseline in C-SSRS
Lasso di tempo: through Week 24
|
through Week 24
|
Collaboratori e investigatori
Sponsor
Sponsor
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Inizio studio
Completamento primario (Stimato)
Completamento primario
Completamento dello studio (Stimato)
Completamento dello studio
Date di iscrizione allo studio
Primo inviato
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Primo Inserito
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento pubblicato
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Malattie del sistema nervoso
- Neoplasie per sede
- Neoplasie
- Malattie neuromuscolari
- Malattie autoimmuni
- Malattie del sistema immunitario
- Malattie autoimmuni del sistema nervoso
- Malattie Neurodegenerative
- Sindromi Paraneoplastiche, Sistema Nervoso
- Neoplasie del sistema nervoso
- Sindromi paraneoplastiche
- Malattie della giunzione neuromuscolare
- Miastenia grave
Altri numeri di identificazione dello studio
Altri numeri di identificazione dello studio
- SHR-2173-206
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
Informazioni su farmaci e dispositivi, documenti di studio
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Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
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