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FPS-ZM1 With or Without Dexamethasone for Controlling Post Operative Cerebral Edema in Patients With Glioblastoma

25 août 2026 mis à jour par: City of Hope Medical Center

A Phase 1 Study of the RAGE Inhibitor FPS-ZM1 for Controlling Post-Operative Cerebral Edema in Glioblastoma Patients

This phase I trial tests the safety, side effects, best dose and how well FPS-ZM1 works for controlling post operative cerebral edema in patients with glioblastoma. FPS-ZM1 works by blocking the pathway that controls inflammation. Dexamethasone is in a class of medications called corticosteroids. It is used to reduce inflammation and lower the body's immune response to help lessen the side effects of chemotherapy drugs. Giving FPS-ZM1 with or without dexamethasone may be safe and/or effective in controlling post operative cerebral edema in patients with glioblastoma.

Aperçu de l'étude

Description détaillée

PRIMARY OBJECTIVE:

I. Determine the maximum feasible dose (MFD) of RAGE antagonist FPS-ZM1 (FPS-ZM1) administered peri-operatively to participants with newly diagnosed or recurrent glioblastoma.

SECONDARY OBJECTIVES:

I. Assess the ability of FPS-ZM1 to control participants' symptoms of post-operative cerebral edema when administered as monotherapy.

II. Describe the systemic pharmacokinetics and central nervous system (CNS) penetration of FPS-ZM1 based on concentrations of FPS-ZM1 in peripheral blood, cerebrospinal fluid (CSF), brain tumor tissue and resection cavity fluid (when obtainable).

III. Characterize cytokine concentrations over time in brain interstitial fluid, peripheral blood and resection cavity fluid (when obtainable) by dose level.

IV. Assess for evidence of RAGE inhibition in tumor tissue, CSF, brain interstitial fluid, resection cavity fluid (when obtainable) and peripheral blood by dose level.

V. Qualitatively and quantitatively assess changes in volume of cerebral edema on pre-operative brain magnetic resonance imaging (MRIs) and brain MRIs performed on post-operative Days 2 and 14 across dose levels.

OUTLINE: This is a dose-escalation study of FPS-ZM1 in combination with fixed-dose dexamethasone. Patients are assigned to 1 of 2 arms.

ARM I (DOSE LEVELS 1-3): Starting 2 days prior to surgery, patients receive FPS-ZM1 orally (PO) daily (QD) until post operative day 11, and dexamethasone intravenously (IV) or PO QD taper until post operative day 14, in the absence of disease progression or unacceptable toxicity. On day of surgery patients undergo standard of care resection and, if possible, undergo placement of a temporary peritumoral microdialysis catheter and intracavity drain for collection of dialysate and intracavity fluid. Patients undergo urine sample collection during screening, lumbar puncture with CSF collection and computed tomography (CT) scan on study and brain MRI, and blood sample collection throughout the study.

ARM II (DOSE LEVEL 4): Starting 2 days prior to surgery, patients receive FPS-ZM1 PO QD and, if needed for physiologic replacement, a smaller dose of dexamethasone IV or PO QD until post operative day 11, in the absence of disease progression or unacceptable toxicity. On day of surgery patients undergo standard of care resection and, if possible, undergo placement of a temporary peritumoral microdialysis catheter and intracavity drain for collection of dialysate and intracavity fluid. Patients undergo urine sample collection during screening, lumbar puncture with CSF collection and CT scan on study and brain MRI, and blood sample collection throughout the study.

After completion of study treatment, patients are followed up at day 30.

Type d'étude

Interventionnel

Inscription (Estimé)

24

Phase

  • La phase 1

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.

Lieux d'étude

    • California
      • Duarte, California, États-Unis, 91010
        • City of Hope Medical Center
        • Chercheur principal:
          • Jana L. Portnow
        • Contact:

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:

  • Documented informed consent given by the participant. Non-English speaking adults are eligible for participation if they have the capacity to understand and consent to the study procedures
  • Age: ≥ 18 years
  • Karnofsky Performance Status (KPS) ≥ 70%
  • Histologically confirmed glioblastoma or radiographic findings consistent with a high grade glioma
  • Newly diagnosed or recurrent tumor
  • The patient is planning to undergo a standard-of-care craniotomy for gross total resection of enhancing tumor
  • The patient's pre-operative brain MRI shows the presence of mild to moderate cerebral edema, defined as a midline shift of less than 10 mm
  • Dose Levels 1-3 participants: If taking more than a total of 6 mg a day of dexamethasone at the time of signing the consent form, it is anticipated by the neurosurgeon that the participant will be able to decrease their dose of dexamethasone to 6 mg daily by 4 days before the surgery (pre-operative Day -4)
  • Dose Level 4 participants: If taking more than 1 mg a day of dexamethasone at the time of signing the consent form, it is anticipated by the neurosurgeon that the participant will be able to taper their dose of dexamethasone to 1 mg daily or less by pre-operative Day -4
  • The patient is not planning to be in another clinical trial during the study period
  • The patient has recovered from any acute toxic effects (except alopecia) to ≤ grade 1 of prior anti-cancer therapy
  • No limit to prior number of therapies. The following time periods must have elapsed prior to the start of study treatment: 6 weeks from nitrosourea-containing chemotherapy, 4 weeks from non-nitrosourea-containing cytotoxic chemotherapy (except 23 days from last daily dose of temozolomide taken in a 5 of 28 day regimen, 5 half-lives from last dose of a targeted agent, and 4 weeks from the last dose of bevacizumab). There is no time period requirement for prior radiation therapy
  • Absolute neutrophil count (ANC) ≥ 1,000/mm^3
  • Platelets ≥ 100,000/mm^3
  • Hemoglobin ≥ 9g/dL
  • Total bilirubin ≤ 1.5 X upper limit of normal (ULN) (unless has Gilbert's disease)
  • Aspartate aminotransferase (AST) ≤ 1.5 x ULN
  • Alanine aminotransferase (ALT) ≤ 1.5 x ULN
  • Estimated glomerular filtration rate (eGFR) ≥ 60 mL/min
  • International Normalized Ratio (INR) OR Prothrombin (PT) ≤ 1.5 x ULN
  • Activated Partial Thromboplastin Time (aPTT) ≤ 1.5 x ULN
  • Corrected QT interval (QTc) ≤ 450 ms

    • Must have a Fridericia's corrected QT interval (QTcF) ≤ 450 msec calculated with Fridericia formula
  • Left ventricular ejection fraction (LVEF) ≥ 50%
  • People of childbearing potential who have uteri: negative urine or serum pregnancy test
  • Contraception:

    • Agreement by participants of childbearing potential or participants who are partners of people with childbearing potential to use an effective method of birth control or abstain from heterosexual activity for the course of the study through at least 3 months after the last dose of protocol therapy.

Contraception guidance (as per the information included in the informed consent document):

  • Acceptable medically effective forms of birth control are:

    • Surgical sterilization (tubal ligation or hysterectomy, or vasectomy, as applicable),
    • Double-barrier methods (i.e. condoms, diaphragm, cervical cap, or sponge used with spermicidal gel or foam),
    • Intrauterine device (IUD) (i.e. Progestin, Copper),
    • Hormonal Contraceptives (Birth control patches, implants, pills, rings, or injections)

Exclusion Criteria:

  • The patient is taking a medication that is a strong or moderate inducer or inhibitor of major CYP450 isoenzymes and drug transporters, and the patient is not able to stop that medication at least 14 days prior to start of study treatment
  • The patient has a risk factor for torsades de pointes, such as structural heart disease (history of myocardial infarction, congestive heart failure, left ventricular hypertrophy), electrolyte abnormalities (hypokalemia, hypomagnesemia), bradycardia or heart blocks, or a family history of Long QT syndrome
  • The patient is taking a medication that prolongs the QT/QTc interval and is not able to stop that medication at least 14 days prior to start of study treatment
  • The patient is unwilling to stop taking herbal medications prior to the start of study treatment
  • The patient is taking a hepatic enzyme-inducing anti-seizure medication within 14 days prior to start of study treatment
  • Patient is planning to participate in clinical trial or start a new therapy for their brain tumor during the study period: Day -2 to Day 14
  • Patient has not recovered from toxicities of prior therapy (must be grade 1 or less) except alopecia
  • Adults who lack the capacity to provide informed consent, including individuals who would require consent from a Legally Authorized Representative (LAR)
  • Clinically significant uncontrolled illness
  • Active infection requiring antibiotics
  • Participants with human immunodeficiency virus (HIV) are excluded due to concerns about inadvertent augmentation of infectious and/or inflammatory activity
  • Undergoing treatment for another cancer
  • Issues with tolerating oral medication (e.g. inability to swallow, malabsorption issues, ongoing nausea or vomiting)
  • Chronic or active viral infection of the CNS
  • Participant is pregnant or breastfeeding
  • Coagulopathy or bleeding disorder
  • Inability to undergo a brain MRI
  • Inability to tolerate dexamethasone
  • Any other condition that would, in the investigator's judgment, contraindicate participation in the clinical study due to safety concerns with clinical study procedures
  • Prospective participants who, in the opinion of the investigator, may not be able to comply with all study procedures (including compliance issues related to feasibility/logistics)

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: Non randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Arm I (FPS-ZM1 and dexamethasone)
Starting 2 days prior to surgery, patients receive FPS-ZM1 PO QD until post operative day 11, and dexamethasone IV or PO QD taper until post operative day 14, in the absence of disease progression or unacceptable toxicity. On day of surgery patients undergo standard of care resection and, if possible, undergo placement of a temporary peritumoral microdialysis catheter and intracavity drain for collection of dialysate and intracavity fluid. Patients undergo urine sample collection during screening, lumbar puncture with cerebrospinal fluid collection and CT scan on study and brain MRI, and blood sample collection throughout the 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
Passer un scanner
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
Donné IV ou PO
Autres noms:
  • Décadron
  • Hémady
  • Aacidexam
  • Adexone
  • Aknichthol Dexa
  • Alba-Dex
  • Aline
  • Alin Dépôt
  • Alin Oftalmico
  • Ampliderme
  • Anémone mono
  • Auriculaire
  • Auxiloson
  • Baycadron
  • Baycuten
  • Baycuten N
  • Cortidexason
  • Cortisumman
  • Décacort
  • Décadrol
  • Décadron DP
  • Décalix
  • Décaméth
  • Decasone R.p.
  • Dectancyl
  • Deltafluorène
  • Déronil
  • Désaméthasone
  • Désameton
  • Dexa-Mamaillet
  • Dexa-Rhinosan
  • Dexa-Scheroson
  • Dexa-sinus
  • Dexacortal
  • Dexacortine
  • Dexafarma
  • Dexafluorène
  • Dexalocal
  • Dexamecortine
  • Dexaméth
  • Dexaméthasone Intensol
  • Dexaméthasone
  • Dexamonozone
  • Dexapos
  • Dexinoral
  • Dexon
  • Dinormon
  • Dxevo
  • Fluorodelta
  • Fortecortine
  • Gammacorten
  • Hexadécarol
  • Hexadrol
  • Localison-F
  • Loverine
  • Méthylfluorprednisolone
  • Millicorten
  • Myméthasone
  • Orgadrone
  • Spersadex
  • TaperDex
  • Visumétazone
  • ZoDex
  • LénaDex
Subir une chirurgie de résection
Autres noms:
  • Résection chirurgicale
Undergo blood, dialysate, intracavity fluid, and urine sample collection
Autres noms:
  • Collecte d'échantillons biologiques
  • Spécimen biologique collecté
  • Collecte de spécimens
  • Collection d'échantillons
Undergo placement of a temporary peritumoral microdialysis catheter
Autres noms:
  • Invasive
Undergo intracavity drain placement
Autres noms:
  • Invasive
Given PO
Autres noms:
  • FPS ZM1
  • FPS-ZM1
  • FPSZM1
  • RAGE Inhibitor FPS-ZM1
Expérimental: Arm II (FPS-ZM1)
Starting 2 days prior to surgery, patients receive FPS-ZM1 PO QD and, if needed for physiologic replacement, a smaller dose of dexamethasone IV or PO QD until post operative day 11, in the absence of disease progression or unacceptable toxicity. On day of surgery patients undergo standard of care resection and, if possible, undergo placement of a temporary peritumoral microdialysis catheter and intracavity drain for collection of dialysate and intracavity fluid. Patients undergo urine sample collection during screening, lumbar puncture with cerebrospinal fluid collection and CT scan on study and brain MRI, and blood sample collection throughout the 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
Passer un scanner
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
Donné IV ou PO
Autres noms:
  • Décadron
  • Hémady
  • Aacidexam
  • Adexone
  • Aknichthol Dexa
  • Alba-Dex
  • Aline
  • Alin Dépôt
  • Alin Oftalmico
  • Ampliderme
  • Anémone mono
  • Auriculaire
  • Auxiloson
  • Baycadron
  • Baycuten
  • Baycuten N
  • Cortidexason
  • Cortisumman
  • Décacort
  • Décadrol
  • Décadron DP
  • Décalix
  • Décaméth
  • Decasone R.p.
  • Dectancyl
  • Deltafluorène
  • Déronil
  • Désaméthasone
  • Désameton
  • Dexa-Mamaillet
  • Dexa-Rhinosan
  • Dexa-Scheroson
  • Dexa-sinus
  • Dexacortal
  • Dexacortine
  • Dexafarma
  • Dexafluorène
  • Dexalocal
  • Dexamecortine
  • Dexaméth
  • Dexaméthasone Intensol
  • Dexaméthasone
  • Dexamonozone
  • Dexapos
  • Dexinoral
  • Dexon
  • Dinormon
  • Dxevo
  • Fluorodelta
  • Fortecortine
  • Gammacorten
  • Hexadécarol
  • Hexadrol
  • Localison-F
  • Loverine
  • Méthylfluorprednisolone
  • Millicorten
  • Myméthasone
  • Orgadrone
  • Spersadex
  • TaperDex
  • Visumétazone
  • ZoDex
  • LénaDex
Subir une chirurgie de résection
Autres noms:
  • Résection chirurgicale
Undergo blood, dialysate, intracavity fluid, and urine sample collection
Autres noms:
  • Collecte d'échantillons biologiques
  • Spécimen biologique collecté
  • Collecte de spécimens
  • Collection d'échantillons
Undergo placement of a temporary peritumoral microdialysis catheter
Autres noms:
  • Invasive
Undergo intracavity drain placement
Autres noms:
  • Invasive
Given PO
Autres noms:
  • FPS ZM1
  • FPS-ZM1
  • FPSZM1
  • RAGE Inhibitor FPS-ZM1

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
RAGE Antagonist FPS-ZM1 (FPS-ZM1) related adverse events
Délai: Up to 30 days post surgery
Assessed per Common Terminology Criteria for Adverse Events (CTCAE) version 6.0.
Up to 30 days post surgery
Dose limiting toxicity rate
Délai: Up to 30 days post surgery
Assessed per CTCAE version 6.0.
Up to 30 days post surgery

Mesures de résultats secondaires

Mesure des résultats
Délai
Doses of dexamethasone taken post-operatively by study participants on dose Level 4
Délai: Up to 30 days post surgery
Up to 30 days post surgery
FPS-ZM1 concentrations in enhancing tumor tissue
Délai: Up to 30 days post surgery
Up to 30 days post surgery
FPS-ZM1 concentrations in non-enhancing tumor tissue
Délai: Up to 30 days post surgery
Up to 30 days post surgery
FPS-ZM1 concentrations in cerebrospinal fluid (CSF)
Délai: Up to 30 days post surgery
Up to 30 days post surgery
FPS-ZM1 concentrations in resection cavity fluid
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Cytokine concentrations in brain interstitium
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Cytokine concentrations in peripheral blood
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Cytokine concentrations in resection cavity fluid
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Concentrations of RAGE ligands in brain extracellular fluid
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Concentrations of RAGE ligands in CSF
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Concentrations of RAGE ligands in resection cavity fluid
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Concentrations of RAGE ligands in peripheral blood
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Expression of activating markers on tumor infiltrating lymphocytes
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Expression of activating markers on myeloid cells
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Expression of activating markers on lymphocytes in resection cavity fluid
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Expression of activating markers on myeloid cells in resection cavity fluid
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Expression of activating markers on lymphocytes in peripheral blood
Délai: Up to 30 days
Up to 30 days
Expression of activating markers on myeloid cells in peripheral blood
Délai: Up to 30 days post surgery
Up to 30 days post surgery
T1 enhancing tumor volume from segmented T1-weighted magnetic resonance imaging (MRI)
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Mean intratumoral perfusion from dynamic contrast enhanced (DCE)-MRI
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Interstitial fluid flow from DCE-MRI
Délai: Up to 30 days post surgery
Up to 30 days post surgery
T2-FLAIR enhancing edema from segmented T2-FLAIR MRI
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Mean intratumoral blood volume from relative cerebral blood volume as calculated from DSC-MRI
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Mean intratumoral tissue density as measured by the apparent diffusion coefficient derived from diffusion-weighted MRI
Délai: Up to 30 days post surgery
Up to 30 days post surgery
Mean intratumoral lactate and glutatione concentration as measured by multiplexed MR spectroscopy
Délai: Up to 30 days post surgery
Up to 30 days post surgery
FPS-ZM1 plasma pharmacokinetics: Maximum Observed Plasma Concentration (Cmax)
Délai: Up to 30 days post surgery
Up to 30 days post surgery
FPS-ZM1 plasma pharmacokinetics: Area Under the Plasma Concentration-Time Curve (AUC)
Délai: Up to 30 days post surgery
Up to 30 days post surgery
FPS-ZM1 plasma pharmacokinetics: Terminal Elimination Half-Life (t½)
Délai: Up to 30 days post surgery
Up to 30 days post surgery
FPS-ZM1 plasma pharmacokinetics: Clearance (CL)
Délai: Up to 30 days post surgery
Up to 30 days post surgery

Collaborateurs et enquêteurs

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

Les enquêteurs

  • Chercheur principal: Jana L Portnow, City of Hope Medical Center

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)

17 février 2027

Achèvement primaire (Estimé)

28 août 2028

Achèvement de l'étude (Estimé)

28 août 2028

Dates d'inscription aux études

Première soumission

6 août 2026

Première soumission répondant aux critères de contrôle qualité

25 août 2026

Première publication (Réel)

27 août 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

27 août 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

25 août 2026

Dernière vérification

1 août 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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