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
Studie Overzicht
Toestand
Toestand
Conditie
Conditie
Interventie / Behandeling
Interventie / Behandeling
Studietype
Studietype
Inschrijving (Geschat)
Inschrijving
Fase
Fase
- Fase 2
Contacten en locaties
Studiecontact
Studiecontact
- Naam: Kunming Li
- Telefoonnummer: 0518-82342973
- E-mail: kunming.li@hengrui.com
Studie Locaties
-
-
Hunan
-
Changsha, Hunan, China, 410008
- Xiangya Hospital of Central South University
-
Hoofdonderzoeker:
- Huan Yang
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, China, 200040
- Huashan Hospital, Fudan University
-
Hoofdonderzoeker:
- Chongbo Zhao
-
-
Deelname Criteria
Geschiktheidscriteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Beschrijving
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.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Verviervoudigen
Aantal wapens
Wapens en interventies
Deelnemersgroep / ArmDeelnemersgroep / Arm |
Interventie / BehandelingInterventie / Behandeling |
|---|---|
|
Placebo-vergelijker: Placebo
|
Placebo
|
|
Experimenteel: Behandelgroep A: SHR-2173-injectie
|
SHR-2173-injectie; Hoge dosis
SHR-2173-injectie; Lage dosis
|
|
Experimenteel: Behandelingsgroep B: SHR-2173 injectie
|
SHR-2173-injectie; Hoge dosis
SHR-2173-injectie; Lage dosis
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Change from baseline in MG-ADL total score
Tijdsspanne: at Week 24
|
at Week 24
|
Secundaire uitkomstmaten
Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Change from baseline in Quantitative Myasthenia Gravis (QMG) score
Tijdsspanne: at Week 24
|
at Week 24
|
|
Change from baseline in Myasthenia Gravis Composite (MGC) total score
Tijdsspanne: at Week 24
|
at Week 24
|
|
Change from baseline in MG-ADL domain scores (ocular, bulbar, respiratory, limb)
Tijdsspanne: at Week 24
|
at Week 24
|
|
Change from baseline in QMG domain scores (ocular, bulbar, respiratory, limb)
Tijdsspanne: at Week 24
|
at Week 24
|
|
Proportion of participants with ≥3-point reduction from baseline in MG-ADL total score
Tijdsspanne: at Week 24
|
at Week 24
|
|
Proportion of participants with ≥50% reduction from baseline in MG-ADL total score
Tijdsspanne: at Week 24
|
at Week 24
|
|
Proportion of participants with ≥5-point reduction from baseline in QMG score
Tijdsspanne: at Week 24
|
at Week 24
|
|
Proportion of participants achieving Minimal Symptom Expression (MSE; MG-ADL total score 0 or 1) at Week 24
Tijdsspanne: at Week 24
|
at Week 24
|
|
Change from baseline in Myasthenia Gravis Quality of Life 15-item revised (MG-QoL15r) total score
Tijdsspanne: at Week 24
|
at Week 24
|
|
Change from baseline in Neuro-QoL Fatigue subscale score
Tijdsspanne: at Week 24
|
at Week 24
|
|
Change from baseline in European Quality of Life 5-Dimensions 5-Levels (EQ-5D-5L) index score
Tijdsspanne: at Week 24
|
at Week 24
|
|
Proportion of participants without rescue therapy
Tijdsspanne: through Week 24
|
through Week 24
|
|
Incidence, severity grading, and drug-relatedness of adverse events (AEs)
Tijdsspanne: through Week 24
|
through Week 24
|
|
Incidence, severity grading, and drug-relatedness of serious adverse events (SAEs)
Tijdsspanne: through Week 24
|
through Week 24
|
|
Incidence, severity grading, and drug-relatedness of adverse events of special interest (AESIs)
Tijdsspanne: through Week 24
|
through Week 24
|
|
Change from baseline in C-SSRS
Tijdsspanne: through Week 24
|
through Week 24
|
Medewerkers en onderzoekers
Sponsor
Sponsor
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Studie start
Primaire voltooiing (Geschat)
Primaire voltooiing
Studie voltooiing (Geschat)
Studie voltooiing
Studieregistratiedata
Eerst ingediend
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Eerst geplaatst
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update geplaatst
Laatste update ingediend die voldeed aan QC-criteria
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
- Ziekten van het zenuwstelsel
- Neoplasmata per site
- Neoplasmata
- Neuromusculaire aandoeningen
- Auto-immuunziekten
- Ziekten van het immuunsysteem
- Auto-immuunziekten van het zenuwstelsel
- Neurodegeneratieve ziekten
- Paraneoplastische syndromen, zenuwstelsel
- Neoplasmata van het zenuwstelsel
- Paraneoplastische syndromen
- Neuromusculaire junctieziekten
- Myasthenia Gravis
Andere studie-ID-nummers
Andere studie-ID-nummers
- SHR-2173-206
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .