3 results
Approved WMOCompleted
To evaluate the safety, tolerability and pharmacokinetics of ascending single and multiple doses of CH-4051.
Approved WMOPending
The objective of the International Hernia Mesh Registry is to observe a minimum of 3,500 patients for up to 2 years post implantation, in a post-market setting, following the use of either ETHICON Mesh Products or other marketed mesh products to…
Approved WMORecruiting
Main study:Primary:Efficacy:- To assess the clinical outcome at 30 days follow-up after administration of a single subcutaneous injection of zalunfiban versusplacebo in STEMI subjects in the pre-hospital setting.Safety:- To assess bleeding events (…