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Zanzalintinib and MO-03 for the Treatment of Metastatic Renal Cell Cancer After Progression on Immunotherapy

2026年5月5日 更新者:City of Hope Medical Center

Phase 2, Single-Arm Trial of Zanzalintinib (XL092) With MO-03 (CBM588 Capsule) in Patients With Metastatic Renal Cell Carcinoma (mRCC) After Progression to Immunotherapy

This phase II trial tests how well zanzalintinib and MO-03 works for the treatment of renal cell cancer that has spread from where it first started (primary site) to other places in the body (metastatic) and that is growing, spreading, or getting worse (progression) after receiving immunotherapy. Zanzalintinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. MO-03 is a type of medication called a microbiome-based immunomodulator. It helps control some of the bacteria found in the gut which may make the zanzalintinib more effective. Giving zanzalintinib with MO-03 may be effective for treating metastatic renal cell cancer after progression on immunotherapy.

調査の概要

詳細な説明

PRIMARY OBJECTIVE:

I. To evaluate the anti-tumor efficacy of zanzalintinib (XL092) in combination with C. butyricum CBM 588 Probiotic Strain Capsule Formulation MO-03 (MO-03) in patients with metastatic renal cell carcinoma (mRCC) at second line or third line after disease progression to both a checkpoint inhibitor and cabozantinib, as measured by the objective response rate (ORR) using Response Evaluation Criteria in Solid Tumors (RECIST) version (v) 1.1 criteria.

SECONDARY OBJECTIVES:

I. To assess changes in the gut microbiome composition from baseline to week 12, to understand the impact of CBM588 with XL092 on microbiome modulation.

II. To evaluate microbial diversity changes by comparing the Shannon index from baseline to week 12 with MO-03 and XL092, to explore any association between microbial diversity and treatment response.

III. To examine immune modulation, specifically by measuring changes in the proportion of circulating regulatory T cells (Tregs) and myeloid-derived suppressor cells (MDSCs) with the combination of XL092 and MO-03.

IV. To assess cytokine and chemokine levels at various points during the study to evaluate the immunologic response associated with XL092 and MO-03.

V. To evaluate the safety and tolerability of the XL092 and MO-03 combination, focusing on treatment-related toxicities such as diarrhea and nausea, and analyzing all adverse events and serious adverse events per Common Terminology Criteria for Adverse Events (CTCAE) v 6.0.

VI. To analyze survival outcomes, specifically progression-free survival (PFS) and overall survival (OS), using Kaplan-Meier estimates to determine time-to-event distributions and provide an early indication of clinical benefit.

EXPLORATORY OBJECTIVES:

I. To assess the changes in metabolic pathways within the gut microbiome over the course of treatment with XL092 and MO-03.

II. To evaluate the changes in fungal microbiome profiles in response to treatment with XL092 and MO-03.

OUTLINE:

Patients receive XL092 orally (PO) once daily (QD) and MO-03 PO twice daily (BID) on days 1-28 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Study treatment may continue after progression if the Investigator believes that the subject is still receiving clinical benefit. Patients undergo computed tomography (CT) scan, bone scan, and blood and urine sample collection throughout the study.

After completion of study treatment, patients are followed up at 30 days and every 12 weeks for 2 years.

研究の種類

介入

入学 (推定)

34

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • California
      • Duarte、California、アメリカ、91010
        • City of Hope Medical Center
        • コンタクト:
          • Sumanta K. Pal
          • 電話番号:626-256-4673
          • メール:spal@coh.org
        • 主任研究者:
          • Sumanta K. Pal

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

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

いいえ

説明

Inclusion Criteria:

  • Capable of understanding and complying with the protocol requirements and must have signed the informed consent document
  • Agreement to allow the use of archival tissue from diagnostic tumor biopsies

    • If unavailable, exceptions may be granted with study principal investigator (PI) approval
  • Age: ≥ 18 years
  • Gender: Males and females are eligible
  • Any ethnicity or race
  • Eastern Cooperative Oncology Group (ECOG) ≤ 2
  • Histologically confirmed renal cell carcinoma with a clear-cell histology
  • Patients must have received one or two prior lines of systemic therapy for metastatic disease, which must include prior treatment with a checkpoint inhibitor and cabozantinib (not necessarily in the same line). Prior use of hypoxia-inducible factor (HIF) inhibitors or other tyrosine kinase inhibitors (TKIs) other than cabozantinib are not allowed
  • Measurable metastatic disease by RECIST v 1.1 criteria
  • Recovery to baseline or ≤ grade 1 severity (CTCAE v 6.0) from adverse events (AEs), including immune-related adverse events (irAEs), related to any prior treatments, unless AE(s) are clinically nonsignificant and/or stable on supportive therapy (e.g., physiological replacement of corticosteroid). Low-grade or controlled toxicities such as alopecia, ≤ grade 2 hypomagnesemia, ≤ grade 2 neuropathy are permitted)
  • White blood cell (WBC) > 2,000/mm^3 (to be performed within 14 days prior to day 1 of protocol therapy unless otherwise stated)

    • NOTE: Growth factor is not permitted within 14 days of absolute neutrophil count (ANC) assessment unless cytopenia is secondary to disease involvement
  • Neutrophils ≥ 1,500/mm^3 (to be performed within 14 days prior to day 1 of protocol therapy unless otherwise stated)

    • NOTE: Growth factor is not permitted within 14 days of absolute neutrophil count (ANC) assessment unless cytopenia is secondary to disease involvement
  • Platelets ≥ 100,000/mm^3 (to be performed within 14 days prior to day 1 of protocol therapy unless otherwise stated)

    • NOTE: Platelet transfusions are not permitted within 14 days of platelet assessment unless cytopenia is secondary to disease involvement
  • Hemoglobin ≥ 9g/dL (to be performed within 14 days prior to day 1 of protocol therapy unless otherwise stated)

    • NOTE: Red blood cell transfusions are not permitted within 14 days of hemoglobin assessment unless cytopenia is secondary to disease involvement
  • Total bilirubin ≤ 1.5 X upper limit of normal (ULN) (except for subjects with Gilbert Syndrome, who may have total bilirubin up to 3.0 mg/dL) (to be performed within 14 days prior to day 1 of protocol therapy unless otherwise stated)
  • Aspartate aminotransferase (AST) ≤ 3.0 x ULN (except for subjects with Gilbert Syndrome, who may have total bilirubin up to 3.0 mg/dL) (to be performed within 14 days prior to day 1 of protocol therapy unless otherwise stated)
  • Alkaline phosphatase (ALP) ≤ 3.0 x ULN. For subjects with documented bone metastasis ALP ≤ 5 x ULN (to be performed within 14 days prior to day 1 of protocol therapy unless otherwise stated)
  • Creatinine clearance ≥ 40 mL/min the Cockcroft-Gault formula (to be performed within 14 days prior to day 1 of protocol therapy unless otherwise stated)
  • If not receiving anticoagulants: International normalized ratio (INR) OR prothrombin (PT) ≤ 1.5 x ULN. If on anticoagulant therapy: PT must be within therapeutic range of intended use of anticoagulants (to be performed within 14 days prior to day 1 of protocol therapy unless otherwise stated)
  • If not receiving anticoagulants: Activated partial thromboplastin time (aPTT) ≤ 1.2 x ULN, INR ≤ 1.5. If on anticoagulant therapy: aPTT must be within therapeutic range of intended use of anticoagulants (to be performed within 14 days prior to day 1 of protocol therapy unless otherwise stated)
  • QT interval corrected by Bazett's formula (QTcB) ≤ 480 ms

    • Note: To be performed within 28 days prior to day 1 of protocol therapy
  • If seropositive for HIV, hepatitis C virus (HCV) or hepatitis B virus (HBV), nucleic acid quantitation must be performed. Viral load must be undetectable. HIV-infected, chronic carriers of HBV, and chronic carriers of HCV on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial
  • Meets other institutional and federal requirements for infectious disease titer requirements

    • Note: Infectious disease testing to be performed within 28 days prior to day 1 of protocol therapy
  • Women of childbearing potential (WOCBP): negative urine or serum pregnancy test. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required
  • Sexually active fertile subjects and their partners must agree to use highly effective method of contraception during the course of the study and for the following durations after the last dose of treatment (whichever is later). An additional contraceptive method, such as a barrier method (e.g., condom), is required. In addition, men must agree not to donate sperm and women must agree not to donate eggs (ova, oocyte) for the purpose of reproduction during these same periods, through 186 days after the last dose of zanzalintinib for women of childbearing potential (WOCBP) or through 96 days after the last dose of zanzalintinib for men
  • Female subjects of childbearing potential must not be pregnant at screening. Female subjects are considered to be of childbearing potential unless one of the following criteria is met: permanent sterilization (hysterectomy, bilateral salpingectomy, or bilateral oophorectomy) or documented postmenopausal status (defined as 12 months of amenorrhea in a woman > 45 years-of-age in the absence of other biological or physiological causes. In addition, females < 55 years-of-age must have a serum follicle stimulating hormone [FSH] level > 40 mIU/mL to confirm menopause).

    • Note: Documentation may include review of medical records, medical examination, or medical history interview by study site staff

Exclusion Criteria:

  • Prior treatment with zanzalintinib
  • Receipt of any type of cytotoxic, biologic or other systemic anticancer therapy (including investigational) within 4 weeks before first dose of study treatment
  • Radiation therapy for bone metastasis within 2 weeks, any other radiation therapy within 4 weeks before first dose of study treatment. Systemic treatment with radionuclides within 6 weeks before first dose of study treatment. Subjects with clinically relevant ongoing complications from prior radiation therapy are not eligible
  • Known brain metastases or cranial epidural disease unless adequately treated with radiotherapy and/or surgery (including radiosurgery) and stable for at least 4 weeks before first dose of study treatment

    • Note: Eligible subjects must be neurologically asymptomatic and without corticosteroid treatment at the time of enrollment.
    • Note: Base of skull lesions without definitive evidence of dural or brain parenchymal involvement are allowed
  • Known medical condition (e.g., chronic diarrhea or acute diverticulitis) that, in the investigator's opinion, would increase the risk associated with study participation or study drug administration or interfere with the interpretation of safety results
  • Concomitant anticoagulation with oral anticoagulants (e.g., warfarin, direct thrombin inhibitors ) and platelet inhibitors (e.g., clopidogrel).Allowed anticoagulants are the following:

    • Prophylactic use of low-dose aspirin for cardio-protection (per local applicable guidelines) and low-dose low molecular weight heparins (LMWH).
    • Therapeutic doses of LMWH or anticoagulation with direct factor Xa inhibitors rivaroxaban, edoxaban, or apixaban in subjects without known brain metastases who are on a stable dose of the anticoagulant for at least 1 week before first dose of study treatment without clinically significant hemorrhagic complications from the anticoagulation regimen.

      • Note: Subjects must have discontinued oral anticoagulants within 3 days or 5 half-lives prior to first dose of study treatment, whichever is longer
  • Any complementary medications (e.g., herbal supplements or traditional Chinese medicines) to treat the disease under study within 2 weeks before first dose of study treatment
  • The subject has uncontrolled, significant intercurrent or recent illness including, but not limited to, the following conditions:

    • Unstable or deteriorating cardiovascular disorders:

      • Congestive heart failure New York Heart Association Class 3 or 4, class 2 or higher, unstable angina pectoris, new-onset angina, serious cardiac arrhythmias (e.g., ventricular flutter, ventricular fibrillation, Torsades de pointes).
      • Uncontrolled hypertension defined as sustained blood pressure (BP) > 140 mm Hg systolic or > 90 mm Hg diastolic despite optimal antihypertensive treatment.
      • Stroke (including transient ischemic attack [TIA]), myocardial infarction, or other clinically significant arterial thrombotic and/or ischemic event within 6 months before first dose of study treatment.
      • Pulmonary embolism (PE) or deep vein thrombosis (DVT) or prior clinically significant venous events within 3 months before first dose of study treatment.

        • Note: Subjects with a diagnosis of DVT within 6 months are allowed if asymptomatic and stable at screening and are on a stable dose of the anticoagulant for at least 1 week before first dose of study treatment without clinically significant hemorrhagic complications from the anticoagulation regimen.
        • Note: Subjects who don't require prior anticoagulation therapy may be eligible but must be discussed and approved by the Principal Investigator
  • Prior history of myocarditis.

    • Gastrointestinal (GI) disorders including those associated with a high risk of perforation or fistula formation:

      • Tumors invading the GI-tract from external viscera.
      • Active peptic ulcer disease, inflammatory bowel disease, diverticulitis, cholecystitis, symptomatic cholangitis or appendicitis, or acute pancreatitis.
      • Acute obstruction of the bowel, gastric outlet, or pancreatic or biliary duct within 6 months before first dose unless cause of obstruction is definitively managed and subject is asymptomatic.
      • Abdominal fistula, gastrointestinal perforation, bowel obstruction, or intra-abdominal abscess within 6 months before first dose.

        • Note: Complete healing of an intra-abdominal abscess must be confirmed before first dose of study treatment
  • Known gastric or esophageal varices
  • Ascites, pleural effusion, or pericardial fluid requiring drainage in last 4 weeks
  • Clinically significant hematuria, hematemesis, or hemoptysis of > 0.5 teaspoon (2.5 ml) of red blood, or other history of significant bleeding (e.g., pulmonary hemorrhage) within 12 weeks before first dose of study treatment
  • Symptomatic cavitating pulmonary lesion(s) or endobronchial disease (asymptomatic or radiated lesions allowed)
  • Lesions invading major blood vessel including, but not limited to, inferior vena cava, pulmonary artery, or aorta.

    • Note: Subjects with intravascular tumor extension (e.g., tumor thrombus in renal vein or inferior V. cava) may be eligible following Principal Investigator approval
  • Other clinically significant disorders that would preclude safe study participation

    • Active infection requiring systemic treatment. Note: Prophylactic antimicrobial treatments (antibiotics, antimycotic, antiviral) are allowed.
    • Known infection with acute or chronic hepatitis B or C, known human immunodeficiency virus (HIV) or acquired immunodeficiency syndrome (AIDS)-related illness except for subjects meeting all of the following criteria:

      • (1) Chronic carriers of HBV infection (hepatitis B surface antigen [HBsAg]-positive, anti-hepatitis B core antibody [anti-HBc]-positive) who have undetectable HBV deoxyribonucleic acid (DNA) and are on stable suppressive antiviral therapy.
      • (2) Individuals with prior HCV infection who have completed curative antiviral treatment and achieved undetectable HCV viral load.
      • (3) Chronic carriers of HCV infection who are on stable suppressive antiviral therapy and have undetectable HCV viral load.
      • (4) HIV-infected patients on stable anti-retroviral therapy with CD4+ T cell count ≥ 200/µL; and) an undetectable viral load. *** Note: HIV testing will be performed at screening if and as required by local regulation.

        • Note: To be eligible, participants taking CYP inhibitors (e.g., zidovudine, ritonavir, cobicistat, didanosine) or CYP3 inducers (efavirenz) must change to a different regimen not including these drugs 7 days prior to initiation of study treatment. Anti-retroviral therapies (ART) must have been received for at least 4 weeks prior to the first dose.
        • Note: CD4+ T cell counts, and viral load are monitored per standard of care by the local health care provider.
    • Serious non-healing wound/ulcer/bone fracture.

      • Note: non-healing wounds or ulcers are permitted if due to tumor-associated skin lesions.
    • Malabsorption syndrome.
    • Pharmacologically uncompensated, symptomatic hypothyroidism.
    • Moderate to severe hepatic impairment (Child-Pugh B or C).
    • Requirement for hemodialysis or peritoneal dialysis.
    • History of solid organ or allogeneic stem cell transplant
  • Major surgery (e.g., GI surgery, removal or biopsy of brain metastasis) within 8 weeks prior to first dose of study treatment. Prior laparoscopic surgeries (i.e. nephrectomy) within 4 weeks prior to first dose of study treatment. Minor surgery (e.g., simple excision, tooth extraction) within 5 days before first dose of study treatment. Complete wound healing from major or minor surgery must have occurred at least prior to first dose of study treatment

    • Note: Fresh tumor biopsies should be performed at least 5 days before the first dose of study treatment. Subjects with clinically relevant ongoing complications from prior surgical procedures, including biopsies, are not eligible
  • Corrected QT interval calculated by the Fridericia formula (QTcF) > 480 ms within 14 days per electrocardiogram (ECG) before first dose of study treatment.

    • Note: Triplicate ECG evaluations will be performed and the average of these 3 consecutive results for QTcF will be used to determine eligibility
  • History of psychiatric illness likely to interfere with ability to comply with protocol requirements or give informed consent
  • Women who are pregnant or breastfeeding
  • Inability to swallow tablets or ingest a suspension either orally or by a nasogastric (NG) or gastrostomy (PEG) tube
  • Previously identified allergy or hypersensitivity to components of the study treatment formulations
  • Another malignancy that requires active therapy and in the opinion of the Investigator would interfere with monitoring of radiologic assessments of response to Investigational Product, within 2 years before first dose of study treatment, except for superficial skin cancers, or localized, low-grade tumors deemed cured and not treated with systemic therapy. Incidentally diagnosed prostate cancer is allowed if assessed as stage ≤ T2N0M0 and Gleason score ≤ 6
  • Other conditions, which in the opinion of the Investigator, would compromise the safety of the patient or the patient's ability to complete the study
  • 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

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

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:なし
  • 介入モデル:単一グループの割り当て
  • 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:Treatment (zanzalintinib and MO-03)
Patients receive XL092 PO QD and MO-03 PO BID on days 1-28 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Study treatment may continue after progression if the Investigator believes that the subject is still receiving clinical benefit. Patients undergo CT scan, bone scan, and blood and urine sample collection throughout the study.
CTスキャンを受ける
他の名前:
  • CT
  • 猫
  • CATスキャン
  • コンピューター断層撮影
  • コンピュータ化されたアキシャルトモグラフィー
  • CTスキャン
  • トモグラフィー
  • コンピューター断層撮影 (手順)
  • コンピューター断層撮影 (CT) スキャン
  • 診断CATスキャン
  • 診断CATスキャンサービスタイプ
血液と尿のサンプル採取を受ける
他の名前:
  • 生物学的サンプルの収集
  • 採取された生体試料
  • 標本収集
骨スキャンを受ける
他の名前:
  • 骨シンチグラフィー
与えられたPO
他の名前:
  • XL092
  • マルチキナーゼ阻害剤 XL092
  • XL-092
Given PO
他の名前:
  • CBM588 Capsule Formulation MO-03
  • CBM588 Capsule MO-03
  • Clostridium butyricum CBM 588 Probiotic Strain Capsule Formulation MO-03
  • Clostridium butyricum CBM 588 Probiotic Strain Capule MO-03
  • Clostridium butyricum MIYAIRI 588 Capsule Formulation MO-03
  • MO 03
  • MO-03
  • MO03

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
Overall response rate
時間枠:Up to 2 years
Will be calculated as the number of patients with complete or partial response (per Response Evaluation Criteria in Solid Tumors version 1.1) divided by the total number of treated/evaluable subjects.
Up to 2 years

二次結果の測定

結果測定
メジャーの説明
時間枠
Change in gut microbiota composition in stool
時間枠:From baseline to week 12
Assessed using the proportion of Bifidobacterium spp.
From baseline to week 12
Microbial diversity
時間枠:From baseline to week 12
Assessed via comparison of the Shannon index.
From baseline to week 12
Proportion of circulating regulatory T cells
時間枠:At baseline, week 9, 13, 17 and 25
Will be assessed graphically across serial timepoints of blood collection to ascertain any trends.
At baseline, week 9, 13, 17 and 25
Proportion of circulating myeloid-derived suppressor cells
時間枠:At baseline, week 9, 13, 17 and 25
Will be assessed graphically across serial timepoints of blood collection to ascertain any trends.
At baseline, week 9, 13, 17 and 25
Cytokine levels
時間枠:At baseline, week 9, 13, 17 and 25
Will be assessed graphically across serial timepoints of blood collection to ascertain any trends.
At baseline, week 9, 13, 17 and 25
Chemokine levels
時間枠:At baseline, week 9, 13, 17 and 25
Will be assessed graphically across serial timepoints of blood collection to ascertain any trends.
At baseline, week 9, 13, 17 and 25
Treatment related toxicities
時間枠:From baseline, up to 2 years
Assessed using Common Terminology Criteria for Adverse Events (CTCAE) version (v) 6.0.
From baseline, up to 2 years
Incidence of adverse events
時間枠:Up to 2 years
Assessed using CTCAE v 6.0.
Up to 2 years
Incidence of serious adverse events
時間枠:Up to 2 years
Assessed using CTCAE v 6.0.
Up to 2 years
Progression free survival
時間枠:From start of treatment to time of progression or death, up to 2 years
Estimated using the Kaplan-Meier method with 80% confidence bands.
From start of treatment to time of progression or death, up to 2 years
Overall survival
時間枠:From start of treatment to death from any cause, up to 2 years
Estimated using the Kaplan-Meier method with 80% confidence bands.
From start of treatment to death from any cause, up to 2 years

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Sumanta K Pal、City of Hope Medical Center

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年11月28日

一次修了 (推定)

2028年6月24日

研究の完了 (推定)

2028年6月24日

試験登録日

最初に提出

2026年5月5日

QC基準を満たした最初の提出物

2026年5月5日

最初の投稿 (実際)

2026年5月11日

学習記録の更新

投稿された最後の更新 (実際)

2026年5月11日

QC基準を満たした最後の更新が送信されました

2026年5月5日

最終確認日

2026年5月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • 24926 (その他の識別子:City of Hope Comprehensive Cancer Center)
  • P30CA033572 (米国 NIH グラント/契約)
  • NCI-2026-02916 (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

はい

米国FDA規制機器製品の研究

いいえ

米国で製造され、米国から輸出された製品。

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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