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Sirona Biochem Corp V.SBM

Alternate Symbol(s):  SRBCF

Sirona Biochem Corp. is a cosmetic ingredient and drug discovery company with a proprietary technology platform developed at its laboratory facility in France with a specialization in the stabilization of carbohydrate molecules. The Company is exploring the areas of diabetes, dyschromia, anti-aging, anti-cellulite and antiviral therapies and relies on a business model of licensing patents to large organizations in return for up-front and milestone payments as well as royalties. Its two most advanced programs are the cosmetic skin lightener and diabetes drug. The Company's TFC-1067 is for the treatment of Dyschromia (Dark spots on the skin). GlycoProteMim is a novel anti-aging compound. GlycoProteMim is based on the naturally occurring glycoproteins found in Antarctic fish, known to protect them against environmental stressors. It is focused on three current antiviral categories: Neuraminidase Inhibitors, Nucleoside Analogs and Iminosugars. Its wholly owned subsidiary is TFChem S.A.R.L.


TSXV:SBM - Post by User

Comment by 24minus7on Jun 25, 2023 11:16am
143 Views
Post# 35513541

RE:RE:Trenibrorher@w:o - Novartis&Sirona?!

RE:RE:Trenibrorher@w:o - Novartis&Sirona?!
Trenibrother also seems to have a simple explanation for this:
 
It is quite simple:
Company A is interested in an active ingredient of company B. Now, it is not unusual in the pharmaceutical industry to record possible contract negotiations intended at a later point in time, for example in a LOI (letter of interest).
Furthermore, confidentiality, due diligence, etc. can be agreed here. However, an LOI is not subject to notification.
In the case of Company B's substance, however, it is still in development and a certain efficacy has not been researched at all at the time of the interest and is therefore anything but proven. In the case of TFC-039, we are talking about a completed phase 1 trial by Wangbang with correspondingly available data material.
Company A may consider the existing data material to be promising and agree an LOI (letter of intent) with company B, of which we know nothing.
Company A is not at all able to assess the benefit and possible success at the current stage of development and carries out due diligence (DD). This includes, among other things, clinical studies, in this case phase 2 and phase 3 studies, which is why such a DD can sometimes take a long time.
 
So everything is possible and legal.
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