8 September 2004 / Öresundshuset / Copenhagen
The first formulated trial product - quick fix or strategic decision?
For the first preclinical trials of a project conducted in an emerging pharma or biotech company, little attention is paid to the formulation. For good reasons, the simplest possible formulation may be chosen, or perhaps the whole issue is left to a CRO to decide upon.
However, eventually there will come a time when the choice of formulation will have a significant effect not just on the outcome of a trial, but also on the subsequent conclusions and decisions for the continued project. "Would the bioavailability have been acceptable with another formulation?", is a question you would rather avoid after completing your first human trial. On the other hand, there may also be cases where it is advisable not to include advanced formulation science in your product at an early stage, as it may repel potential licensees at a later stage.
These and other, related issues are treated in the presentation, which will also present a brief inventory over regional service or technology providers in the field of formulations and drug delivery.
Speaker
Bengt Westrin, Ph.D., Assoc. Prof. Vice President, Business Development from Camurus AB.
Venue
Öresundshuset, Gammel Kongevej 1, third floor, Copenhagen, Denmark.
When?
8 September, 2004
15.30-17.30
Registration fee
MVA members: Free
Non members: 300 DKK
Registration
Anette Andersson, aa@mva.org
Registration deadline 3 September 2004
More information
Anette Andersson, aa@mva.org, +46 46 286 3321 or Stina Gestrelius, sg@mva.org, +46 46 286 33 23.
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