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Phase I/II Trial of Electroporation-Delivered pBI-4 Vaccine (TriGrid™ PVX4) for Treatment of Women With HPV16-Positive CIN1 or Persistent Infection

10 de setembro de 2026 atualizado por: Chao, Angel, Chang Gung Memorial Hospital

A Randomized, Double-Blind, Placebo-Controlled Phase II Trial of pBI-4 Plasmid Administered Via Intramuscular TriGrid™ Electroporation Delivery System for Treatment of Women With HPV16-Positive Grade 1 Cervical Intraepithelial Neoplasia or Persistent HPV16 Infection

The purpose of this study is to evaluate the safety, efficacy, and tolerability of pBI-4, an investigational therapeutic DNA vaccine, in treating adult women with Human Papillomavirus type 16 (HPV16)-positive Grade 1 cervical intraepithelial neoplasia (CIN1) or persistent HPV16 infection.

This is a randomized, double-blind, placebo-controlled, multicenter Phase II trial in Taiwan, aiming to enroll a total of 94 female participants. Participants will be randomly assigned (1:1 ratio) to receive either a single 1.0 mg dose of the pBI-4 vaccine or a placebo. The study drug or placebo will be administered intramuscularly in the thigh muscle using the TriGrid™ Delivery System version 2.0 (TDS-IM v2.0), a specialized device that applies short, mild electrical pulses (electroporation) to help cells take up the vaccine and stimulate a stronger immune response.

The primary goal of the study is to compare the rate of HPV16 viral clearance between the vaccine and placebo groups at Month 6. The study also features an adaptive design: an interim analysis will be conducted after approximately 50% of participants complete their 6-month assessment. If the initial single-dose regimen shows suboptimal efficacy at the interim stage, the trial may adaptively switch to a two-dose (prime-boost) regimen administered one month apart for the remaining participants. All participants will be closely monitored for safety, side effects, and immune responses for a total duration of 12 months.

Visão geral do estudo

Status

Ainda não está recrutando

Intervenção / Tratamento

Descrição detalhada

STUDY OVERVIEW AND TRIAL DESIGN This study is a randomized, double-blind, placebo-controlled, multicenter Phase II clinical trial in Taiwan to evaluate the safety, efficacy, tolerability, and immunogenicity of the pBI-4 therapeutic DNA vaccine administered via the clinical-stage Intramuscular TriGrid™ Delivery System version 2.0 (TDS-IM v2.0) [1-4]. The target study population consists of adult female subjects aged 19 years and older who have biopsy-confirmed Grade 1 cervical intraepithelial neoplasia (CIN1) with concurrent Human Papillomavirus type 16 (HPV16) infection, or who exhibit persistent (defined as 6 months or longer) HPV16 infection with normal cytology (CIN<1) [5-8].

A maximum target of 94 eligible subjects will be enrolled and randomized in a 1:1 ratio into two parallel groups: 47 subjects in the active pBI-4 vaccine group and 47 subjects in the placebo group [1, 4, 9].

THERAPEUTIC VACCINE AND ELECTROPORATION DELIVERY MECHANISM The investigational drug, pBI-4, is a clinical-grade, 6,999 base-pair circular plasmid DNA vaccine [10-12]. It is engineered to express human calreticulin (CRT) linked to codon-optimized HPV16 E6, E7, and L2 residues (amino acids 11-200) [11]. To ensure clinical safety, the gene sequences encoding the HPV16 E6 and E7 proteins incorporate specific mutations that disable their native oncogenic functions [10, 11, 13].

The vaccine (at a dose of 1.0 mg in 1.0 mL volume) or placebo (1.0 mL of phosphate-buffered saline) is administered intramuscularly into the vastus lateralis (thigh) muscle [1, 14, 15]. To overcome the historical limitation of low cellular DNA uptake in humans, the trial utilizes the automated TDS-IM v2.0 delivery system [14, 16-18]. During the automated administration sequence (which takes approximately 10 seconds), the device deploys an injection needle and four surrounding electrodes into the muscle [19]. Following fluid delivery, short, mild electrical pulses are applied to the local tissue [19]. This electroporation process transiently opens pores in cell membranes, enhancing intracellular plasmid DNA uptake and antigen expression by 2 to 3 orders of magnitude compared to standard needle injections [16, 19, 20].

TWO-STAGE ADAPTIVE REGIMEN MODIFICATION The trial employs a two-stage group-sequential design featuring a pre-specified, non-binding adaptive regimen modification [3, 21]. A single interim analysis will be conducted by an independent Data Safety Monitoring Board (DSMB) once approximately 50% of the randomized participants (approximately 42 patients) complete their Month 6 primary assessment [9, 22].

At the interim analysis, the DSMB will calculate the conditional power (CP) based on the primary efficacy endpoint (HPV16 clearance rate) under the design alternative (assuming a 60% clearance rate in the vaccine group versus a 30% clearance rate in the placebo group) [9, 21, 23].

  • If the conditional power is calculated to be less than 20% (indicating suboptimal efficacy of the single-dose regimen), the trial will trigger a non-binding futility rule and adaptively switch to a two-dose (prime-boost) regimen for all remaining participants enrolled in Stage 2 [21]. Under this adapted schedule, Stage 2 participants will receive their first dose at Month 0 and a booster dose at Month 2, while maintaining double-blind placebo control and 1:1 randomization [21, 24].
  • If the conditional power is 20% or higher, the trial will continue with the original single-dose regimen for the rest of the study [21].

CLINICAL EVALUATIONS AND FOLLOW-UP TIMELINE

All participating subjects will undergo structured clinical assessments across multiple visits:

  1. Baseline/Screening (Month -1 to 0): Obtaining written informed consent, checking full eligibility, medical and gynecological history, physical examination with ECOG performance status, vital signs, clinical laboratory tests (including complete blood count with differential, serum chemistry, HIV, Hepatitis B and C screenings), urine pregnancy test, Pap smear, Roche Cobas HPV genotyping, and colposcopy with endocervical curettage (ECC) and mandatory tissue biopsy [6, 25-27].
  2. Vaccination Visit (Month 0 Day 1): Pre-dose physical exam, vital signs, urine pregnancy test, and a research blood draw (serum and peripheral blood mononuclear cells) for baseline HPV16-specific humoral and cell-mediated immune assessments [14, 28-30]. Following the pBI-4 or placebo injection via TDS-IM v2.0, subjects are observed on-site for up to 60 minutes, with vital signs recorded at 30 and 60 minutes post-dose to monitor for potential immediate hypersensitivity or vasovagal reactions [14, 30-32].
  3. Post-Vaccination Phone Call (Week 1 / Day 8): A telephone interview to record any local reactogenicity, systemic adverse events, and concomitant medications, alongside the administration of the Procedure Tolerability Questionnaire to measure pain (using a 10-point Visual Analog Scale) and device acceptability [29, 31-33].
  4. Month 6 Follow-Up Visit: Physical exam, vital signs, safety laboratory tests, research blood draw for immunologic response, Pap smear, Roche Cobas HPV genotyping, and colposcopy with ECC (with biopsy performed only if clinically indicated) [29, 34-36].
  5. Month 12 Follow-Up Visit (Final Evaluation): A replication of the Month 6 visit assessments, representing the completion of the 12-month post-vaccination follow-up period.

If the adaptive two-dose regimen is triggered, Stage 2 participants will undergo an additional vaccination visit at Month 2 Day 1 (with pre-dose safety labs and a pregnancy test) and a subsequent post-vaccination telephone call at Week 9 to document tolerability and safety parameters [24, 40].

Tipo de estudo

Intervencional

Inscrição (Estimado)

94

Estágio

  • Fase 2
  • 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

Locais de estudo

    • Kaohsiung
      • Kaohsiung City, Kaohsiung, Taiwan, 833
        • Kaohsiung Chang Gung Memorial Hospital
        • Contato:
    • Taoyuan
      • Taoyuan, Taoyuan, Taiwan, 333
        • Linkou Chang Gung Memorial Hospital
        • 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:

  • Patients with CIN1 on biopsy and whose cytologic sample is HPV16+ by Roche Cobas test in the past 30 days, OR patients with CIN<1 on biopsy whose cytologic sample is HPV16+ by Roche Cobas test in the past 30 days and a history of a second HPV16+ test at least 6 months prior

    • (Co-infections with HPV types other than HPV16 are permissible for study entry)
    • Age ≥ 19 years
    • Baseline Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 at the time of study treatment administration
    • Adequate organ function at the time of enrollment as defined by:

White blood cell count > 3,000/mcL Absolute lymphocyte number > 500/mcL Absolute neutrophil count > 1,000/mcL Platelets > 90,000/mcL Hemoglobin > 9 g/dL Total bilirubin < 3 x institutional limit of normal AST(SGOT)/ALT(SGPT) < 3 x institutional limit of normal Creatinine < 2.5 x institutional limit of normal Women of child-bearing potential must agree to use effective contraception (hormonal and/or barrier) prior to study entry and for the duration of the study

  • Ability to understand and willingness to sign a written informed consent document
  • Subject is able to adhere to the study visit schedule and other protocol requirements

Exclusion Criteria:

  • Patients with AIS (adenocarcinoma in situ) or cancer determined by cervical cytology at study entry

    • Histologic evidence of CIN2 or above
    • Patients with a diagnosis of immunosuppression or prolonged, active use of immunosuppressive medications such as steroids
    • Prior treatment with any HPV therapeutic agent (e.g., Imiquimod, Veregen, Podophylotoxin)
    • Patients who are receiving any other investigational agents or blood products within 30 days prior to the first dose
    • Patients with an uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance
    • Patients with a history of autoimmune disease such as multiple sclerosis (exclusive of a history of thyroiditis, psoriasis, Sjogren's, or inflammatory bowel disease)
    • Patients with a history of allergic reactions attributed to compounds used in agent preparation
    • Patients who are pregnant or breast feeding
    • Patients with active or chronic infection of HIV, HCV, or HBV
    • Patients who have had a prior LEEP or cervical conization procedure
    • History of prior malignancy (permitted only if the patient has been disease-free for ≥ 5 years, or has completely resected basal cell or squamous cell carcinoma of the skin)
    • Less than 1 acceptable potential injection site for intramuscular injection and electroporation (considering the left/right medial deltoid, and anterolateral quadriceps muscles)
    • A site is unacceptable if there is inadequate muscle mass to support at least a 19 mm (0.75 inch) injection depth or a skinfold thickness of ≥ 50 mm
    • (Note: For participants weighing ≤ 65 kg, acceptable sites are confined to the outer aspect of the upper thigh, and the deltoids are not eligible)
    • Contraindication to intramuscular injections and blood draws
    • A metal implant or implantable device within the area of the electroporation injection site at > 2 of the eligible injection sites .A nonremovable electronic stimulation device (such as cardiac demand pacemakers, automatic implantable cardiac defibrillators, nerve stimulators, or deep brain stimulators).

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: Quadruplicar

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador de Placebo: Placebo
A clinical-grade, 6,999 base-pair circular recombinant plasmid DNA vaccine (pBI-4) engineered to express human calreticulin (CRT) linked to codon-optimized HPV16 E6, E7, and L2 residues (amino acids 11-200). To ensure clinical safety, E6 and E7 incorporate inactivating mutations to disable their native oncogenic transforming activities. Administered at a dose of 1.0 mg (1.0 mL) intramuscularly into the thigh muscle using the TDS-IM v2.0 electroporation device.
Experimental: pBI-4 Vaccine
A clinical-grade, 6,999 base-pair circular recombinant plasmid DNA vaccine (pBI-4) engineered to express human calreticulin (CRT) linked to codon-optimized HPV16 E6, E7, and L2 residues (amino acids 11-200). To ensure clinical safety, E6 and E7 incorporate inactivating mutations to disable their native oncogenic transforming activities. Administered at a dose of 1.0 mg (1.0 mL) intramuscularly into the thigh muscle using the TDS-IM v2.0 electroporation device.
A clinical-grade, 6,999 base-pair circular recombinant plasmid DNA vaccine (pBI-4) engineered to express human calreticulin (CRT) linked to codon-optimized HPV16 E6, E7, and L2 residues (amino acids 11-200). To ensure clinical safety, E6 and E7 incorporate inactivating mutations to disable their native oncogenic transforming activities. Administered at a dose of 1.0 mg (1.0 mL) intramuscularly into the thigh muscle using the TDS-IM v2.0 electroporation device.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Proportion of subjects exhibiting virological clearance of HPV16 and histopathological regression of cervical lesions to < CIN2 at Month 6
Prazo: Month 6 (or 6 months post-vaccination)
The proportion of subjects with histopathologically confirmed HPV16-associated CIN2 or CIN3 who exhibit virological clearance of HPV16 and regression of cervical lesions to < CIN2 at Month 6.
Month 6 (or 6 months post-vaccination)

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 (Estimado)

1 de setembro de 2026

Conclusão Primária (Estimado)

1 de março de 2030

Conclusão do estudo (Estimado)

1 de março de 2030

Datas de inscrição no estudo

Enviado pela primeira vez

11 de agosto de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

8 de setembro de 2026

Primeira postagem (Real)

9 de setembro de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

14 de setembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

10 de setembro de 2026

Última verificação

1 de setembro de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • TGOG1018

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Descrição do plano IPD

No individual participant data will be shared with persons other than the investigators of this study to protect participant confidentiality.

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

produto fabricado e exportado 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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