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HRX215, A First Generation MKK4 Inhibitor Drug, for the Treatment of Patients With Colorectal Liver Metastasis After Undergoing a Portal Vein Embolization

10 juin 2026 mis à jour par: Mayo Clinic

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)

This phase IIb trial tests the effect of HRX215 in treating patients with colorectal cancer that has spread from where it first started to the liver (liver metastasis) after undergoing a portal vein embolization (PVE). Currently, surgery to remove the tumor (hepatectomy) remains the only potential treatment for cure. However, less than 30% of patients are considered resectable (can be removed by surgery) at the time of diagnosis. The risk of liver failure and other complications rise with larger areas liver that is removed during surgery. Therefore, the potential for surgery is determined by the amount of liver that will remain after resection. PVE is a standard strategy to increase the potential for resection. A PVE is a procedure that blocks the portal vein (a blood vessel that carries blood to the liver) to prevent flow of blood to the tumor. HRX215 targets and binds to MKK4, a protein found on liver cells plays a part in cellular growth and prevents liver repair and regrowth of cells and tissue. Blocking the activity of MKK4 may help prevent liver failure, protect liver cells and improve liver mass. Giving HRX215 after a PVE may help improve the rate of liver regrowth and increase the likelihood of hepatectomy in patients with colorectal liver metastasis.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Estimé)

80

Phase

  • Phase 2

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Sauvegarde des contacts de l'étude

  • Nom: Cancer Center Clinical Trials Referral Office
  • Numéro de téléphone: 507-293-6386

Lieux d'étude

    • Minnesota
      • Rochester, Minnesota, États-Unis, 55905
        • Mayo Clinic in Rochester
        • Contact:
        • Contact:
          • Cancer Center Clinical Trials Referral Office
          • Numéro de téléphone: 507-293-6386
        • Chercheur principal:
          • Scott L. Nyberg, MD, PhD

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Non

La description

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

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Tripler

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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.
Passer une IRM
Autres noms:
  • IRM
  • Résonance magnétique
  • Balayage d'imagerie par résonance magnétique
  • Imagerie Médicale, Résonance Magnétique / Résonance Magnétique Nucléaire
  • M
  • Imagerie IRM
  • Imagerie RMN
  • NMRI
  • Imagerie par résonance magnétique nucléaire
  • Imagerie par résonance magnétique (IRM)
  • IRMs
  • Imagerie par résonance magnétique (procédure)
  • IRM structurelle
Subir une collecte d'échantillons de sang
Autres noms:
  • Collecte d'échantillons biologiques
  • Spécimen biologique collecté
  • Collecte de spécimens
  • Collection d'échantillons
Subir une biopsie tissulaire
Autres noms:
  • Bx
  • BIOPSIE_TYPE
  • Biopsie
Undergo CT and CT-PET
Autres noms:
  • TDM
  • CHAT
  • Scanner
  • Tomographie axiale informatisée
  • Tomographie assistée par ordinateur
  • Tomodensitométrie
  • tomographie
  • Tomographie axiale informatisée (procédure)
  • Tomodensitométrie (TDM)
  • Scan de chat diagnostique
  • Type de service de scan de chat diagnostique
Given PO
Autres noms:
  • HRX 215
  • HRX-215
  • HRX215
  • LN 3348
  • LN-3348
  • LN3348
Undergo PVE
Autres noms:
  • Embolisation
  • therapy, embolization
Undergo hepatectomy
Autres noms:
  • Résection hépatique
Undergo CT-PET
Autres noms:
  • Imagerie médicale, Tomographie par émission de positrons
  • TEP-scan
  • Scan de tomographie par émission de positrons
  • Tomographie par émission de positrons
  • PT
  • Tomographie par émission de positrons (procédure)
  • PET (positron emission tomography)
Comparateur 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.
Passer une IRM
Autres noms:
  • IRM
  • Résonance magnétique
  • Balayage d'imagerie par résonance magnétique
  • Imagerie Médicale, Résonance Magnétique / Résonance Magnétique Nucléaire
  • M
  • Imagerie IRM
  • Imagerie RMN
  • NMRI
  • Imagerie par résonance magnétique nucléaire
  • Imagerie par résonance magnétique (IRM)
  • IRMs
  • Imagerie par résonance magnétique (procédure)
  • IRM structurelle
Subir une collecte d'échantillons de sang
Autres noms:
  • Collecte d'échantillons biologiques
  • Spécimen biologique collecté
  • Collecte de spécimens
  • Collection d'échantillons
Bon de commande donné
Subir une biopsie tissulaire
Autres noms:
  • Bx
  • BIOPSIE_TYPE
  • Biopsie
Undergo CT and CT-PET
Autres noms:
  • TDM
  • CHAT
  • Scanner
  • Tomographie axiale informatisée
  • Tomographie assistée par ordinateur
  • Tomodensitométrie
  • tomographie
  • Tomographie axiale informatisée (procédure)
  • Tomodensitométrie (TDM)
  • Scan de chat diagnostique
  • Type de service de scan de chat diagnostique
Undergo PVE
Autres noms:
  • Embolisation
  • therapy, embolization
Undergo hepatectomy
Autres noms:
  • Résection hépatique
Undergo CT-PET
Autres noms:
  • Imagerie médicale, Tomographie par émission de positrons
  • TEP-scan
  • Scan de tomographie par émission de positrons
  • Tomographie par émission de positrons
  • PT
  • Tomographie par émission de positrons (procédure)
  • PET (positron emission tomography)

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Future liver remnant size (FLR)
Délai: 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

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
FLR size
Délai: 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)
Délai: 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
Délai: 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)
Délai: 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
Délai: 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)
Délai: 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)
Délai: 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
Délai: 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

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Les enquêteurs

  • Chercheur principal: Scott L. Nyberg, MD, PhD, Mayo Clinic in Rochester

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

1 septembre 2026

Achèvement primaire (Estimé)

1 août 2028

Achèvement de l'étude (Estimé)

1 août 2028

Dates d'inscription aux études

Première soumission

21 mai 2026

Première soumission répondant aux critères de contrôle qualité

21 mai 2026

Première publication (Réel)

28 mai 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

12 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

10 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Oui

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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