- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07612007
HRX215, A First Generation MKK4 Inhibitor Drug, for the Treatment of Patients With Colorectal Liver Metastasis After Undergoing a Portal Vein Embolization
Phase 2B Study to Determine Efficacy of HRX215, a First Generation MKK4 Inhibitor Drug, in Improving Regeneration of the Remnant Liver After Portal Vein Embolization (PVE) of Colorectal Liver Metastasis (CRLM)
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
- Procedimento: Imagem de ressonância magnética
- Procedimento: Coleta de bioespécimes
- Medicamento: Administração de Placebo
- Procedimento: Procedimento de biópsia
- Procedimento: Computed Tomography
- Medicamento: Darizmetinib
- Medicamento: Embolization Therapy
- Procedimento: Hepatectomy
- Procedimento: Positron Emission Tomography
Tipo de estudo
Inscrição (Estimado)
Estágio
- Fase 2
Contactos e Locais
Contato de estudo
- Nome: Clinical Trials Referral Office
- Número de telefone: 855-776-0015
- E-mail: mayocliniccancerstudies@mayo.edu
Estude backup de contato
- Nome: Cancer Center Clinical Trials Referral Office
- Número de telefone: 507-293-6386
Locais de estudo
-
-
Minnesota
-
Rochester, Minnesota, Estados Unidos, 55905
- Mayo Clinic in Rochester
-
Contato:
- Clinical Trials Referral Office
- Número de telefone: 855-776-0015
- E-mail: mayocliniccancerstudies@mayo.edu
-
Contato:
- Cancer Center Clinical Trials Referral Office
- Número de telefone: 507-293-6386
-
Investigador principal:
- Scott L. Nyberg, MD, PhD
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria:
- REGISTRATION: Adults 18-90 years
- REGISTRATION: Individuals with metachronous colorectal carcinoma liver metastases (CRCLM) after resection of the primary OR synchronous CRCLM with planned simultaneous resection of primary and metastatic disease
- REGISTRATION: Measurable intrahepatic disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST) and considered resectable by multidisciplinary tumor board with at least one senior hepatic surgeon
- REGISTRATION: Available CT suitable for volumetric studies on FLR ≤ 21 days
- REGISTRATION: Clinical indication for PVE prior to major hepatectomy as evaluated by at least one senior hepatic surgeon
- REGISTRATION: Estimated life expectancy ≥ 3 months as evaluated and approximated by a senior hepatic surgeon
- REGISTRATION: Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0-1
- REGISTRATION: Platelets ≥ 100,000/mm^3 (≤ 15 days prior to registration)
- REGISTRATION: Polynuclear neutrophils ≥ 1000/mm^3 (≤ 15 days prior to registration)
- REGISTRATION: Hemoglobin ≥ 9 g/dL (≤ 15 days prior to registration) (post-transfusion participants can be included)
- REGISTRATION: Creatinine ≤ 1.5 x upper limit of normal (ULN) (≤ 15 days prior to registration)
- REGISTRATION: Bilirubin ≤ ULN (≤ 15 days prior to registration)
- REGISTRATION: Albumin ≥ 3 g/dL (≤ 15 days prior to registration)
- REGISTRATION: Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 3 x ULN (≤ 15 days prior to registration)
- REGISTRATION: International normalized ratio ≤ 1.5 (≤ 15 days prior to registration)
- REGISTRATION: Of note, a slight deviation from normal ranges of liver function tests, circulating cell counts, and kidney function can be assumed after systemic neoadjuvant chemotherapy prior to PVE (Field et al., 2008; Takamoto et al., 2010; Lock et al., 2017), which is accounted for in the above list. These parameters at inclusion will then serve as patient baseline
- REGISTRATION: Negative pregnancy test done ≤ 7 days prior to registration, for persons of childbearing potential only. Serum or urine human chorionic gonadotropin test is suitable. Can be done with a home test and results reported by participant to the site
- REGISTRATION: Provide written informed consent
- REGISTRATION: Willing to return to enrolling institution for follow-up (during the active monitoring phase of the study)
- RANDOMIZATION: Adults 18-90 years
- RANDOMIZATION: Individuals with metachronous CRCLM after resection of the primary OR synchronous CRCLM with planned simultaneous resection of primary and metastatic disease
- RANDOMIZATION: Estimated life expectancy ≥ 3 months as evaluated and approximated by a senior hepatic surgeon
- RANDOMIZATION: Measurable intrahepatic disease as defined by RECIST and considered resectable by multidisciplinary tumor board with at least one senior hepatic surgeon
- RANDOMIZATION: Available CT suitable for volumetric studies on FLR ≤ 21 days
- RANDOMIZATION: Scheduled for PVE prior to major hepatectomy
Exclusion Criteria:
- REGISTRATION: Cirrhosis or clinical ascites
- REGISTRATION: Patients with synchronous CRCLM and scheduled staged approach (i.e., resection of metastatic hepatic disease after PVE followed by resection of the colorectal primary in a second operation)
- REGISTRATION: Any liver cancer other than CRLM
REGISTRATION: Contraindications to imaging or perioperative management:
- Allergy/contraindication to iodine contrast
- Anticoagulation with heparin/antivitamin K (AVK) that cannot be interrupted for 48 hours
- Antiplatelet therapy (e.g., clopidogrel) that cannot be interrupted for 5 days
- REGISTRATION: Inability to discontinue cytochrome P450 (CYP)2D6 inhibitor concomitant medication from start of trial treatment to day 28
- REGISTRATION: Inoperability due to underlying chronic diseases and co-morbidities as assessed by the hepatobiliary surgeon during screening visit
- REGISTRATION: Anticipated need to start adjuvant chemotherapy prior to completion of 28 day treatment period
- REGISTRATION: Positive test at screening for active hepatitis B virus (HBV)/hepatitis C virus (HCV), defined as history of seropositivity for hepatitis B virus (unless immune due to vaccination or resolved natural infection or unless passive immunization due to immunoglobulin therapy), i.e., positive test for anti-hepatitis B core antigen and negative test for anti-hepatitis B surface antibody. Ongoing, non-cured hepatitis C virus (HCV) infection. Likewise, autoimmune hepatitis will be excluded based on serological [antinuclear antibodies (ANA), smooth muscle antibodies (SMA), and biochemical parameters AST and ALT], patients with serological and/or biochemical findings suggestive of probable autoimmune hepatitis will be excluded
- REGISTRATION: Legal incapacity (persons in custody or under guardianship)
- REGISTRATION: Deprived of liberty subject (by judicial or administrative decision)
- REGISTRATION: Impossibility to sign the informed consent document or to adhere to the medical follow-up of the trial for geographical, social, or psychological reasons
REGISTRATION: Any of the following because this study involves an investigational agent, the genotoxic, mutagenic and teratogenic effects of which on the developing fetus and newborn are unknown
- Pregnant persons
- Nursing persons
- Persons of childbearing potential who are unwilling to employ adequate contraception. Participants of childbearing potential must use highly effective contraception (hormonal methods, intrauterine device (IUD)/intrauterine system (IUS), bilateral tubal occlusion, or vasectomized partner) during treatment and for a defined post-treatment period of 30 days. True abstinence is acceptable if consistent with lifestyle. Barrier methods alone are insufficient unless combined. Male participants with partners of childbearing potential must use condoms and avoid sperm donation during and after treatment
REGISTRATION: Any of the following prior therapies:
- Major surgical procedures ≤ 3 weeks prior to registration
- Bevacizumab as part of systemic cancer treatment ≤ 2 weeks prior to registration
REGISTRATION: Failure to recover from any adverse events related to any of the following therapies received prior to registration:
- Chemotherapy
- Immunotherapy
- Targeted therapies
- Other investigational agents
- Radiation therapy
- Major surgical procedures
- REGISTRATION: Co-morbid systemic illnesses or other severe concurrent disease which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens
REGISTRATION: Uncontrolled intercurrent illness including, but not limited to:
- Ongoing or active infection
- Symptomatic congestive heart failure
- Unstable angina pectoris
- Cardiac arrhythmia
- Dyspnea at rest due to complications of advanced malignancy or other disease that requires continuous oxygen therapy
- Psychiatric illness/social situations that would limit compliance with study requirements
REGISTRATION: Immunocompromised patients and patients known to be HIV positive and currently receiving antiretroviral therapy
- NOTE: Patients known to be HIV positive, but without clinical evidence of an immunocompromised state, are eligible for this trial
- REGISTRATION: Receiving any other investigational agent which would be considered as a treatment for the primary neoplasm in the neoadjuvant setting or during active treatment phase of this study (adjuvant treatment after active treatment phase is completed does not apply)
- REGISTRATION: Another active malignancy requiring therapy such as radiation, chemotherapy, or immunotherapy at time of study inclusion or within the past five years with the exception of basal cell carcinoma or carcinoma in situ of the cervix. Patients on hormonal therapy for treated breast or prostate cancer are permitted if they meet other eligibility criteria
- REGISTRATION: History of myocardial infarction ≤ 6 months, or congestive heart failure requiring use of ongoing maintenance therapy for life-threatening ventricular arrhythmias
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: Randomizado
- Modelo Intervencional: Atribuição Paralela
- Mascaramento: Triplo
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: Arm I (HRX215, PVE, hepatectomy)
Patients undergo scheduled PVE on day 0. Starting 2 hours before undergoing PVE, patients receive HRX215 PO BID (orally twice daily) on days 0-27 in the absence of disease progression or unacceptable toxicity.
Starting on or after day 32, patients may undergo scheduled hepatectomy.
Patients also undergo blood sample collection, CT, MRI, and CT-PET throughout the study.
Additionally, patients may undergo tissue biopsy during scheduled hepatectomy on study.
|
Submeter-se a ressonância magnética
Outros nomes:
Realizar coleta de sangue
Outros nomes:
Sofre biópsia tecidual
Outros nomes:
Undergo CT and CT-PET
Outros nomes:
Given PO
Outros nomes:
Undergo PVE
Outros nomes:
Undergo hepatectomy
Outros nomes:
Undergo CT-PET
Outros nomes:
|
|
Comparador de Placebo: Arm II (placebo, PVE, hepatectomy)
Patients undergo scheduled PVE on day 0. Starting 2 hours before undergoing PVE, patients receive placebo PO BID (orally twice daily) on days 0-27 in the absence of disease progression or unacceptable toxicity.
Starting on or after day 32, patients may undergo scheduled hepatectomy.
Patients also undergo blood sample collection, CT, MRI, and CT-PET throughout the study.
Additionally, patients may undergo tissue biopsy during scheduled hepatectomy on study.
|
Submeter-se a ressonância magnética
Outros nomes:
Realizar coleta de sangue
Outros nomes:
Dado PO
Sofre biópsia tecidual
Outros nomes:
Undergo CT and CT-PET
Outros nomes:
Undergo PVE
Outros nomes:
Undergo hepatectomy
Outros nomes:
Undergo CT-PET
Outros nomes:
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Future liver remnant size (FLR)
Prazo: At day 28 post-baseline
|
Will be defined as the percentage of the liver expected to remain after a planned hepatectomy.
Will be compared between the two treatment groups [HRX215 versus (vs) placebo] utilizing an analysis of covariance (ANCOVA) F-test controlling for age, gender, and FLR at baseline.
|
At day 28 post-baseline
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
FLR size
Prazo: At day 7 post-baseline
|
Will be defined as the percentage of the liver expected to remain after a planned hepatectomy.
Will be compared between the two treatment groups (HRX215 vs placebo) utilizing an ANCOVA F-Test controlling for age, gender, and FLR at baseline.
|
At day 7 post-baseline
|
|
Incidence of adverse events (AEs)
Prazo: Up to 28 days after last dose of study treatment
|
AEs will be graded using Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0.
Each type of AE and grade will be recorded for each patient.
The distribution of serious AEs as well as AEs of special interest will be compared between treatment arms descriptively to look for trends.
|
Up to 28 days after last dose of study treatment
|
|
Resectability after PVE
Prazo: At or after 28 days post-baseline
|
The proportion of patients will be compared between treatment arms utilizing a Chi-Square test.
|
At or after 28 days post-baseline
|
|
Post-hepatectomy liver failure (PHLF)
Prazo: Between postoperative days 5 and 7
|
Will be defined according to the criteria issued by the International Study Group for Liver Surgery (ISGLS).
Grading of PHLF into grades A to C will be performed, and grades B-C will be defined as severe PHLF.
The proportion of patients will be compared between treatment arms utilizing a Chi-Square test.
|
Between postoperative days 5 and 7
|
|
Post-operative mortality
Prazo: Up to the first 90 days after liver resection
|
Defined as patient death within the first 90 days after liver resection.
The proportion of patients will be compared between treatment arms utilizing a Chi-Square test.
|
Up to the first 90 days after liver resection
|
|
Recurrence-free survival (RFS)
Prazo: From major liver resection to disease recurrence, assessed up to 360 days
|
Defined as the time from major liver resection to disease recurrence.
Will be analyzed using the Kaplan-Meier Method.
The distribution of RFS will be compared between treatment arms utilizing a two-sided log-rank test.
|
From major liver resection to disease recurrence, assessed up to 360 days
|
|
Overall survival (OS)
Prazo: From randomization to death from any cause, assessed up to 360 days
|
Defined as the time from randomization to death from any cause.
Will be analyzed using the Kaplan-Meier Method.
The distribution of OS will be compared between treatment arms utilizing a two-sided log-rank test.
|
From randomization to death from any cause, assessed up to 360 days
|
|
Post-operative morbidity
Prazo: Up to 360 days post-PVE
|
Will be defined according to the system issued in "Classification of surgical complications: a new proposal with evaluation in a cohort of 6336 patients and results of a survey," a standardized, therapy-oriented system for grading postoperative surgical complications according to the treatment required to manage them rather than subjective severity.
Complications range from Grade I, defined as any deviation from the normal postoperative course not requiring specific therapy, to Grade V, defined as death.
Intermediate grades reflect increasing therapeutic intensity, from pharmacological treatment (Grade II), to interventions with or without general anesthesia (Grade III), and life-threatening complications requiring intensive care (Grade IV)..
The proportion of patients will be compared between treatment arms utilizing a Chi-square test.
|
Up to 360 days post-PVE
|
Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Scott L. Nyberg, MD, PhD, Mayo Clinic in Rochester
Publicações e links úteis
Links úteis
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
- Neoplasias por local
- Neoplasias
- Doenças Intestinais
- Neoplasias gastrointestinais
- Neoplasias do Aparelho Digestivo
- Doenças do aparelho digestivo
- Doenças Gastrointestinais
- Neoplasias Intestinais
- Doenças retais
- Doenças do cólon
- Neoplasias Colorretais
- Técnicas de investigação
- Terapêutica
- Técnicas de laboratório clínico
- Técnicas e procedimentos de diagnóstico
- Diagnóstico
- Procedimentos cirúrgicos, operatórios
- Técnicas citológicas
- Citodiagnóstico
- Técnicas de diagnóstico, cirúrgico
- Procedimentos cirúrgicos do sistema digestivo
- Técnicas de química, analíticas
- Análise de espectro
- Técnicas hemostáticas
- Oclusão terapêutica
- Biópsia
- Manipulação de amostras
- Espectroscopia de ressonância magnética
- Hepatectomia
- Embolização, terapêutica
Outros números de identificação do estudo
- MC250412
- 25-010359 (Outro identificador: Mayo Clinic Institutional Review Board)
- R01DK140085 (Concessão/Contrato do NIH dos EUA)
Informações sobre medicamentos e dispositivos, documentos de estudo
Estuda um medicamento regulamentado pela FDA dos EUA
Estuda um produto de dispositivo regulamentado pela FDA dos EUA
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 .