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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 proprietary platform developed at its laboratory facility in France. Through its wholly owned subsidiary TFChem S.A.R.L., the Company specializes in stabilizing carbohydrate molecules. The principal activities of the Company include development of cosmetic and pharmaceutical active ingredients. TFChem develops and markets its GlycoMim technology for pharmaceutical and biotechnology comp anies. TFChem’s proprietary chemistry technology can be applied to the development of several pharmaceutical domains such as cancer, diabetes, pain and inflammation and cardio-vascular diseases. Its cosmetic therapeutic area includes skincare-dark spot corrector (Rx & OTC), cell preservation and repair (including keloid and scar therapy), skincare-anti aging/anti-wrinkle and skincare-cellulite treatment. It has developed an active ingredient, TFC-1067 for the treatment of Dyschromia (Dark spots on the skin).


TSXV:SBM - Post by User

Bullboard Posts
Comment by malibukion Dec 29, 2017 4:43pm
63 Views
Post# 27248422

RE:RE:Dapaglifizin from AZ

RE:RE:Dapaglifizin from AZWex in preclinical you have certain off-targets that you want to avoid for hearth failure etc cases especially. By previouss sglt2 drugs it is shown that inhibiting sglt2 (assuming that drug is not chemically super different from Sirona's) is Ok. The issue is toxicity due to its function, urinary track infections etc as MWM pointed out. May be drug will work for diabetes but also increase UT infections would you still approve? This will depend on data and no one can comment on that before ph 1 (better ph 2) data min a year or two. It is not risk free that is why I said normally less than 10% chance but in this case may be 30%.

For possible tox (source not academic but fine)

https://www.medicinenet.com/sglt2_inhibitors_type_2_diabetes_drug_class/article.htm

Serious side effects of SGLT2 inhibitors include:

MWM also ponted about amputation risk which is recently included
https://www.diabetesincontrol.com/uncommon-side-effect-amputation-risk-with-canagliflozin/
For 1067 trial even if such test would take short time (4 to 8 weeks) the whole regulatory process is not short and could take 6 months to a year. See the cases
https://clinicaltrials.gov/ct2/show/NCT01016080
https://clinicaltrials.gov/ct2/show/NCT01249469
Bullboard Posts