Found 11 matching trials
Dose Escalation, Safety and Pharmacokinetic Study of AVE8062 Combined With Docetaxel in Patients With Advanced Solid Tumors
PHASE1Primary Objective:
To determine the dose limiting toxicity (DLT), the maxi...
Location
Multiple Locations
AVE8062 in Combination With Platinum-taxane Doublet in Advanced Solid Tumor
PHASE1The purpose of this study is to determine the recommended dose of the combi...
Location
Investigational Site Number 250001
A Study of AVE8062 in Advanced-stage Soft Tissue Sarcoma After Failure of Anthracycline and Ifosfamide Chemotherapies
PHASE3The primary objective of the study is to compare the progression-free survi...
Location
Investigational Site Number 840004
A Study to Investigate the Disposition of Radio-labeled AVE8062 Compound Administered as a 30-minute IV Infusion to Patients With Advanced Solid Tumor
PHASE1Primary Objectives:
* To determine the excretion balance and systemic expo...
Location
Sanofi-Aventis Administrative Office
Dose-escalation, Safety, Pharmacokinetics Study of AVE8062 Combined With Bevacizumab in Patients With Advanced Solid Tumors
PHASE1Primary Objective:
\- To determine the maximum administered dose (MAD) and...
Location
Investigational Site Number 250001
Dose Escalation, Safety and Pharmacokinetic Study of AVE8062 Combined With Cisplatin in Patients With Solid Tumors
PHASE1Primary Objective:
* To determine the maximum tolerated dose based on the ...
Location
Sanofi-Aventis Administrative Office
Study of Ombrabulin in Patients With Platinum-Sensitive Recurrent Ovarian Cancer Treated With Carboplatin/Paclitaxel
PHASE2Primary Objective:
\- To demonstrate an improvement in Progression-Free Su...
Location
Investigational Site Number 840007
Trial of Ombrabulin (AVE8062) in Combination With Taxane and Platinum in Patients With Non-small Cell Lung Cancer
PHASE2Primary Objective:
* To demonstrate progression free survival (PFS) improv...
Location
Investigational Site Number 840001
A Dose-escalation Study of Ombrabulin in Combination With Paclitaxel and Carboplatin in Patients With Advanced Solid Tumors
PHASE1The primary objective of the study is to determine the maximum tolerated do...
Location
Investigational Site Number 392002
Dose Escalation, Safety and Pharmacokinetic Study of AVE8062 in Patients With Solid Tumors
PHASE1Primary objective: To determine the maximum tolerated dose based on the inc...
Location
Sanofi-Aventis Investigational Site Number 392002