Target- |
MechanismInflammation mediators stimulants |
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Inactive Indication- |
Drug Highest PhaseApproved |
First Approval Ctry. / Loc.US |
First Approval Date24 Dec 1997 |
一项Ⅲ期、随机、单盲、安慰剂对照平行分组临床试验评估滑石粉治疗恶性胸腔积液的有效性及安全性
[Translation] A phase III, randomized, single-blind, placebo-controlled, parallel-group clinical trial to evaluate the efficacy and safety of talc in the treatment of malignant pleural effusion
[Translation] To explore the effectiveness and safety of talcum powder in the treatment of malignant pleural effusion
/ RecruitingNot ApplicableIIT Evaluation of the Performance and Tolerance of the NOVATECH ® LUCIOLA TM EB Fiducial Marker During Radiotherapy Sessions in Patients Suffering From Lung Cancer: Multicenter, Post CE-mark Study
Following CE certification, this Post Market Clinical Follow-up investigates the performance and safety of using the new fiducial marker, NOVATECH® LUCIOLA™ EB, in the lung airways to monitor in real-time tumor location during radiotherapy.
At the time of insertion near the tumor, the Luciola's 3 fiducial marker arms are deployed simultaneously. Optimal detection of the fiducial marker is considered during the radiotherapy treatment.
100 Clinical Results associated with Novatech SA
0 Patents (Medical) associated with Novatech SA
100 Deals associated with Novatech SA
100 Translational Medicine associated with Novatech SA