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biOasis Technologies Ord Shs V.BTI.H

Alternate Symbol(s):  BIOAF

Bioasis Technologies Inc. is a Canada-based biopharmaceutical company focused on research and development of technologies and products intended for the treatment of patients with nervous system, including central nervous system, diseases and disorders. The Company is engaged in the development of its xB 3 platform, which is a peptide-based technology, for the transport of therapeutic agents, in particular biological products, across the blood-brain barrier (BBB). It is focused on both orphan drug indications, including brain cancers, and rare genetic neurodegenerative diseases and neuroinflammatory conditions. The Company is also focused on its Epidermal Growth Factor (EGF) platform for treating rare and orphan neurodegenerative and neuroinflammatory disorders. EGF is a protein that stimulates cell growth and differentiation, notably for myelin producing cells. Its development programs include xB3-001: Brain Metastases, xB3-002: Glioblastoma and xB3-007: Neurodegenerative Disease.


TSXV:BTI.H - Post by User

Post by Sniper007on Jan 25, 2013 4:44pm
209 Views
Post# 20892320

Transcend BT211 and T-DM1 conjugate

Transcend BT211 and T-DM1 conjugate

This article talks about TDM1 delaying progression of HER2 postive breast cancers. This was discussed a while back but thought I would bring it up again. Because BT2111 is 3 times more effective than Herceptin alone and TDM1 targets HER+2 cancer cells, it sounds like a combo conjugate of TDM1 and BT2111 would work exceptionally well but because the treatment costs so much for TDM1 ($188K per year) and would extend the patent life of Herceptin, would Roche want the combo of TDM1 and BT2111? Ie. would the combo be too effective to be ridiculously lucrative? Do they really want to cure/kill HER2 breast cancers completely or would they prefer to simply slow the progression down extracting as much cash as possible?

https://www.fiercebiotech.com/story/t-dm1-results-push-genentechs-armed-antibody-tech-ascos-center-stage/2012-06-03

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