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Efficacy and Safety of MitoQ in Improving Cancer Cachexia

17 de setembro de 2026 atualizado por: Yinghua Ji, The First Affiliated Hospital of Xinxiang Medical College

Efficacy and Safety of MitoQ in Improving Cancer Cachexia: A Clinical Study

Muscle strength was evaluated in subjects with malignant solid tumors and cachexia after 12 weeks of oral MitoQ treatment.

Visão geral do estudo

Descrição detalhada

Primary Efficacy Endpoint:

To evaluate the preliminary efficacy of MitoQ in patients with cancer cachexia by comparing muscle function before and after MitoQ administration at Weeks 7 and 13, as assessed by handgrip strength and the 6-minute walk test (6MWT).

Key Secondary Efficacy Endpoints:

Inflammatory and Metabolic Markers: Changes in the levels of C-reactive protein (CRP), interleukin-6 (IL-6), and tumor necrosis factor-alpha (TNF-α); effects on oxidative stress markers (MDA, SOD, GPx); and levels of prealbumin and serum albumin.

Clinical Benefit Endpoints:

Changes in skeletal muscle mass at Weeks 7 and 13, as measured by the skeletal muscle index (SMI) at the third lumbar vertebra (L3) level using computed tomography (CT), as well as changes in body weight, including total body weight, fat mass, and lean body mass.

Quality of life and symptom assessment using validated instruments: the EORTC QLQ-C30 (quality of life), the Functional Assessment of Anorexia/Cachexia Therapy (FAACT), the Hospital Anxiety and Depression Scale (HADS), and the Cancer Fatigue Scale (CFS).

Other Secondary Efficacy Endpoints:

Tumor Response and Survival Endpoints: Objective response rate (ORR) based on RECIST version 1.1 criteria and progression-free survival (PFS).

Safety Assessment: Hepatic function tests and lipid profile. Exploratory Endpoints: Exploratory biomarkers including metabolic and inflammatory factors.

Safety Endpoints:

Vital signs, physical examination, laboratory parameters, electrocardiogram (ECG), echocardiography, and adverse events (AEs), with AEs graded according to the NCI Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.

Tipo de estudo

Intervencional

Inscrição (Estimado)

20

Estágio

  • Fase 2

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: Yinghua Ji
  • Número de telefone: +8613663030446
  • E-mail: 54234317@qq.com

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

18 anos e mais velhos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  • Subjects must meet all of the following inclusion criteria at screening to be eligible for enrollment in this study:

Subjects aged ≥ 18 years at the time of screening. Subjects who are willing and able to comply with all scheduled visits, treatment plans, laboratory tests, and other study procedures.

Ability to sign the informed consent form. Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2. Life expectancy of more than 3 months. Patients with histologically or cytologically confirmed malignant solid tumors (patients with hepatocellular carcinoma may be enrolled based on clinical diagnosis).

Medically documented cachexia or pre-cachexia (patient-reported weight loss data are acceptable for patients receiving first-line treatment):

Cachexia: Involuntary weight loss of >5% within 6 months prior to screening. Pre-cachexia: Involuntary weight loss of ≤5% within 6 months prior to screening, accompanied by anorexia or metabolic alterations.

Adequate organ function, as defined by the following:

Serum total bilirubin ≤ 1.5 × upper limit of normal (ULN), unless the subject has a confirmed diagnosis of Gilbert's syndrome.

Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 × ULN; if tumor involves the liver, ≤ 5.0 × ULN.

Creatinine ≤ 2 mg/dL, or glomerular filtration rate (GFR) ≥ 30 mL/min/1.73 m², calculated according to the Modification of Diet in Renal Disease (MDRD) formula.

Subjects of childbearing potential must agree to use at least one medically acceptable and effective method of contraception during sexual intercourse throughout the study period and for 6 months after the last dose of study drug, and must have no plans for pregnancy or sperm/egg donation.

Subjects who clearly understand the study, voluntarily agree to participate, and sign the informed consent form personally.

Exclusion Criteria:

  • Subjects presenting with any of the following at screening will not be eligible for enrollment in this study:

Known hypersensitivity to MitoQ capsules or any of the excipients. Subjects with known symptomatic brain metastases requiring regular use of corticosteroids. Asymptomatic or previously diagnosed brain metastases may be included if the following conditions are met: treatment has been completed, and the subject has recovered from acute effects of radiation therapy or surgery prior to screening; corticosteroid therapy for brain metastases has been discontinued, and the neurological status is stable prior to the first dose of study drug.

Known active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection (subjects with HBV-DNA < 10⁴ IU/mL may be enrolled).

Known positive test for human immunodeficiency virus (HIV) or positive treponemal antibody (TP-Ab) test.

Currently existing reversible reduction in food intake, as determined by the investigator, including but not limited to:

National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) Grade 3 or 4 oral mucositis; NCI CTCAE Grade 3 or 4 gastrointestinal (GI) disorders (e.g., nausea, vomiting, diarrhea, and constipation); Mechanical obstruction preventing oral intake. Receiving tube feeding or parenteral nutrition (whether total or partial parenteral nutrition) at the time of screening.

Major surgery within 4 weeks prior to the first dose of study drug (central venous access device placement and tumor biopsy are not considered major surgery); subjects must have adequately recovered from the acute effects of surgery prior to screening, and no major surgery should be planned during the study period.

Severe gastrointestinal disorders (including esophagitis, gastritis, and malabsorption).

History of subtotal gastrectomy or small bowel resection (more than one-third).

Cachexia caused by other conditions, as determined by the investigator, including but not limited to:

Severe chronic obstructive pulmonary disease (COPD); New York Heart Association (NYHA) Class III or IV heart failure; Acquired immunodeficiency syndrome (AIDS). Any of the following events within the past 3 months: myocardial infarction, congenital long QT syndrome, torsades de pointes, cardiac arrhythmia (including sustained ventricular tachycardia and ventricular fibrillation), unstable angina, coronary artery or peripheral artery bypass graft, symptomatic congestive heart failure (CHF, NYHA Class III or IV), severe cerebrovascular accident, or symptomatic pulmonary embolism or other clinically significant cardiovascular/thromboembolic disease.

Persistent malignant arrhythmia of NCI CTCAE Grade ≥ 2. Initiation of new systemic corticosteroid therapy within 4 weeks prior to the first dose of study drug. Stable corticosteroid therapy (i.e., no significant change in dose or frequency of administration within 4 weeks prior to the first dose) is permitted, such as dexamethasone used as a premedication or daily oral prednisone.

Planned anti-tumor therapy during the study that includes agents known to cause weight gain, such as ALK inhibitors, ROS1 inhibitors, or docetaxel, within 4 weeks or 5 half-lives of the drug (whichever is longer) prior to the first dose of study drug.

Use of any prescription medication that increases appetite or ameliorates weight loss within 4 weeks or 5 half-lives of the drug (whichever is longer) prior to the first dose of study drug, including but not limited to anamorelin, medroxyprogesterone acetate, dronabinol, medical cannabis, etc.

Currently receiving another investigational drug, or use of another investigational drug within 4 weeks prior to the first dose of study drug or within 5 half-lives of the previous investigational drug (whichever is longer).

Female subjects who are pregnant or breastfeeding. Any other acute or chronic medical or psychiatric condition, including recent (within the past year) or active suicidal ideation or behavior, or laboratory abnormalities that may increase the risk associated with study participation or use of the study drug, or that may interfere with the interpretation of study results. The investigator may exclude a subject from participation if, in the investigator's judgment, the subject is unsuitable for enrollment in this study for any of these reasons.

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: MITOQ group

MitoQ 20 mg/day (one 20 mg capsule), administered orally once daily in the morning on an empty stomach.

MitoQ 20 mg/day (one 20 mg capsule), administered orally once daily in the morning on an empty stomach.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
To evaluate the preliminary efficacy of MitoQ in patients with cancer cachexia
Prazo: 0-13 Weeks

To evaluate the preliminary efficacy of MitoQ in patients with cancer cachexia by comparing muscle function before and after MitoQ administration at Weeks 13, as assessed by handgrip strength.

0-13 Weeks

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Inflammatory and Metabolic Markers
Prazo: 0-13 Weeks

Changes in the levels of C-reactive protein (CRP).

0-13 Weeks
Clinical Benefit Endpoints
Prazo: 0-13 Weeks

Changes in skeletal muscle mass at Weeks 13, as measured by the skeletal muscle index (SMI) at the third lumbar vertebra (L3) level using computed tomography (CT).

0-13 Weeks
Clinical Benefit Endpoints
Prazo: 0-13 weeks

Quality of life and symptom assessment using validated instruments: the EORTC QLQ-C30 (quality of life).

0-13 weeks

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)

10 de outubro de 2026

Conclusão Primária (Estimado)

10 de outubro de 2026

Conclusão do estudo (Estimado)

1 de junho de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

14 de agosto de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

17 de setembro de 2026

Primeira postagem (Real)

23 de setembro de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

23 de setembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

17 de setembro de 2026

Última verificação

1 de agosto de 2026

Mais Informações

Termos relacionados a este estudo

Termos MeSH relevantes adicionais

Outros números de identificação do estudo

  • CHASE 019

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

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

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