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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

This study is a multicenter, randomized, double-blind, placebo-controlled Phase II clinical trial designed to evaluate the efficacy, safety, pharmacokinetics, and pharmacodynamics of SHR-2173 compared to placebo as an add-on therapy to standard of care (SOC) for the treatment of generalized myasthenia gravis (gMG). The study consists of a 4-week screening period, a 24-week treatment period, and a 12-week safety follow-up period.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

60

Fase

  • Fase 2

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

    • Hunan
      • Changsha, Hunan, Kina, 410008
        • Xiangya Hospital of Central South University
        • Ledende efterforsker:
          • Huan Yang
    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, Kina, 200040
        • Huashan Hospital, Fudan University
        • Ledende efterforsker:
          • Chongbo Zhao

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  1. Male and female participants aged 18-75 years, confirmed diagnosis of generalized myasthenia gravis (gMG) (Myasthenia Gravis Foundation of America [MGFA] class II-IV).
  2. Positive for anti-AChR antibody or anti-MuSK antibody.
  3. MG-ADL total score ≥5 at screening and baseline, with >50% of the score attributable to non-ocular items.
  4. QMG score ≥11 at screening and baseline.
  5. Maintenance on stable standard of care (SOC) therapy.
  6. No contraindication to at least one rescue therapy: IVIg or PLEX.
  7. Provided written informed consent (ICF) after full understanding of the study content, procedures, and potential adverse reactions.
  8. 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:

  1. Presence of any of the following medical histories or comorbidities:

    1. 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;
    2. Previous history of thymic tumor not meeting protocol requirements;
    3. Myasthenic crisis (MGFA Class V) within 3 months prior to randomization;
    4. Any known disease other than gMG that may interfere with study procedures and assessments;
    5. A history of progressive multifocal leukoencephalopathy (PML);
    6. A history of body irradiation or organ transplantation.
  2. Use of any of the following drugs/treatments or participation in a clinical study:

    1. Prior treatment with CAR-T or other cellular therapy, or T-cell engager (TCE) therapy;
    2. 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;
    3. Alkylating agent within 12 weeks prior to randomization;
    4. Any biologic for MG treatment within 12 weeks prior to randomization;
    5. Neonatal Fc receptor antagonist therapy within 8 weeks prior to randomization;
    6. Janus kinase (JAK), Bruton tyrosine kinase (BTK), or tyrosine kinase 2 (TYK2) inhibitor within 12 weeks prior to randomization;
    7. IVIg, subcutaneous immunoglobulin, or PLEX therapy within 4 weeks prior to randomization;
    8. Live/attenuated live vaccine within 4 weeks prior to randomization, or planned vaccination during the study.
  3. A history of malignancy within 5 years prior to screening;
  4. Infection-related medical history and examinations:

    1. 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;
    2. A history of tuberculosis (TB) or latent TB infection;
    3. A known history of primary immunodeficiency, splenectomy, or any underlying condition predisposing to infection;
    4. A history of recurrent infections requiring hospitalization and intravenous antibiotics;
    5. 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;
    6. 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.
  5. General situation:

    1. Pregnant or lactating females;
    2. A history of alcohol abuse or illicit drug abuse within 1 year prior to screening;
    3. A history of allergic diathesis, or known hypersensitivity/intolerance to any component of the investigational product;
    4. Major surgery within 3 months prior to the screening, or planned major surgery during the study;
    5. 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.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Placebo komparator: Placebo
Placebo
Eksperimentel: Behandlingsgruppe A: SHR-2173-injektion
SHR-2173-injektion; høj dosis
SHR-2173-injektion; Lav dosis
Eksperimentel: Behandlingsgruppe B: SHR-2173-injektion
SHR-2173-injektion; høj dosis
SHR-2173-injektion; Lav dosis

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Change from baseline in MG-ADL total score
Tidsramme: at Week 24
at Week 24

Sekundære resultatmål

Resultatmål
Tidsramme
Change from baseline in Quantitative Myasthenia Gravis (QMG) score
Tidsramme: at Week 24
at Week 24
Change from baseline in Myasthenia Gravis Composite (MGC) total score
Tidsramme: at Week 24
at Week 24
Change from baseline in MG-ADL domain scores (ocular, bulbar, respiratory, limb)
Tidsramme: at Week 24
at Week 24
Change from baseline in QMG domain scores (ocular, bulbar, respiratory, limb)
Tidsramme: at Week 24
at Week 24
Proportion of participants with ≥3-point reduction from baseline in MG-ADL total score
Tidsramme: at Week 24
at Week 24
Proportion of participants with ≥50% reduction from baseline in MG-ADL total score
Tidsramme: at Week 24
at Week 24
Proportion of participants with ≥5-point reduction from baseline in QMG score
Tidsramme: at Week 24
at Week 24
Proportion of participants achieving Minimal Symptom Expression (MSE; MG-ADL total score 0 or 1) at Week 24
Tidsramme: at Week 24
at Week 24
Change from baseline in Myasthenia Gravis Quality of Life 15-item revised (MG-QoL15r) total score
Tidsramme: at Week 24
at Week 24
Change from baseline in Neuro-QoL Fatigue subscale score
Tidsramme: at Week 24
at Week 24
Change from baseline in European Quality of Life 5-Dimensions 5-Levels (EQ-5D-5L) index score
Tidsramme: at Week 24
at Week 24
Proportion of participants without rescue therapy
Tidsramme: through Week 24
through Week 24
Incidence, severity grading, and drug-relatedness of adverse events (AEs)
Tidsramme: through Week 24
through Week 24
Incidence, severity grading, and drug-relatedness of serious adverse events (SAEs)
Tidsramme: through Week 24
through Week 24
Incidence, severity grading, and drug-relatedness of adverse events of special interest (AESIs)
Tidsramme: through Week 24
through Week 24
Change from baseline in C-SSRS
Tidsramme: through Week 24
through Week 24

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

1. juni 2026

Primær færdiggørelse (Anslået)

1. september 2027

Studieafslutning (Anslået)

1. december 2027

Datoer for studieregistrering

Først indsendt

20. maj 2026

Først indsendt, der opfyldte QC-kriterier

27. maj 2026

Først opslået (Faktiske)

3. juni 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

3. juni 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

27. maj 2026

Sidst verificeret

1. maj 2026

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

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UBESLUTET

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Kliniske forsøg med Generaliseret myasthenia gravis

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