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Clinical Trials associated with 18F-LNC1007A Phase I Clinical Trial of 18F-LNC1007 Injection PET/CT in Healthy Volunteers and Light Tumor Burden Patients for Evaluating Its Pharmacokinetics, Biodistribution,Dosimetry and Safety
This study is a single-arm, single-center trial aimed at evaluating the pharmacokinetics, bio-distribution, dosimetry, and safety of 18F-LNC1007 injection in healthy volunteers and light tumor burden cancer patients, as defined by <5 lesions on a conventional PET/CT done for clinical purposes and molecular imaging tumor volume of <10ml.
All participants must provide a signed consent form before enrolling in the trial.
For each participant, the study duration will be about 3 weeks including 2 weeks' screening, 1 week of scanning and safety follow-up.
评价18F-LNC1007注射液在中国健康受试者中的药代动力学、生物分布和安全性的I期临床试验
[Translation] A Phase I clinical trial to evaluate the pharmacokinetics, biodistribution and safety of 18F-LNC1007 injection in healthy Chinese subjects
1)评价18F-LNC1007注射液的药代动力学特征;
2)评价18F-LNC1007注射液的生物分布和辐射剂量学;
3)初步评价18F-LNC1007注射液的安全性;
[Translation] 1) Evaluate the pharmacokinetic characteristics of 18F-LNC1007 injection;
2) Evaluate the biodistribution and radiation dosimetry of 18F-LNC1007 injection;
3) Preliminary evaluation of the safety of 18F-LNC1007 injection;
100 Clinical Results associated with 18F-LNC1007
100 Translational Medicine associated with 18F-LNC1007
100 Patents (Medical) associated with 18F-LNC1007
100 Deals associated with 18F-LNC1007