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

12 luglio 2026 aggiornato da: 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?

Panoramica dello studio

Descrizione dettagliata

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 di studio

Interventistico

Iscrizione (Stimato)

18

Fase

  • Fase 1

Contatti e Sedi

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

Contatto studio

Luoghi di studio

    • Sichuan
      • Chengdu, Sichuan, Cina, 610041
        • Reclutamento
        • West China Hospital of Sichuan University
        • Contatto:

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:

  • 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.

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: Non randomizzato
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Number of Participants Experiencing Dose-Limiting Toxicities (DLTs)
Lasso di tempo: 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
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Progression-Free Survival
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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.

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)

13 luglio 2026

Completamento primario (Stimato)

30 giugno 2027

Completamento dello studio (Stimato)

30 dicembre 2027

Date di iscrizione allo studio

Primo inviato

30 aprile 2026

Primo inviato che soddisfa i criteri di controllo qualità

6 maggio 2026

Primo Inserito (Effettivo)

13 maggio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

14 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

12 luglio 2026

Ultimo verificato

1 maggio 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 2026-520

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

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 .

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