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Telitacicept for Refractory Chronic Inflammatory Demyelinating Polyneuropathy

13 maggio 2026 aggiornato da: 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.

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

76

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

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

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore attivo: 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.
Altri nomi:
  • Corticosteroidi
  • Immunoglobulina endovenosa
  • Immunosuppressive agents
Sperimentale: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Percentage of Participants With Confirmed Evidence of Clinical Improvement
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Incidence of Adverse Events
Lasso di tempo: 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
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

26 settembre 2025

Completamento primario (Stimato)

31 agosto 2027

Completamento dello studio (Stimato)

31 agosto 2027

Date di iscrizione allo studio

Primo inviato

17 novembre 2025

Primo inviato che soddisfa i criteri di controllo qualità

13 maggio 2026

Primo Inserito (Effettivo)

19 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

19 maggio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

13 maggio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Prove cliniche su Conventional Therapy

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