[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100557398":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":26,"centralContacts":27,"locations":37,"responsibleParty":102,"collaborators":26,"id":104,"slug":105,"hasResults":106,"nctId":107,"briefTitle":108,"officialTitle":109,"acronym":110,"eligibilityCriteria":111,"healthyVolunteers":106,"sex":112,"minAge":113,"maxAge":26,"enrollmentInfo":114,"targetDuration":26,"studyType":117,"phases":118,"briefSummary":120,"conditions":121,"keywords":124,"overallStatus":40,"whyStopped":26,"lastUpdateSubmitDate":126,"lastUpdatePostDateStruct":127,"startDateStruct":130,"completionDateStruct":132,"leadSponsor":134,"locationsCount":136},{"fullName":5,"class":6},"Telix Pharmaceuticals (Innovations) Pty Limited","INDUSTRY",[8,14,17],{"label":9,"type":10,"description":11,"interventionNames":12},"Part A","EXPERIMENTAL","One Injection of 89Zr-TLX300-CDx",[13],"Drug: 89Zr-DFOsq-olaratumab (89Zr-TLX300-CDx)",{"label":15,"type":10,"description":11,"interventionNames":16},"Part B",[13],{"label":18,"type":10,"description":11,"interventionNames":19},"Part C",[13],[21],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"DRUG","89Zr-DFOsq-olaratumab (89Zr-TLX300-CDx)","Single administration of 89Zr-TLX300-CDx",[9,15,18],null,[28,33],{"name":29,"role":30,"phone":31,"phoneExt":26,"email":32},"Brenda Cerqueira, M.Sc","CONTACT","+61 83180090","brenda.cerqueira@telixpharma.com",{"name":34,"role":30,"phone":35,"phoneExt":26,"email":36},"Jui Patil","+61 434919406","jui.patil@telixpharma.com",[38,61,82],{"facility":39,"status":40,"city":41,"state":42,"zip":43,"country":44,"countryCode":45,"cosmosGeoPoint":46,"geoPoint":51,"contacts":52},"Princess Alexandra Hospital 199 Ipswich Road, Woolloongabba","RECRUITING","Brisbane","Queensland","4102","Australia","AU",{"type":47,"coordinates":48},"Point",[49,50],153.02809,-27.46794,{"lat":50,"lon":49},[53,57],{"name":54,"role":30,"phone":55,"phoneExt":26,"email":56},"Vladimir Andelkovic","+61731766577","vladimir.andelkovic@health.qld.gov.au",{"name":58,"role":30,"phone":59,"phoneExt":26,"email":60},"Loren Katchel","+617 3176 1810","Loren.Katchel@health.qld.gov.au",{"facility":62,"status":40,"city":63,"state":64,"zip":65,"country":44,"countryCode":45,"cosmosGeoPoint":66,"geoPoint":70,"contacts":71},"Precision Molecular Imaging & Theranostics Pty Ltd","Melbourne","Victoria","3051",{"type":47,"coordinates":67},[68,69],144.96332,-37.814,{"lat":69,"lon":68},[72,76,79],{"name":73,"role":30,"phone":74,"phoneExt":26,"email":75},"Christopher Marinakis, MMedRad, BBSc","+61 3 94545804","cmarinakis@mtic.net.au",{"name":77,"role":30,"phone":74,"phoneExt":26,"email":78},"Jason Callahan","jcallahan@mtic.net.au",{"name":80,"role":81,"phone":26,"phoneExt":26,"email":26},"Rodney Hicks, Prof.","PRINCIPAL_INVESTIGATOR",{"facility":83,"status":84,"city":85,"state":86,"zip":87,"country":44,"countryCode":45,"cosmosGeoPoint":88,"geoPoint":92,"contacts":93},"GenesisCare Murdoch 100 Murdoch Drive, Murdoch WA","NOT_YET_RECRUITING","Perth","Western Australia","6150",{"type":47,"coordinates":89},[90,91],115.8614,-31.95224,{"lat":91,"lon":90},[94,98],{"name":95,"role":30,"phone":96,"phoneExt":26,"email":97},"Aviral Singh","+61893661500","aviral.singh@genesiscare.com",{"name":99,"role":30,"phone":100,"phoneExt":26,"email":101},"Julie Rowe","0498477691","julie.rowe@genesiscare.com",{"type":103,"investigatorFullName":26,"investigatorTitle":26,"investigatorAffiliation":26,"oldNameTitle":26,"oldOrganization":26},"SPONSOR","100557398","phase-1-89zr-olaratumab-dosimetry-in-participants-with-soft-tissue-sarcoma-100557398",false,"NCT06537596","89Zr-olaratumab Dosimetry in Participants With PDGFR Alpha Positive Solid Tumours and Soft Tissue Sarcoma","An Open-label, Phase 1 Study to Assess Safety, Tolerability, Dosimetry, Pharmacokinetics and Imaging Properties of 89Zr-olaratumab (89ZrTLX300-CDx) in Participants With PDGFR Alpha Positive Solid Tumours and Soft Tissue Sarcoma","ZOLAR","INCLUSION CRITERIA:\n\n1. ≥18 years of age at the time of signing the informed consent.\n2. Histologically confirmed diagnosis of soft tissue sarcoma (STS). Patients with indications other than STS, that could be PDGFRα positive, will also be considered This would be subject to case-by-case approval by the Sponsor.\n3. At least one mass of \\> 2cm in largest diameter seen on standard care imaging (CT or MRI) or at least one lesion detected positive via FDG-PET.\n4. Participants must have consented to provide prior\u002Farchival FFPE tumour tissue or biopsy\u002Fresected tissues collected up to 30 days after visit 2 (89Zr-TLX300-CDx administration) - please refer to the Laboratory manual for description of tissue requirements.\n\n   It is preference that biopsies have been collected within 3 months of trial participation (but not mandatory).\n5. Adequate haematologic function as defined by an absolute neutrophil count (ANC) ≥ 1500\u002F μL, haemoglobin ≥ 9.0 g\u002FdL, and a platelet count of 100,000\u002FμL obtained.\n6. Adequate hepatic function as defined by a total bilirubin ≤ 1.5 mg\u002FdL, and aspartate transaminase (AST) and alanine transaminase (ALT) ≤ 3.0 times the upper limit of normal (ULN).\n7. Adequate renal function as defined by serum creatinine ≤ 1.5 × the institutional ULN. If creatinine is above the ULN, the participant's creatinine clearance is ≥ 45 mL\u002Fmin.\n8. Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.\n9. Female participants of childbearing potential must have negative pregnancy tests at screening, as well as confirmation of negative pregnancy test result within 24 hours prior to receiving 89Zr-TLX300-CDx. Female participants of childbearing potential or male participants with female partners of childbearing potential must:\n\n   1. be willing to practice full and true sexual abstinence; or\n   2. be surgically\u002Fpermanently sterile or with a history of hysterectomy for women; or\n   3. be willing to practice highly effective contraception by using: a non-oral, injected or implanted non-oestrogen progesterone based hormonal method, male condom, vaginal diaphragm, cervical cap, intrauterine device, for 3 months after the administration of 89Zr-TLX300-CDx.\n\n11\\. Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.\n\nEXCLUSION CRITERIA:\n\n1. Known or suspected hypersensitivity to olaratumab, DFOsq, 89Zr or any of the excipients.\n2. IgE antibodies against galactose-α-1,3-galactose (α-Gal) above the ULN, \\>0.7 kU\u002FL.\n3. Exposure to any experimental diagnostic or therapeutic drug within 30 days from the date of planned administration of 89Zr-TLX300-CDx.\n4. Surgery ≤ 2 weeks prior to the administration of 89Zr-TLX300-CDx or significant ongoing complications of surgery. Biopsy ≤ 2 weeks prior to the administration of 89Zr-TLX300-CDx is allowed.\n5. Exposure to any radiopharmaceutical within 10 half-lives prior to the administration of 89Zr-TLX300-CDx.\n6. Planned to commence systemic antineoplastic therapies, immunotherapy, targeted therapy, radiotherapy and\u002For surgery for the period between administration of 89Zr-TLX300-CDx and last imaging timepoint, i.e., (Visit 4 for Parts A and B; Visit 5 for Part C). Existing or ongoing therapies may be continued during the imaging window, without washout period.\n7. Serious non-malignant disease (e.g., psychiatric, infectious, autoimmune or metabolic), unresolved serious symptoms from previous therapies, or any disease that may interfere with the objectives of the study or with the safety or compliance of the participant, as judged by the Investigator.\n8. Pregnant or lactating person.\n9. Participants unable to declare meaningful informed consent on their own (e.g., with legal guardian for mental disorders) or unable to tolerate the study procedures.","ALL","18 Years",{"count":115,"type":116},50,"ESTIMATED","INTERVENTIONAL",[119],"PHASE1","Soft Tissue Sarcoma (STS) is a cancer of soft tissues that often expresses Platelet-Derived Growth Factor Receptor (PDGFR)α, a potential therapeutic target. PDGFRα is also found in other advanced solid tumours.\n\nOlaratumab, a PDGFRα-targeted antibody, may be used to deliver radioactive isotopes for imaging or therapy. This first-in-human study will evaluate zirconium-89-labelled olaratumab (⁸⁹Zr-TLX300-CDx) for imaging in patients with STS, selected PDGFRα-positive solid tumours and identification of patients that may benefit from future treatments.",[122,123],"Soft Tissue Sarcoma","PDGFR Alpha Positive Solid Tumours",[122,125],"Solid Tumours","2026-08-12",{"date":128,"type":129},"2026-08-14","ACTUAL",{"date":131,"type":129},"2024-10-31",{"date":133,"type":116},"2027-12",{"name":135,"class":6},"Telix Pharmaceuticals (Innovations) Pty Ltd",3]