[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100402553":3},{"organization":4,"armGroups":7,"interventions":26,"overallOfficials":87,"centralContacts":92,"locations":99,"responsibleParty":116,"collaborators":97,"id":118,"slug":119,"hasResults":120,"nctId":121,"briefTitle":122,"officialTitle":123,"acronym":97,"eligibilityCriteria":124,"healthyVolunteers":120,"sex":125,"minAge":126,"maxAge":97,"enrollmentInfo":127,"targetDuration":97,"studyType":130,"phases":131,"briefSummary":133,"conditions":134,"keywords":97,"overallStatus":101,"whyStopped":97,"lastUpdateSubmitDate":140,"lastUpdatePostDateStruct":141,"startDateStruct":144,"completionDateStruct":146,"leadSponsor":148,"locationsCount":149},{"fullName":5,"class":6},"Mayo Clinic","OTHER",[8,18,22],{"label":9,"type":10,"description":11,"interventionNames":12},"Cohort 1 (single treatment MV-s-NAP)","EXPERIMENTAL","Patients receive MV-s-NAP IT on day 1 in the absence of disease progression or unacceptable toxicity. Patients undergo CT scan, MRI, tumor biopsy, and blood and urine sample collection throughout the study.",[13,14,15,16,17],"Biological: Oncolytic Measles Virus Encoding Helicobacter pylori Neutrophil-activating Protein","Procedure: Computed Tomography","Procedure: Magnetic Resonance Imaging","Procedure: Biopsy","Procedure: Biospecimen Collection",{"label":19,"type":10,"description":20,"interventionNames":21},"Cohort 2 (Every 21 day MV-s-NAP)","Patients receive MV-s-NAP IT on day 1 of each cycle. Cycles repeat every 21 days for up to 3 cycles in the absence of disease progression or unacceptable toxicity. Patients undergo CT scan, MRI, tumor biopsy, and blood and urine sample collection throughout the study. (CLOSED TO ACCRUAL 6\u002F9\u002F2025)",[13,14,15,17],{"label":23,"type":10,"description":24,"interventionNames":25},"Cohort 3 (Every 14 day MV-s-NAP)","Patients receive MV-s-NAP IT on day 1 of each cycle. Cycles repeat every 14 days for up to 3 cycles in the absence of disease progression or unacceptable toxicity. Patients undergo CT scan, MRI, tumor biopsy and blood and urine sample collection throughout the study.",[13,14,15,16,17],[27,36,52,72,79],{"type":28,"name":29,"description":30,"armGroupLabels":31,"otherNames":32},"BIOLOGICAL","Oncolytic Measles Virus Encoding Helicobacter pylori Neutrophil-activating Protein","Given IT",[9,19,23],[33,34,35],"MV Encoding NAP","MV-s-NAP","Oncolytic Measles Virus Encoding H. pylori NAP",{"type":37,"name":38,"description":39,"armGroupLabels":40,"otherNames":41},"PROCEDURE","Computed Tomography","Undergo CT scan",[9,19,23],[42,43,44,45,46,47,48,49,50,51],"CAT","CAT scan","Computed Axial Tomography","computerized axial tomography","Computerized axial tomography (procedure)","Computerized Tomography","Computerized Tomography (CT) scan","CT","CT SCAN","tomography",{"type":37,"name":53,"description":54,"armGroupLabels":55,"otherNames":56},"Magnetic Resonance Imaging","Undergo MRI",[9,19,23],[57,58,59,60,61,62,63,64,65,66,67,68,69,70,71],"Magnetic Resonance","Magnetic Resonance Imaging (MRI)","Magnetic resonance imaging (procedure)","Magnetic Resonance Imaging Scan","Magnetic Resonance \u002F Nuclear Magnetic Resonance","Medical Imaging","MR","MRI","MRI Scan","MRIs","NMR Imaging","NMRI","nuclear magnetic resonance imaging","sMRI","Structural MRI",{"type":37,"name":73,"description":74,"armGroupLabels":75,"otherNames":76},"Biopsy","Undergo tumor biopsy",[9,23],[77,78],"BIOPSY_TYPE","Bx",{"type":37,"name":80,"description":81,"armGroupLabels":82,"otherNames":83},"Biospecimen Collection","Undergo blood and urine sample collection",[9,19,23],[84,85,86],"Biological Sample Collection","Biospecimen Collected","Specimen Collection",[88],{"name":89,"affiliation":90,"role":91},"Siddhartha Yadav, MD","Mayo Clinic in Rochester","PRINCIPAL_INVESTIGATOR",[93],{"name":94,"role":95,"phone":96,"phoneExt":97,"email":98},"Clinical Trials Referral Office","CONTACT","855-776-0015",null,"mayocliniccancerstudies@mayo.edu",[100],{"facility":90,"status":101,"city":102,"state":103,"zip":104,"country":105,"countryCode":106,"cosmosGeoPoint":107,"geoPoint":112,"contacts":113},"RECRUITING","Rochester","Minnesota","55905","United States","US",{"type":108,"coordinates":109},"Point",[110,111],-92.4699,44.02163,{"lat":111,"lon":110},[114,115],{"name":94,"role":95,"phone":96,"phoneExt":97,"email":98},{"name":89,"role":91,"phone":97,"phoneExt":97,"email":97},{"type":117,"investigatorFullName":97,"investigatorTitle":97,"investigatorAffiliation":97,"oldNameTitle":97,"oldOrganization":97},"SPONSOR","100402553","phase-1-a-vaccine-mv-s-nap-for-the-treatment-of-patients-with-invasive-metastatic-breast-cancer-100402553",false,"NCT04521764","A Vaccine (MV-s-NAP) for the Treatment of Patients With Invasive Metastatic Breast Cancer","Phase I Trial of Intratumoral Administration of a Measles Virus Derivative Expressing the Helicobacter Pylori Neutrophil-Activating Protein (NAP) (MV-s-NAP) in Patients With Metastatic Breast Cancer","Inclusion Criteria:\n\n* Age \\>= 18 years\n* COHORT 1 ONLY: Pathologically confirmed invasive breast adenocarcinoma with documented estrogen receptor (ER)\u002Fprogesterone receptor (PR) \u002FHER2 status and radiographic evidence of distant metastatic disease\n* COHORTS 2 \\& 3 ONLY: Pathologically confirmed invasive breast adenocarcinoma with documented ER\u002FPR\u002FHER2 status and radiographic evidence of distant metastatic or recurrent disease\n* COHORT 1 ONLY: Radiographic evidence of distant metastatic disease (using 7th edition American Joint Committee on Cancer \\[AJCC\\] criteria) with two discrete sites of measurable disease\n* COHORTS 2 \\& 3 ONLY: Radiographic evidence of distant metastatic or recurrent disease (using 8th edition AJCC criteria) with at least one site of measurable disease\n* Prior therapies:\n\n  * Patients with ER\u002FPR positive, HER2 negative breast cancer must have progressed through at least one prior cytotoxic regimen for advanced disease and no longer be candidates for standard endocrine therapy or combination of endocrine therapy with other agents such as CDK4\u002F6 inhibitors\n  * Patients with HER2 positive breast cancer irrespective of ER\u002FPR status must have received or no longer be candidates for HER2 directed therapy with trastuzumab or pertuzumab\n  * Patients with ER\u002FPR\u002FHER2 negative breast cancer must have progressed through at least one prior cytotoxic regimen for advanced disease\n* COHORT 1: At least one site of recurrent\u002Fmetastatic disease that measures \\> 1 cm in greatest dimension (\\> 2 cm for lung lesions) and is amenable to safe percutaneous intratumoral administration of MV-s-NAP as determined by an interventional radiologist\n* COHORTS 2 \\& 3 ONLY: At least 1 site of recurrent\u002Fmetastatic disease measuring \\> 1 cm in greatest dimension \\[\\> 2 cm for lung lesions\\] (Note that if the lesion injected in cycle 1 is not amenable to re-injection, another lesion could be selected for injection\n* Absolute neutrophil count (ANC) \\>= 1500\u002FuL (=\\\u003C 7 days prior to registration)\n* Platelets (PLT \\>= 100,000\u002FuL) (=\\\u003C 7 days prior to registration)\n* Total bilirubin =\\\u003C institutional upper limit of normal (=\\\u003C 7 days prior to registration)\n* Aspartate aminotransferase (AST) =\\\u003C 2 x upper limit of normal (ULN) (=\\\u003C 7 days prior to registration)\n* Creatinine =\\\u003C 1.5 x ULN (=\\\u003C 7 days prior to registration)\n* Hemoglobin \\>= 9.0 g\u002FdL (=\\\u003C 7 days prior to registration)\n* Negative pregnancy test done =\\\u003C 7 days prior to registration (for women of childbearing potential only)\n* Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1 or 2\n* Ability to provide informed written consent\n* Willingness to return to the Mayo Clinic enrolling institution for follow-up\n* Willingness to provide biologic samples for correlative research purposes\n* Life expectancy \\>= 12 weeks\n* Concomitant administration of a bone modifying agent (e.g., zoledronic acid or denosumab) is permitted for the prevention or management of skeletal related events in patients with bone metastases and documentation of tolerability with prior exposures\n\nExclusion Criteria:\n\n* Known standard therapy for the patient's disease that is potentially curative or definitely capable of extending life expectancy\n* Clinical or radiographic suspicion of impending visceral crisis due to invasion or compression by tumor\n* Active infection =\\\u003C 5 days prior to registration\n* History of other malignancy =\\\u003C 5 years except for non-melanoma skin cancer or carcinoma in situ of the cervix\n* Any of the following prior therapies:\n\n  * Chemotherapy =\\\u003C 3 weeks prior to registration\n  * Immunotherapy =\\\u003C 4 weeks prior to registration\n  * HER2 directed therapy =\\\u003C 3 weeks prior to registration\n  * Targeted therapy =\\\u003C 2 weeks prior to registration (e.g., CDK4\u002F6 inhibitors, everolimus)\n  * Investigational agent =\\\u003C 4 weeks prior to registration\n  * Any viral or gene therapy prior to registration\n* Failure to fully recover from acute, reversible effects of prior systemic therapy regardless of interval since last treatment\n* New York Heart Association classification III or IV, known symptomatic coronary artery disease, or symptoms of coronary artery disease on systems review, or known cardiac arrhythmias (atrial fibrillation or supraventricular tachycardia \\[SVT\\])\n* Untreated or progressive central nervous system (CNS) metastases\n\n  * NOTE: Patients with a history of treated brain metastases (surgical resection, whole brain radiation, and\u002For stereotactic radiosurgery) are eligible only if they are asymptomatic and have stable MRI scans for 3 consecutive months, including \\\u003C 28 days of study entry\n* Standing requirement for blood product support\n* Human immunodeficiency virus (HIV) positive test result or history of other immunodeficiency\n* History of organ transplantation\n* History of chronic hepatitis B or C\n* Other concurrent chemotherapy, immunotherapy, radiotherapy, or any ancillary therapy considered investigational (utilized for a non-Food and Drug Administration \\[FDA\\]-approved indication and in the context of a research investigation)\n* Any concurrent medications that the principal investigator determines could interfere with the trial\n* Treatment with oral\u002Fsystemic corticosteroids, with the exception of topical or inhaled steroids\n* Exposure to household contacts =\\\u003C 15 months old or household contact with known immunodeficiency\n* Allergy to measles vaccine or history of severe reaction to prior measles vaccination\n* History of receiving the measles vaccination with the \"killed vaccine\" between 1963-1967 without subsequent re-immunization (2 doses) with the active, live vaccination.\"","ALL","18 Years",{"count":128,"type":129},54,"ESTIMATED","INTERVENTIONAL",[132],"PHASE1","This phase I trial investigates the side effects and best dose of using a modified measles virus, MV-s-NAP, in treating patients with invasive breast cancer that has spread to other places in the body (metastatic). Both the unmodified vaccination measles virus (MV-Edm) and this modified virus (MV-s-NAP) have been shown to multiply in and destroy breast cancer cells in the test tube and in research mice. MV-s-NAP has been altered by having an extra gene (piece of deoxyribonucleic acid \\[DNA\\]) so that virus can make a protein called helicobacter pylori neutrophil activating protein (NAP) which is normally expressed in inflammatory reactions. Monitoring blood, urine, tissue, and throat swab samples, and using imaging tests may help to determine whether MV-s-NAP has any impact on the amount of disease present in metastatic breast cancer patients.",[135,136,137,138,139],"Anatomic Stage IV Breast Cancer AJCC v8","Invasive Breast Carcinoma","Metastatic Breast Adenocarcinoma","Recurrent Breast Carcinoma","Stage IV Breast Cancer AJCC v6 and v7","2026-06-16",{"date":142,"type":143},"2026-06-17","ACTUAL",{"date":145,"type":143},"2020-09-23",{"date":147,"type":129},"2027-08-15",{"name":5,"class":6},1]