[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100414594":3},{"organization":4,"armGroups":7,"interventions":15,"overallOfficials":31,"centralContacts":35,"locations":41,"responsibleParty":76,"collaborators":39,"id":78,"slug":39,"hasResults":79,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":39,"eligibilityCriteria":83,"healthyVolunteers":79,"sex":84,"minAge":85,"maxAge":39,"enrollmentInfo":86,"targetDuration":39,"studyType":89,"phases":90,"briefSummary":92,"conditions":93,"keywords":100,"overallStatus":44,"whyStopped":39,"lastUpdateSubmitDate":110,"lastUpdatePostDateStruct":111,"startDateStruct":114,"completionDateStruct":116,"leadSponsor":118,"locationsCount":119},{"fullName":5,"class":6},"RasCal Therapeutics, Inc.","INDUSTRY",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"RSC-1255 Treatment","EXPERIMENTAL","Single Arm Study. All study participants receive RSC-1255.",[13,14],"Drug: RSC-1255 Dose Escalation","Drug: RSC-1255 Dose Expansion",[16,24],{"type":17,"name":18,"description":19,"armGroupLabels":20,"otherNames":21},"DRUG","RSC-1255 Dose Escalation","Phase 1a will enroll 40-80 participants to identify the dose limiting toxicity (DLT), recommended Phase 1b dose, and the safety and tolerability of RSC-1255. RSC-1255 is administered orally twice daily, with and without food. Each cycle is 21 days.",[9],[22,23],"Phase 1a","Dose Escalation",{"type":17,"name":25,"description":26,"armGroupLabels":27,"otherNames":28},"RSC-1255 Dose Expansion","Phase 1b will enroll 48-94 participants to further characterize the safety, pharmacology, and clinical efficacy of RSC-1255. RSC-1255 is administered orally twice daily alone or in combination with continuous hydroxychloroquine, with food. Each cycle is 21 days.",[9],[29,30],"Phase 1b","Dose Expansion",[32],{"name":33,"affiliation":5,"role":34},"Michael Mann, MD","STUDY_DIRECTOR",[36],{"name":33,"role":37,"phone":38,"phoneExt":39,"email":40},"CONTACT","310-498-7171",null,"clinicaltrials@rascaltherapeutics.com",[42,56,66],{"facility":43,"status":44,"city":45,"state":46,"zip":47,"country":48,"countryCode":49,"cosmosGeoPoint":50,"geoPoint":55,"contacts":39},"University of California, Los Angeles (UCLA) Department of Medicine - Hematology\u002FOncology","RECRUITING","Los Angeles","California","90404","United States","US",{"type":51,"coordinates":52},"Point",[53,54],-118.24368,34.05223,{"lat":54,"lon":53},{"facility":57,"status":44,"city":58,"state":59,"zip":60,"country":48,"countryCode":49,"cosmosGeoPoint":61,"geoPoint":65,"contacts":39},"Sarah Cannon, SCRI Oncology Partners - Health One","Denver","Colorado","80218",{"type":51,"coordinates":62},[63,64],-104.9847,39.73915,{"lat":64,"lon":63},{"facility":67,"status":44,"city":68,"state":69,"zip":70,"country":48,"countryCode":49,"cosmosGeoPoint":71,"geoPoint":75,"contacts":39},"Sarah Cannon, SCRI Oncology Partners","Nashville","Tennessee","37203",{"type":51,"coordinates":72},[73,74],-86.78444,36.16589,{"lat":74,"lon":73},{"type":77,"investigatorFullName":39,"investigatorTitle":39,"investigatorAffiliation":39,"oldNameTitle":39,"oldOrganization":39},"SPONSOR","100414594",false,"NCT04678648","A Trial of RSC-1255 for Treatment of Patients With Advanced Malignancies","A Phase Ia\u002FIb, Open Label, Multi-center, Non-randomized Dose Escalation and Dose Expansion Study of RSC-1255 Alone or in Combination With Hydroxychloroquine in Patients With Advanced Solid Tumor Malignancies","Inclusion Criteria (Key Factors):\n\n1. Has pathologically confirmed advanced or metastatic malignancy characterized by one or more of the following:\n\n   * Participant is intolerant of existing therapy(ies) known to provide clinical benefit for their condition\n   * Malignancy is refractory to existing therapy(ies) known to potentially provide clinical benefit\n   * Malignancy has progressed on standard therapy\n2. Has evaluable or measurable tumor(s) in dose-escalation by standard radiological and\u002For laboratory assessments as applicable to their malignancy.\n3. Has adequate performance status (PS): Eastern Co-operative Oncology Group (ECOG).\n4. Is age ≥ 18 years.\n5. Has either tissue agnostic tumors and documented RAS mutations or with glioblastoma with or without mutation in RAS\n\nExclusion Criteria (Key Factors):\n\n1. Participants receiving cancer therapy at the time of enrollment.\n2. Any clinically significant disease or condition affecting a major organ system.\n3. Significant cardiovascular disease or electrocardiogram (ECG) abnormalities.\n4. Known Gilbert's disease.\n5. Has had a previous (within 2 years) or has a current malignancy other than the target cancer.\n6. Intermittent hypokalemia\n7. Grade 1 or higher nausea, vomiting, diarrhea at baseline due to underlying disease","ALL","18 Years",{"count":87,"type":88},134,"ESTIMATED","INTERVENTIONAL",[91],"PHASE1","RSC-101 is a Phase 1a\u002F1b clinical trial of RSC-1255 in adult study participants with advanced solid tumor malignancies who are intolerant of existing therapies known to provide clinical benefit, have disease that has progressed after standard therapy, or have previously failed other therapies. The study has two phases. The purpose of Phase 1a (Dose Escalation) is to confirm the appropriate treatment dose and Phase 1b (Dose Expansion) is to characterize the safety and efficacy of RSC-1255.",[94,95,96,97,98,99],"Advanced Malignant Solid Neoplasm","RAS Mutation","Lung Cancer","Colon Cancer","Glioblastoma","Pancreatic Cancer",[101,102,103,104,105,106,98,107,108,109],"Malignancy","Cancer","Refractory","RAS mutation","Lung","Colon","RSC-1255","Progression","Pancreatic","2026-06-22",{"date":112,"type":113},"2026-06-23","ACTUAL",{"date":115,"type":113},"2021-03-03",{"date":117,"type":88},"2027-01-30",{"name":5,"class":6},3]