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Study of the TheraBionic P1 Device in Patients With Metastatic Triple Negative Breast Cancer After Progression

19 de junho de 2026 atualizado por: Jailan Elayoubi, Barbara Ann Karmanos Cancer Institute

A Pilot Study of the Efficacy of the TheraBionic P1 Device in Patients With Metastatic Triple Negative Breast Cancer in the Third-line Setting

The goal of this clinical trial is to learn if adding the TheraBionic P1 device to standard of care third line treatment for adult women with metastatic triple negative breast cancer (mTNBC) who have failed, not tolerated, or progressed on standard first- and second-line treatment options can work better than the standard of care alone. The main questions it aims to answer is:

  • will the addition of the TheraBionic P1 device to standard of care third line treatment affect progression free and overall survival in these participants

Visão geral do estudo

Status

Ainda não está recrutando

Intervenção / Tratamento

Tipo de estudo

Intervencional

Inscrição (Estimado)

24

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.

Contato de estudo

Locais de estudo

    • Michigan
      • Detroit, Michigan, Estados Unidos, 48201
        • Karmanos Cancer Institute
        • Contato:
          • Jailan Elayoubi, M.D.
          • Número de telefone: 1-800-527-6266

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:

  • Participant must have histologically confirmed invasive breast cancer that is hormone receptor (HR) negative and Human Epidermal Growth Factor Receptor 2 (HER2) negative according to the American Society of Clinical Oncology (ASCO) College of American Pathologists (CAP) guidelines (Estrogen Receptor (ER) and progesterone receptor (PR) < 1% and HER2 negative by immuno-histochemistry (IHC) and/or fluorescent in situ hybridization [FISH]
  • Participant must have evaluable disease as defined by the investigator using CT, MRI, or positron emission tomography (PET) scan
  • Participant must have refractory disease and failed, not tolerated, or progressed on at least two lines of prior standard therapeutic regimens for mTNBC.

    • Participant must have a washout period of at least 14 days between the last line of treatment and the start of study treatment.

  • Participant must be a woman of 22 years of age or older.
  • Participant must have a life expectancy of at least three months
  • Participant must have an Eastern Cooperative Oncology Group (ECOG) performance score of 0-2
  • It is unknown what effects this treatment has on human pregnancy or development of the embryo or fetus. Therefore, women of child-bearing potential must agree to avoid becoming pregnant and male participants should avoid impregnating a female partner and donating sperm starting at initiation of treatment up until at least 12 weeks after treatment discontinuation

    • Surgically sterile (hysterectomy, bilateral oophorectomy, or bilateral salpingectomy)
    • Post-menopausal, defined as no menses for at least 12 months prior to the screening visit without alternative medical causation.
    • Agree to practice true abstinence from sexual intercourse when this is in line with the preferred and usual lifestyle of the participant. Periodic abstinence methods such as calendar, ovulation, symptothermal, or post ovulation tracking are not acceptable.
    • Not in a sexual relationship in which they may become pregnant (i.e. same-sex relationship)
    • If they are of child-bearing potential, agree to use at least one highly effective AND at least one additional method of contraception. Withdrawal is not an acceptable contraceptive method.

Exclusion Criteria:

  • Participants with known active secondary malignancy, unless, in the opinion of the investigator, it is unlikely to interfere with the safety and efficacy of the endpoints.
  • Participants with known untreated brain metastases will be excluded from this clinical trial. Stable brain metastases will be allowed, and it will be confirmed by stable brain magnetic resonance imaging (MRI) with and without contrast within 8 weeks of signing consent.
  • Participants who are taking any other investigational drugs
  • Participants who are pregnant or breastfeeding. If a breastfeeding participant would like to be part of this study, breastfeeding must be discontinued
  • Participants with active oral mucosal inflammation, ulceration, or other pathology that could interfere with the use of TheraBionic P1 device (for example: mucositis, thrush, bleeding mucosal lesions, oral herpes, aphthous stomatitis, mouth ulcers, chancre sores, gingivostomatitis, herpangina, aphthae).
  • Participants who plan to receive calcium channel blockers and any agent blocking L-type of T-type voltage gated calcium channels (for example: amlodipine, nifedipine, ethosuximide, supplemental vitamin C/ascorbic acid, etc.) unless their medical treatment is discontinued prior to treatment. Participant must agree to abstain from using calcium channel blockers for the duration of treatment on study
  • Participants who plan to receive anticancer therapy that blocks L-type or T-type voltage gated calcium channels (i.e., eribulin, rucaparib, or niraparib) as part of their third line treatment. Participants who have received eribulin, rucaparib, or niraparib as part of a previous line of therapy are eligible, provided there has been at least 14 days between the last date of treatment and the start of study treatment.
  • Participants that do not agree to be followed according to the study protocol or have cognitive or physical inability to follow the treatment plan
  • Participants with a known severe (e.g., anaphylactic) allergy to nickel

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: N / D
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Amplitude-modulated radiofrequency electromagnetic fields device plus third line treatment
TheraBionic P1 amplitude-modulated radiofrequency electromagnetic fields device 3 times daily (continuous) plus standard of care third line treatment
TheraBionic P1 is amplitude-modulated radiofrequency electromagnetic fields (AM RF EMF) device added to any third line treatment for triple negative breast cancer

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
6 month Progression Free Survival (PFS6)
Prazo: 6 months after start of treatment
PFS is defined as the interval from treatment initiation to the date of disease progression of death from any cause, whichever occurs first. The treating investigator will determine disease progression. PFS6 will be calculated as the proportion of participants who are alive without progression at six months post-treatment initiation.
6 months after start of treatment

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Changes in Quality of Life Scores (QOL)
Prazo: From baseline to up to 1 year after treatment initiation
QOL scores are evaluated using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (EORTC QLQ - C30). It is 30-item questionnaire assessing cancer patients' health-related quality of life, covering functional scales (physical, role, emotional, cognitive, social), symptom scales (fatigue, pain, nausea, dyspnoea, etc.), and a global health/QoL scale. We will record the time to deterioration of QOL, physical functioning, and role functioning, as reported by the participant, with deterioration defined as a decrease from baseline of 10 points or more on the EORTC QLQ - C30 maintained for two consecutive assessments or a decrease of 10 points or more in one assessment followed by death from any cause within three weeks.
From baseline to up to 1 year after treatment initiation
Overall Survival (OS)
Prazo: From baseline to up to 5 years after treatment initiation
Participants will be followed for survival status every six months for five years after treatment is initiated. OS is defined as the interval from treatment initiation to the date of death from any cause. The distribution of time-to-event data (OS) will be graphically summarized using a Kaplan-Meier (KM) curve, with corresponding median and two-sided 95% Confidence Level (CI) computed using KM estimates. OS rates every six months post-treatment will be estimated using KM estimates with two-sided 95% CIs provided for each time point.
From baseline to up to 5 years after treatment initiation
Progression Free Survival
Prazo: From baseline to up to 5 years after treatment initiation
Participants will be followed for progression status every six months for five years after treatment is initiated. Participants will not be followed for progression if they start another anti-cancer therapy during this time. PFS is defined as the interval from treatment initiation to the date of disease progression of death from any cause, whichever occurs first. The treating investigator will determine disease progression. The distribution of time-to-event data (PFS) will be graphically summarized using a Kaplan-Meier (KM) curve, with corresponding median and two-sided 95% CI computed using KM estimates. PFS rates every six months post-treatment will be estimated using KM estimates with two-sided 95% CIs provided for each time point.
From baseline to up to 5 years after treatment initiation

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Jailan Elayoubi, M.D., Barbara Ann Karmanos Cancer Institute

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)

31 de dezembro de 2028

Conclusão do estudo (Estimado)

31 de dezembro de 2028

Datas de inscrição no estudo

Enviado pela primeira vez

19 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

19 de junho de 2026

Primeira postagem (Real)

29 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

29 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

19 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Palavras-chave

Outros números de identificação do estudo

  • 2025-103

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

Sim

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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