[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"advanced-renal-cell-carcinoma-arcc\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:advanced-renal-cell-carcinoma-arcc":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,41],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":5},"100607464","phase-2-a-randomized-trial-of-fianlimab-and-cemiplimab---ipilimumab-or-ipilimumab-plus-nivolumab-in-first-line-advanced-renal-cell-carcinoma-rcc-100607464",false,"NCT07188896","A Randomized Trial of Fianlimab and Cemiplimab +\u002F- Ipilimumab or Ipilimumab Plus Nivolumab in First-line Advanced Renal Cell Carcinoma (RCC)","A Randomized Phase 2 Trial of Fianlimab and Cemiplimab +\u002F- Ipilimumab or Ipilimumab Plus Nivolumab in First-line Advanced Renal Cell Carcinoma (RCC)","Inclusion Criteria:\n\n1. Signed informed consent and HIPAA authorization for release of personal health information prior to registration. NOTE: HIPAA authorization may be included in the informed consent or obtained separately.\n2. Age ≥ 18 years at the time of consent.\n3. Karnofsky Performance Status ≥ 70% within 14 days prior to registration.\n4. Histological or cytological evidence of renal cell carcinoma having a clear cell component\n5. Advanced (not amenable to curative surgery or radiation therapy) or metastatic (AJCC Stage IV \\[version 9\\]) renal cell carcinoma.\n6. Treatment naïve for systemic therapy for renal cell carcinoma including no prior neo\u002Fadjuvant systemic therapy\n7. Measurable disease according to RECIST 1.1 within 28 days prior to registration.\n8. Patient must have either a formalin-fixed, paraffin-embedded (FFPE) tissue block or unstained tumor tissue sections, obtained from preferably a metastatic lesion, preferably within 3 months or no more than 12 months with an associated pathology report. If the metastatic lesion biopsy specimen does not contain at least 20 unstained slides, supplementation with primary kidney cancer tissue is acceptable.\n9. Demonstrate adequate organ function as defined in the protocol. All screening labs to be obtained within 14 days prior to registration.\n10. Females of childbearing potential must have a negative serum pregnancy test within 14 days prior to registration.\n11. Females of childbearing potential who are sexually active with a male able to father a child must be willing to abstain from penile-vaginal intercourse or must use an effective method(s) of contraception. Males able to father a child who are sexually active with a female of childbearing potential must be willing to abstain from penile-vaginal intercourse or use an effective method(s) of contraception.\n12. Known HIV-infected subjects on effective anti-retroviral therapy with undetectable viral load and CD4 count above 350 either spontaneously or on a stable antiviral regimen within 6 months of registration are eligible for this trial. Testing is not required at screening unless mandated by local policy\n13. Subjects with known chronic hepatitis B virus (HBV) infection, must have an undetectable HBV viral load (serum hepatitis B virus DNA PCR that is below the limit of detection) and be on suppressive therapy, if indicated.\n14. Subjects with a history of hepatitis C virus (HCV) infection must have been treated and cured (undetectable HCV RNA by PCR either spontaneously or in response to a successful prior course of anti-HCV therapy). For subjects with HCV infection who are currently on treatment, the HCV viral load must be undetectable to be eligible for this trial. Testing is not required at screening unless mandated by local policy.\n15. As determined by the enrolling physician or protocol designee, ability of the subject to understand and comply with study procedures for the entire length of the study.\n\nExclusion Criteria:\n\n1. Prior systemic therapy against renal cell carcinoma in the neo\u002Fadjuvant or metastatic setting\n2. Any condition requiring ongoing ≥ 10 mg prednisone equivalent\u002Fday\n3. Participants with a history of myocarditis.\n4. If clinically indicated based on clinical assessment and any ECG abnormalities, optional troponin T (TnT) or troponin I (TnI) may be done as described in the protocol.\n5. Ongoing or recent (within 2 years) evidence of an autoimmune disease that required systemic treatment with immunosuppressive agents. The following are allowed: vitiligo, childhood asthma that has resolved, residual hypothyroidism that requires only hormone replacement, psoriasis not requiring systemic treatment.\n6. Central nervous system (CNS) metastases as described in the protocol.\n7. Active infection requiring systemic therapy as described in the protocol.\n8. Pregnant or breastfeeding as described in the protocol.\n9. Prior or concurrent malignancy whose natural history or treatment has the potential to interfere with the safety or efficacy assessment of the investigational regimen, per treating physician discretion.\n10. Subjects must not receive live attenuated vaccines within 4 weeks prior to Cycle 1 Day 1 or at any time during the study. Inactivated vaccines are allowed.\n11. Known hypersensitivity to the active substances or to any of the excipients.\n12. Currently participating in another study or participated in any study of an investigational agent or investigational device within 30 days of the first dose of study drug.","ALL","18 Years",{"count":19,"type":20},120,"ESTIMATED","INTERVENTIONAL",[23],"PHASE2","This three-arm randomized phase 2 trial will enroll advanced clear cell RCC patients (all IMDC risk groups). Patients will be randomized 2:2:1 to either Arm A (fianlimab\u002F cemiplimab\u002F ipilimumab), Arm B (fianlimab\u002F cemiplimab), or Arm C (standard ipilimumab\u002F nivolumab), respectively.",[26,27,28],"Advanced Renal Cell Carcinoma (aRCC)","Metastatic Renal Cell Carcinoma ( mRCC)","Clear Cell Renal Cell Carcinoma (ccRCC)","RECRUITING","2026-07-01",{"date":32,"type":33},"2026-07-02","ACTUAL",{"date":35,"type":33},"2026-04-29",{"date":37,"type":20},"2030-11-30",{"name":39,"class":40},"Brian Rini","OTHER",{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":48,"enrollmentInfo":49,"targetDuration":4,"studyType":21,"phases":51,"briefSummary":52,"conditions":53,"keywords":4,"overallStatus":54,"whyStopped":4,"lastUpdateSubmitDate":55,"lastUpdatePostDateStruct":56,"startDateStruct":58,"completionDateStruct":60,"leadSponsor":62,"locationsCount":4},"100605182","phase-2-envafolimab-combined-with-axitinib-as-first-line-treatment-for-patients-with-advanced-renal-cell-carcinoma-100605182","NCT07159191","Envafolimab Combined With Axitinib as First-Line Treatment for Patients With Advanced Renal Cell Carcinoma","This is a Single-center, Single-arm, Phase II, Prospective Clinical Study Planning to Enroll 30 Patients With Advanced Renal Cell Carcinoma. Eligible Patients, After Signing the Informed Consent Form and Passing the Screening Process, Will Receive Envafolimab + Axitinib Treatment Until Disease Progression or Intolerable Toxicity (Treatment Duration Not Exceeding 24 Months). Clinical Tumor Imaging Assessments Will be Conducted Every 12 Weeks During the Treatment Process According to the RECIST V1.1 Criteria. Safety Will be Assessed Using CTCAE 5.0, With Adverse Events Recorded From Each Treatme","Inclusion Criteria:\n\n* 1\\. Sign an informed consent form in writing; 2. Age between 18 and 75 years old; 3. Unresectable or metastatic clear cell renal cell carcinoma; 4. No prior systemic anti-tumor treatment; 5. Measurable disease according to RECIST v1.1; 6. ECOG performance status: 0 to 1; 7. Adequate organ and bone marrow function:\n\n  1. Complete blood count: Absolute Neutrophil Count (ANC) ≥ 1.5 × 10\\^9\u002FL, Platelet (PLT) count ≥ 70 × 10\\^9\u002FL, Hemoglobin (HGB) ≥ 90 g\u002FL;\n  2. Liver function: Total Bilirubin (TBIL) ≤ 1.5 × Upper Limit of Normal Value (ULN); Alanine Aminotransferase (ALT) and Aspartate Transferase (AST) ≤ 3 × ULN; Serum Albumin ≥ 28 g\u002FL; Alkaline Phosphatase (ALP) ≤ 5 × ULN; subjects who meet the above criteria after routine liver protection treatment and have been stable for at least one week after assessment by the researcher can be enrolled;\n  3. Renal function: Serum Creatinine (Cr) ≤ 1.5 × ULN, or Creatinine Clearance ≥ 50 mL\u002Fmin (using the standard Cockcroft-Gault formula);\n  4. Coagulation function: International Normalized Ratio (INR) ≤ 1.5 \u002F Prothrombin Time (PT) ≤ 1.5 × ULN, Activated Partial Thromboplastin Time (aPTT) ≤ 1.5 × ULN; if the subject is undergoing anticoagulant therapy, as long as PT and INR are within the range specified for the anticoagulant medication, they are eligible.\n\n  8\\. Estimated life expectancy ≥ 6 months; 9. Subjects voluntarily participate in this study and have good compliance.\n\nExclusion Criteria:\n\n* 1\\. A history of or concurrent with other malignant tumors; 2. Patients who have previously received systemic anti-tumor treatment; 3. Known allergies to macromolecular protein preparations or components of the study medication in the subject's history; 4. Active autoimmune diseases requiring systemic treatment (such as disease-modifying drugs, corticosteroids, or immunosuppressants) have occurred within 2 years prior to the first dose of the study medication. Replacement therapies (such as thyroid hormone, insulin, or physiological glucocorticoids for adrenal or pituitary insufficiency, etc.) are not considered systemic treatment; 5. Receiving systemic corticosteroid treatment (excluding nasal, inhalation, or other local routes of administration) or any other form of immunosuppressive therapy within 7 days prior to the first dose of the study medication; Note: The use of physiological doses of corticosteroids (equivalent to ≤50 mg\u002Fday of hydrocortisone or equivalent) is permitted; 6. The subject has been using traditional Chinese medicine or other immunomodulators within 2 weeks prior to enrollment; 7. Symptomatic ascites or pleural effusion that cannot be controlled with medication and requires therapeutic puncture or drainage; 8. Uncontrolled cardiac clinical symptoms or diseases, such as:\n\n  1. Heart failure at NYHA class 2 or above;\n  2. Unstable angina;\n  3. Myocardial infarction within the past year;\n  4. Clinically significant supraventricular or ventricular arrhythmias requiring treatment or intervention; 9. Known history of abuse of psychiatric drugs, alcoholism, or drug addiction in the subject; 10. Pregnant or nursing women; 11. Men or women of childbearing potential (referring to men or women who have not undergone sterilization surgery, as well as women who have not reached menopause) must use highly effective contraceptive methods (such as oral contraceptives, intrauterine devices, abstinence, or barrier contraception combined with spermicides) during the trial and continue to use contraceptives for 6 months after the last dose; 12. The investigator deems that the subject should be excluded from this study, for example, if the investigator judges that the subject has other factors that may force the study to be terminated prematurely, such as other serious diseases (including psychiatric diseases) requiring concurrent treatment, severe laboratory test abnormalities, or family or social factors that may affect the subject's safety or the collection of data and samples.","75 Years",{"count":50,"type":20},30,[23],"Introduction:\n\nThis document explains a clinical research study conducted at Peking Union Medical College Hospital. The study aims to evaluate a new combination treatment - Envafolimab (an immunotherapy) and Axitinib (a targeted therapy) - for patients newly diagnosed with advanced kidney cancer (specifically, clear cell Renal Cell Carcinoma or RCC). This information is designed to help patients, their families, and healthcare providers understand the study's purpose, procedures, potential benefits and risks, and what participation involves.\n\n1. What is the Study About?\n\n   * The Problem: Advanced kidney cancer (RCC) that has spread (metastatic) or cannot be removed by surgery (unresectable) is challenging to treat. While treatments exist, researchers are always looking for more effective and manageable options, especially for patients who haven't had prior systemic (whole-body) anti-cancer therapy.\n   * The New Approach: This study combines two types of drugs:\n\n     * Envafolimab: An \"immunotherapy\" drug given as an injection under the skin (subcutaneous). It works by blocking a protein called PD-L1 on cancer cells or immune cells. Blocking PD-L1 helps the patient's own immune system recognize and attack the cancer cells more effectively.\n     * Axitinib: A \"targeted therapy\" drug taken as a pill twice daily. It works by blocking signals (VEGF receptors) that cancer cells use to grow new blood vessels, essentially starving the tumor of its blood supply.\n   * The Goal: To find out if giving Envafolimab and Axitinib together is safe and effective as the first treatment for patients with advanced kidney cancer. Researchers want to see how well the combination shrinks tumors, controls the cancer, and how long patients live without their cancer getting worse, while carefully monitoring side effects.\n   * Study Design:\n\n     * Phase II: This is an early stage of testing in patients, focusing mainly on how well the treatment works and its safety profile in a specific group.\n     * Single-Arm: All participants in this study will receive the same combination treatment (Envafolimab + Axitinib). There is no separate group receiving a different treatment or placebo for comparison in this particular study.\n     * Single-Center: Currently being run at Peking Union Medical College Hospital (but could potentially expand).\n     * Participants: Plans to enroll about 30 patients.\n     * Treatment Duration: Patients receive treatment as long as it's working (tumor isn't growing) and they can tolerate the side effects, for up to a maximum of 2 years.\n2. Key Information for Patients \\& Families:\n\n   * Who Might Qualify? You may be eligible to participate if you:\n\n     * Are between 18 and 75 years old.\n     * Have been diagnosed with advanced clear cell kidney cancer (unresectable or metastatic).\n     * Have NOT received any prior systemic anti-cancer treatment (like chemotherapy, immunotherapy, or other targeted therapies) for your advanced kidney cancer.\n     * Have tumors that can be measured on scans (CT or MRI).\n     * Are relatively active and able to care for yourself (ECOG performance status 0 or 1: meaning you are either fully active or restricted in physically strenuous activity but ambulatory and able to do light work).\n     * Have adequate organ function (healthy enough bone marrow, liver, kidneys, heart) as determined by blood tests.\n     * Are expected to live at least 6 more months.\n     * Understand the study and agree to follow the procedures and attend all visits.\n   * Who Would Not Qualify? You would likely not be eligible if you:\n\n     * Have another active cancer besides the kidney cancer being studied.\n     * Have had previous systemic treatment for your advanced kidney cancer.\n     * Have known severe allergies to similar drugs or components of Envafolimab\u002FAxitinib.\n     * Have an active autoimmune disease needing strong medication (like high-dose steroids or immunosuppressants) within the last 2 years. (Hormone replacements like thyroid meds are okay).\n     * Are taking high-dose steroids (except inhaled\u002Fnasal) or other immune-suppressing drugs shortly before starting.\n     * Are using traditional Chinese medicine or immunomodulators within 2 weeks before joining.\n     * Have serious uncontrolled heart problems (like recent heart attack, severe heart failure, unstable angina, significant irregular heartbeats).\n     * Have uncontrolled fluid build-up needing drainage (like large amounts of ascites or pleural effusion).\n     * Are pregnant, breastfeeding, or unwilling to use highly effective contraception during the study and for 6 months after.\n     * Have significant psychiatric, substance abuse, or other medical\u002Fsocial issues that the research team believes would interfere with the study.",[26],"NOT_YET_RECRUITING","2025-08-28",{"date":57,"type":33},"2025-09-08",{"date":59,"type":20},"2025-09-01",{"date":61,"type":20},"2027-07-20",{"name":63,"class":40},"Peking Union Medical College Hospital"]