[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100629319":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":25,"centralContacts":31,"locations":37,"responsibleParty":55,"collaborators":25,"id":57,"slug":58,"hasResults":59,"nctId":60,"briefTitle":61,"officialTitle":62,"acronym":25,"eligibilityCriteria":63,"healthyVolunteers":59,"sex":64,"minAge":65,"maxAge":25,"enrollmentInfo":66,"targetDuration":25,"studyType":69,"phases":70,"briefSummary":72,"conditions":73,"keywords":25,"overallStatus":40,"whyStopped":25,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":84},{"fullName":5,"class":6},"Pharmacosmos A\u002FS","INDUSTRY",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Trilaciclib","EXPERIMENTAL","Receives trilaciclib",[13],"Drug: Trilaciclib",{"label":15,"type":16,"description":17,"interventionNames":18},"Placebo","PLACEBO_COMPARATOR","Receives placebo",[19],"Drug: Saline (0.9% NaCl)",[21,26],{"type":22,"name":9,"description":23,"armGroupLabels":24,"otherNames":25},"DRUG","Intravenous infusion",[9],null,{"type":22,"name":27,"description":23,"armGroupLabels":28,"otherNames":29},"Saline (0.9% NaCl)",[15],[30],"dextrose",[32],{"name":33,"role":34,"phone":35,"phoneExt":25,"email":36},"Pharmacosmos A\u002FS Clinical and non-clinical research","CONTACT","+4559485959","info@pharmacosmos.com",[38],{"facility":39,"status":40,"city":41,"state":42,"zip":43,"country":44,"countryCode":45,"cosmosGeoPoint":46,"geoPoint":51,"contacts":52},"Pharmacosmos Investigational Site","RECRUITING","Oakland","California","48073","United States","US",{"type":47,"coordinates":48},"Point",[49,50],-122.2708,37.80437,{"lat":50,"lon":49},[53],{"name":33,"role":34,"phone":54,"phoneExt":25,"email":36},"455-948-5959",{"type":56,"investigatorFullName":25,"investigatorTitle":25,"investigatorAffiliation":25,"oldNameTitle":25,"oldOrganization":25},"SPONSOR","100629319","phase-3-effect-of-trilaciclib-in-the-prevention-of-myelosupression-in-subjects-with-limited-stage-small-cell-lung-cancer-100629319",false,"NCT07473128","Effect of Trilaciclib in the Prevention of Myelosupression in Subjects With Limited-stage Small Cell Lung Cancer","A Phase III, Randomised, Double-blind, Placebo-controlled, Multicentre Trial Comparing Efficacy and Safety of Trilaciclib Versus Placebo in Participants With Limited-stage Small Cell Lung Cancer","Inclusion Criteria:\n\n* Confirmed diagnosis of Limited-Stage Small Cell Lung Cancer\n* Complete recovery from prior anti-tumor surgical procedures\n* Measurable and evaluable disease through tumor assessment\n* Willingness to participate and sign informed consent form\n\nExclusion Criteria:\n\n* Extensive Stage Small Cell Lung Cancer\n* Active cardiovascular disease\n* Known hypersensitivity to trilaciclib, etoposide, carboplatin, cisplatin or any component in their formulations\n* Pregnant or nursing women","ALL","18 Years",{"count":67,"type":68},120,"ESTIMATED","INTERVENTIONAL",[71],"PHASE3","The goal of this clinical trial is to compare the efficacy and safety of trilaciclib versus placebo in subjects with limited stage small cell lung cancer. The main question it aims to answer is:\n\nDoes trilaciclib have a myeloprotective effect in subject with limited stage small cell lung cancer?\n\nParticipants will be randomised to receive either trilaciclib or placebo.",[74],"Limited Stage Small Cell Lung Cancer","2026-06-15",{"date":77,"type":78},"2026-06-17","ACTUAL",{"date":80,"type":68},"2026-06-30",{"date":82,"type":68},"2027-06",{"name":5,"class":6},1]