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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

Comment by jdstoxon Jun 10, 2020 1:28pm
221 Views
Post# 31134273

RE:RE:Denali update

RE:RE:Denali updateI really don't want to be here but the DNL747/DNL788 discussion is a little off track.

The Denali study with DLN747 was stopped because Sanofi/Denali needed to increase its clinical dose to achieve better efficacy, but a monkey study showed toxicity at the doses Sanofi/Denali needed. They simply couldn't put higher doses of DLN747 in humans so they stopped the clinical trial.

DLN747 does not need a transporter such as xB3 or Denali's Transport Vehicle (TV) to get across the BBB and into the brain. DLN747 is a small molecule that is small enough to cross the BBB. It is lipid soluble (lipophilic) meaning that it is soluble in fats. It is, therefore, hydrophobic and is not soluble in water.

Small molecules that are water soluble (hydrophilic) generally do not cross the BBB.

DNL747 is being replaced in the Sanofi/Denali pipeline and clinical trials with DNL788, which is also a small molecule with a slightly different molecular structure than DNL747 has. Both drugs attempt to mediate necroptosis, a type of cell death process that occurs with various diseases like MS, ALS and Alzheimer's. You can read more about this and other cell-death processes in this scientific paper from NIH

Long-term readers, if they look at this NIH paper, will note reference to TNF, tumour necrosis factor. I and a couple of others discussed TNF back in 2014/15. At the time there was speculation that TNF was the subject of studies that MedImmune was doing with Bioasis, the speculation being that MedImmune had an antibody that needed delivery across the BBB for dealing with MS, ALS, Alzheimer's or something else related to TNF. We quickly dropped that discussion when it seemed evident that TNF-related treatments being developed may be small molecules and not antibodies. I also learned at that time that MedImmune was using xB3 (MTfp) to deliver an antibody that dealt with pain, but I couldn't discuss that until a little later when it became public knowledge.

So, that's my take on DNL747 story.

On another note, obviously SH hasn't yet shut down "jdstox" as I requested. Responses of this type will occur on my own site as soon as I can make that happen. 

I also want to thank everybody for the incredible outreach to me over the past few days. I will attempt to deliver on a level consistent with your faith in me. Thank you so much. 

jdstox
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