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Safety, Tolerability, and Preliminary Antitumor Activity of Cationic Peptide-IL22BP mRNA in Advanced Solid Tumors

12 de julho de 2026 atualizado por: Xingchen Peng, West China Hospital

A Clinical Trial of Cationic Peptide-IL22BP mRNA for Safety, Tolerability, and Preliminary Antitumor Activity in Patients With Advanced Malignant Solid Tumors

The goal of this phase 1 clinical trial is to evaluate the safety, tolerability, and preliminary antitumor activity of a peptide-delivered IL-22BP biotherapy in patients with advanced solid tumors. The main questions it aims to answer are:

Is the IL-22BP formulation safe and tolerable? Does the IL-22BP formulation show preliminary antitumor activity?

Visão geral do estudo

Descrição detalhada

This is a phase 1, single-arm, open-label, dose-escalation clinical trial designed to evaluate a peptide-based IL-22BP mRNA gene therapy in patients with refractory advanced malignant solid tumors. The investigational product uses a peptide delivery platform composed of natural amino acids, which is intended to improve biocompatibility, reduce toxicity, simplify manufacturing, and avoid key patent limitations associated with conventional lipid nanoparticle (LNP) systems. Unlike a traditional tumor vaccine, this intervention is designed as a targeted gene therapy that promotes intratumoral expression of IL-22BP protein to inhibit tumor progression. Preclinical toxicology studies of the peptide-mRNA complex have shown an acceptable safety profile, with no notable abnormalities in hematological or biochemical parameters. The study will use a standard "3+3" dose-escalation design to assess three fixed mRNA dose levels. The primary objective is to characterize the safety and tolerability of the IL-22BP gene formulation, and the secondary objective is to evaluate its preliminary antitumor activity.

Tipo de estudo

Intervencional

Inscrição (Estimado)

18

Estágio

  • Fase 1

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.

Contato de estudo

  • Nome: Xingchen PXC Peng, Ph.D.
  • Número de telefone: 86+13108175138
  • E-mail: 13108175138@163.com

Locais de estudo

    • Sichuan
      • Chengdu, Sichuan, China, 610041
        • Recrutamento
        • West China Hospital of Sichuan University
        • Contato:

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:

  • Male or female patients aged ≥18 years and ≤70 years.
  • Histopathologically confirmed advanced recurrent/metastatic malignant solid tumors that are refractory to second-line treatment and have no available standard clinical therapeutic options (e.g., advanced soft tissue sarcoma, advanced head and neck squamous cell carcinoma, malignant melanoma, etc.).
  • Eastern Cooperative Oncology Group (ECOG) performance status score of 0-1.
  • Expected overall survival ≥3 months.
  • Interval from the last chemotherapy, radiotherapy, or surgery ≥28 days.
  • Interval from the last use of nitrosourea or mitomycin C ≥6 weeks.
  • Adequate organ function, defined by the following laboratory parameters within 14 days prior to enrollment:
  • Hemoglobin ≥90 g/L (no blood transfusion within 14 days).
  • Absolute neutrophil count >1.5 × 10⁹/L.
  • Platelet count ≥80 × 10⁹/L.
  • Total bilirubin ≤1.5 × upper limit of normal (ULN).
  • Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≤2.5 × ULN (≤5 × -ULN in case of liver metastasis).
  • Creatinine clearance ≥60 mL/min (calculated by Cockcroft-Gault formula).
  • Left ventricular ejection fraction (LVEF) ≥50%.
  • Signed written informed consent.

Exclusion Criteria:

  • Participation in another investigational drug clinical trial within 4 weeks.
  • Tumor located adjacent to major blood vessels or trachea.
  • Uncontrolled cardiac clinical symptoms or diseases, including New York Heart Association (NYHA) Class ≥2 heart failure, unstable angina, myocardial infarction within 1 year, or clinically significant supraventricular/ventricular arrhythmias requiring treatment or intervention.
  • Female patients who are pregnant or lactating.
  • Active pulmonary tuberculosis, bacterial or fungal infection (≥Grade 2 per NCI-CTCAE version 5.0), active human immunodeficiency virus (HIV) infection, active hepatitis B virus (HBV) infection, or hepatitis C virus (HCV) infection.
  • History of uncontrollable psychoactive substance abuse or presence of mental disorders.
  • Any active autoimmune disease or history of autoimmune disease, including but not limited to uveitis, enteritis, hypophysitis, nephritis, hyperthyroidism, and hypothyroidism.
  • Subjects with vitiligo or childhood asthma in complete remission (no adult intervention required) are eligible; subjects with asthma requiring bronchodilator therapy are excluded.
  • Receiving immunosuppressive therapy.
  • History of drug abuse or known medical, psychological, or social conditions that interfere with study compliance (e.g., alcoholism or illicit drug addiction).
  • Known hypersensitivity, allergy, or intolerance to the study drug CPIL22BP mRNA (including any excipients), or history of severe allergic reactions to any drugs, foods, or vaccines (e.g., anaphylactic shock, allergic laryngeal edema, allergic dyspnea, allergic purpura, thrombocytopenic purpura, local Arthus reaction, etc.).
  • Female subjects planning pregnancy, or male subjects whose partner plans pregnancy, from screening until 12 months after the last study drug injection.
  • Any concomitant disease that, in the investigator's judgment, may seriously compromise patient safety or prevent the subject from completing 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: Não randomizado
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Intratumoral CP-IL22BP mRNA injection group
CP-IL22BP mRNA will be administered via intratumoral injection. A total of 5 doses will be given, with subsequent doses administered once weekly after the first injection.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Number of Participants Experiencing Dose-Limiting Toxicities (DLTs)
Prazo: From the first dose to the end of treatment at 9 weeks
DLT is defined as any Treatment-Related Adverse Event (TRAE) or clinically significant laboratory abnormality occurring during the DLT observation period. TRAEs include events judged by the investigator to be "definitely," "probably," or "possibly" related to the study treatment. Severity will be graded according to NCI-CTCAE v5.0.
From the first dose to the end of treatment at 9 weeks
Number of participants with treatment discontinuation due to treatment-related adverse events during the first treatment cycle
Prazo: From the first dose to the end of treatment at 9 weeks
Treatment-related adverse events (TRAEs) will be assessed and graded according to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0. Treatment discontinuation is defined as permanent cessation of CP-IL22BP mRNA administration due to investigator-determined TRAEs occurring during the first treatment cycle.
From the first dose to the end of treatment at 9 weeks

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Progression-Free Survival
Prazo: Up to 6 months from the date of the first dose.
Progression-Free Survival (PFS) is defined as the time interval from the start of treatment until the first documented occurrence of disease progression (PD) according to RECIST v1.1, or death due to any cause, whichever occurs first.
Up to 6 months from the date of the first dose.
Overall Survival
Prazo: Up to 12 months from the date of the first dose.
OS is defined as the time interval from the start of treatment to death due to any cause. For participants who are still alive at the end of the study, data will be censored at the last known date of follow-up.
Up to 12 months from the date of the first dose.
Objective Response
Prazo: Time Frame: Up to 6 months from the date of the first dose.
Number of participants achieving a Best Overall Response (BOR) of either Complete Response (CR) or Partial Response (PR) according to RECIST v1.1. Due to the small sample size, data will be reported as absolute counts.
Time Frame: Up to 6 months from the date of the first dose.

Colaboradores e Investigadores

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

Patrocinador

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)

13 de julho de 2026

Conclusão Primária (Estimado)

30 de junho de 2027

Conclusão do estudo (Estimado)

30 de dezembro de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

30 de abril de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

6 de maio de 2026

Primeira postagem (Real)

13 de maio de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

14 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

12 de julho de 2026

Última verificação

1 de maio de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • 2026-520

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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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