• For Acyclovir Lauriad®, the Company has engaged discussion with European regulatory agencies and obtained a registration slot. While standard drug development usually requests a second phase III trial prior to file for market authorization, BioAlliance Pharma has initiated promising discussion with European and US agencies to recognize Acyclovir Lauriad® clinical benefits and allow a much shorter process.
  • S1 2010 record turnover with €21.3 M versus €4.1 M for the same period in 2009. BioAlliance has again shown the capacity to reach on time important milestones, including its new European partnership with Therabel (March 2010), followed by the FDA approval of Loramyc®/ Oravig® (April 2010).


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Life Science Career Day 201816.05.2018

Wednesday 16 May 2018 @ CHUV 350 participants have already registered to LSCD18: you have until April 20th to join...

EspeRare gains rights to relaunch late stage development for a rare genetic disease

EspeRare is delighted to announce that it has concluded an important agreement with Edimer Pharmaceuticals.
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