FPS-ZM1 With or Without Dexamethasone for Controlling Post Operative Cerebral Edema in Patients With Glioblastoma
A Phase 1 Study of the RAGE Inhibitor FPS-ZM1 for Controlling Post-Operative Cerebral Edema in Glioblastoma Patients
調査の概要
状態
詳細な説明
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.
研究の種類
入学 (推定)
段階
- フェーズ 1
連絡先と場所
研究場所
-
-
California
-
Duarte、California、アメリカ、91010
- City of Hope Medical Center
-
主任研究者:
- Jana L. Portnow
-
コンタクト:
- Jana L. Portnow
- 電話番号:626-546-8293
- メール:jportnow@coh.org
-
-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
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)
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:非ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的: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.
|
MRIを受ける
他の名前:
CTスキャンを受ける
他の名前:
与えられた IV または PO
他の名前:
切除手術を受ける
他の名前:
Undergo blood, dialysate, intracavity fluid, and urine sample collection
他の名前:
Undergo placement of a temporary peritumoral microdialysis catheter
他の名前:
Undergo intracavity drain placement
他の名前:
Given PO
他の名前:
|
|
実験的: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.
|
MRIを受ける
他の名前:
CTスキャンを受ける
他の名前:
与えられた IV または PO
他の名前:
切除手術を受ける
他の名前:
Undergo blood, dialysate, intracavity fluid, and urine sample collection
他の名前:
Undergo placement of a temporary peritumoral microdialysis catheter
他の名前:
Undergo intracavity drain placement
他の名前:
Given PO
他の名前:
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
RAGE Antagonist FPS-ZM1 (FPS-ZM1) related adverse events
時間枠: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
時間枠:Up to 30 days post surgery
|
Assessed per CTCAE version 6.0.
|
Up to 30 days post surgery
|
二次結果の測定
結果測定 |
時間枠 |
|---|---|
|
Doses of dexamethasone taken post-operatively by study participants on dose Level 4
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
FPS-ZM1 concentrations in enhancing tumor tissue
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
FPS-ZM1 concentrations in non-enhancing tumor tissue
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
FPS-ZM1 concentrations in cerebrospinal fluid (CSF)
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
FPS-ZM1 concentrations in resection cavity fluid
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
Cytokine concentrations in brain interstitium
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
Cytokine concentrations in peripheral blood
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
Cytokine concentrations in resection cavity fluid
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
Concentrations of RAGE ligands in brain extracellular fluid
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
Concentrations of RAGE ligands in CSF
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
Concentrations of RAGE ligands in resection cavity fluid
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
Concentrations of RAGE ligands in peripheral blood
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
Expression of activating markers on tumor infiltrating lymphocytes
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
Expression of activating markers on myeloid cells
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
Expression of activating markers on lymphocytes in resection cavity fluid
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
Expression of activating markers on myeloid cells in resection cavity fluid
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
Expression of activating markers on lymphocytes in peripheral blood
時間枠:Up to 30 days
|
Up to 30 days
|
|
Expression of activating markers on myeloid cells in peripheral blood
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
T1 enhancing tumor volume from segmented T1-weighted magnetic resonance imaging (MRI)
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
Mean intratumoral perfusion from dynamic contrast enhanced (DCE)-MRI
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
Interstitial fluid flow from DCE-MRI
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
T2-FLAIR enhancing edema from segmented T2-FLAIR MRI
時間枠: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
時間枠: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
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
Mean intratumoral lactate and glutatione concentration as measured by multiplexed MR spectroscopy
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
FPS-ZM1 plasma pharmacokinetics: Maximum Observed Plasma Concentration (Cmax)
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
FPS-ZM1 plasma pharmacokinetics: Area Under the Plasma Concentration-Time Curve (AUC)
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
FPS-ZM1 plasma pharmacokinetics: Terminal Elimination Half-Life (t½)
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
|
FPS-ZM1 plasma pharmacokinetics: Clearance (CL)
時間枠:Up to 30 days post surgery
|
Up to 30 days post surgery
|
協力者と研究者
捜査官
- 主任研究者:Jana L Portnow、City of Hope Medical Center
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
- 新生物
- 組織型別の新生物
- 新生物、腺および上皮
- 星細胞腫
- 新生物、神経上皮
- 神経外胚葉性腫瘍
- 新生物、生殖細胞および胚
- 新生物、神経組織
- 膠芽腫
- 神経膠腫
- 硫黄化合物
- 有機化学物質
- 調査手法
- 臨床検査技術
- 診断技術と手順
- 診断
- 外科的処置、手術
- 炭化水素
- 炭化水素、周期的
- 炭化水素、芳香
- 多環式化合物
- 妊娠
- 妊娠
- ステロイド
- 融合リング化合物
- ステロイド、フッ素化
- ベンゼン誘導体
- 化学技術、分析
- スルホン酸
- 硫酸
- スペクトル分析
- 妊娠症
- ベンゼンスルホン酸塩
- アリルスルホン酸塩
- アリールスルホン酸
- デキサメタゾン
- ドベシル酸カルシウム
- 標本処理
- 磁気共鳴分光法
- 低侵襲外科的処置
- デキサメタゾン21-リン酸
- Auricularum
- デキサメタゾン酢酸
- FPS-ZM1
その他の研究ID番号
- 25116 (その他の識別子:City of Hope Medical Center)
- P30CA033572 (米国 NIH グラント/契約)
- U19CA264512 (米国 NIH グラント/契約)
- NCI-2026-05499 (レジストリ識別子:CTRP (Clinical Trial Reporting Program))
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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