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Telitacicept for Refractory Chronic Inflammatory Demyelinating Polyneuropathy

13 de maio de 2026 atualizado por: Cunjin Zhang, Sichuan Academy of Medical Sciences

Study on the Efficacy and Safety of Telitacicept in Refractory Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

This multicenter, randomized, controlled trial aims to evaluate the efficacy and safety of Telitacicept in patients with refractory chronic inflammatory demyelinating polyneuropathy (CIDP). Eligible patients will be randomly assigned to receive either conventional therapy alone or Telitacicept plus conventional therapy for 24 weeks. Efficacy will be assessed using CIDP-related clinical and functional measures, including the Inflammatory Neuropathy Cause and Treatment (INCAT) disability score, Inflammatory Rasch-built Overall Disability Scale (I-RODS), Medical Research Council (MRC) sum score, grip strength, and the Timed Up and Go (TUG) test. Safety will be evaluated by monitoring adverse events, including their onset, duration, clinical manifestations, and management.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Estimado)

76

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

    • Sichuan
      • Chengdu, Sichuan, China, 610072
        • Sichuan Provincial People's Hospital

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Inclusion Criteria: (1) Male or female participants aged 18 to 65 years, inclusive.

(2) Diagnosis of refractory chronic inflammatory demyelinating polyneuropathy (CIDP). Refractory CIDP is defined as the absence of evidence of clinical improvement (ECI) after at least 1 month of at least one first-line therapy, including intravenous immunoglobulin, corticosteroids, or plasma exchange, or a persistently elevated INCAT disability score of ≥2. ECI is defined as meeting at least one of the following criteria: a. A decrease of ≥1 point in the adjusted INCAT disability score; b. An increase of ≥4 points in the I-RODS total score; c. An increase of ≥3 points in the MRC sum score; d. An improvement of ≥8 kPa in grip strength. (3) INCAT disability score of 2 to 9. (4) Able to fully understand the study, willing to comply with study procedures, and able to provide written informed consent.

Exclusion Criteria:

  1. Progressive neurological disease unrelated to CIDP.
  2. Limb numbness or weakness caused by other etiologies, including but not limited to hereditary demyelinating neuropathy, neuropathy secondary to infection or systemic disease, diabetic neuropathy, drug- or toxin-induced neuropathy, multifocal motor neuropathy, polyneuropathy associated with IgM monoclonal gammopathy, POEMS syndrome, cerebral infarction, acute myelitis, multiple sclerosis, neuromyelitis optica spectrum disorder, or other conditions that may cause limb numbness or muscle weakness.
  3. Active hepatitis or severe hepatic dysfunction, defined as liver function test values greater than two times the upper limit of normal. Participants who are positive for hepatitis B surface antigen (HBsAg) will be excluded. Participants who are positive only for hepatitis B core antibody (HBc-Ab) must undergo quantitative HBV-DNA testing and will not be excluded if the result is negative.
  4. Severe renal impairment, including acute kidney injury or chronic kidney disease, or serum creatinine clearance <60 mL/min calculated using the Cockcroft-Gault equation.
  5. Current pregnancy, breastfeeding, or planned pregnancy within 48 weeks.
  6. Participation in another interventional clinical trial within 28 days before enrollment or within five half-lives of the investigational drug, whichever is longer.
  7. History of splenectomy.
  8. History of allergic reactions to contrast agents or intravenously administered human-derived biological products.
  9. Severe psychiatric symptoms that preclude cooperation with study procedures.
  10. Treatment with B-cell-depleting agents, such as rituximab, within 6 months before enrollment, or failure of B-cell counts to recover to the normal range, whichever is longer.
  11. Active tuberculosis.
  12. Diabetes mellitus.
  13. Failure to complete serum ganglioside antibody testing to exclude other diseases.
  14. Any other condition that, in the investigator's judgment, makes the participant unsuitable for the study.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador Ativo: Conventional Therapy Group
Participants in this group will receive conventional therapy, including intravenous immunoglobulin or corticosteroids, with immunosuppressive agents permitted when clinically indicated.
Conventional therapy may include intravenous immunoglobulin or corticosteroids, with immunosuppressive agents permitted when clinically indicated.
Outros nomes:
  • Corticosteróides
  • Imunoglobulina intravenosa
  • Immunosuppressive agents
Experimental: Telitacicept Plus Conventional Therapy Group
Participants in this group will receive Telitacicept in addition to conventional therapy for 24 weeks. Conventional therapy may include intravenous immunoglobulin or corticosteroids, with immunosuppressive agents permitted when clinically indicated.
Telitacicept will be administered by subcutaneous injection in addition to conventional therapy for 24 weeks.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Percentage of Participants With Confirmed Evidence of Clinical Improvement
Prazo: Baseline, Week 2, Week 4, Week 8, Week 16, and Week 24
Percentage of participants with confirmed evidence of clinical improvement, defined according to prespecified improvements in CIDP-related clinical and functional assessments.
Baseline, Week 2, Week 4, Week 8, Week 16, and Week 24
Change From Baseline in Adjusted INCAT Disability Score
Prazo: Baseline, Week 2, Week 4, Week 8, Week 16, and Week 24
Change from baseline in the adjusted Inflammatory Neuropathy Cause and Treatment disability score.
Baseline, Week 2, Week 4, Week 8, Week 16, and Week 24
Change From Baseline in MRC Sum Score
Prazo: Baseline, Week 2, Week 4, Week 8, Week 16, and Week 24
Change from baseline in the Medical Research Council sum score.
Baseline, Week 2, Week 4, Week 8, Week 16, and Week 24
Change From Baseline in I-RODS Score
Prazo: Baseline, Week 2, Week 4, Week 8, Week 16, and Week 24
Change from baseline in the Inflammatory Rasch-built Overall Disability Scale score.
Baseline, Week 2, Week 4, Week 8, Week 16, and Week 24
Change From Baseline in Timed Up and Go Test
Prazo: Baseline, Week 2, Week 4, Week 8, Week 16, and Week 24
Change from baseline in the Timed Up and Go test.
Baseline, Week 2, Week 4, Week 8, Week 16, and Week 24
Change From Baseline in Mean Grip Strength
Prazo: Baseline, Week 2, Week 4, Week 8, Week 16, and Week 24
Change from baseline in mean grip strength.
Baseline, Week 2, Week 4, Week 8, Week 16, and Week 24

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Incidence of Adverse Events
Prazo: Baseline, Week 2, Week 4, Week 8, Week 16, and Week 24
Incidence of adverse events during the study period, including the time of onset, duration, clinical manifestations, severity, relationship to study treatment, and actions taken.
Baseline, Week 2, Week 4, Week 8, Week 16, and Week 24
Change From Baseline in Serum IgG Levels
Prazo: Baseline, Week 2, Week 4, Week 8, Week 16, and Week 24
Change from baseline in serum immunoglobulin G levels during the study period.
Baseline, Week 2, Week 4, Week 8, Week 16, and Week 24

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

26 de setembro de 2025

Conclusão Primária (Estimado)

31 de agosto de 2027

Conclusão do estudo (Estimado)

31 de agosto de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

17 de novembro de 2025

Enviado pela primeira vez que atendeu aos critérios de CQ

13 de maio de 2026

Primeira postagem (Real)

19 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

19 de maio de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

13 de maio de 2026

Última verificação

1 de maio de 2026

Mais Informações

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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