ATHENA

1. Bilastine is a potent, effective antihistamine, without sedation, without cardiac toxicity, it has absence of metabolism and does not interact with cytochrome P4502.2. In experimental models, Bilastine has shown an excellent dose-dependent activity when administered by oral or intravenous rout...

Selective D2/D3 dopamine antagonist.n Combine prokinetic and anti-emetic activities on gastrointestinal tract making it an ideal agent for treating gastroparesis (postprandial fullness, nausea, vomiting and stomach fullness). Does not cross the blood-brain barrier minimizing CNS adverse events

Lesser behaviour deterioration vs. Galantamine14.n Superior Global Responder Rate vs. Galantamine14.n Lower risk of treatment withdrawals for any reason or because of an adverse event for Donepezil vs. Rivastigmine or Galantamine14

First single stereospecific S-isomer of omeprazole less prone to first-pass metabolism1.n Higher bioavailability than omeprazole2.n Superior acid control compared with all other Proton Pump Inhibitors (omeprazole, pantoprazole, lansoprazole & rabeprazole)3, 4, 

Anxiolytic effect equivalent to lorazepam, a higher responder rate, and a lower rate of rebound anxiety at treatment discontinuation (one week) in patients receiving etifoxine5.

The purpose of this section, is to give to the audience some advice and warnings on how to better develop and produce a customized drug delivery medical device, based on our own experience. in fact the pathway for a new drug delivery medical device, is full of the unexpected and sometimes the company has to stop the development phase so they never get to production or they spend a lot more money and time compared to a better path/arrangement. There will be also examples and case studies taken from our own experience. The other purpose of this section, is to show you the advantages of a customer centric and multidisciplinary approach to develop and produce a customized drug delivery device.