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Resverlogix Corp T.RVX

Alternate Symbol(s):  RVXCF

Resverlogix Corp. is a Canada-based late-stage biotechnology company. The Company is engaged in epigenetics, with a focus on developing therapies for the benefit of patients with chronic diseases. Its epigenetic therapies are designed to regulate the expression of disease-causing genes. The Company's clinical program is focused on evaluating its lead candidate apabetalone (RVX-208) for the treatment of cardiovascular disease and associated comorbidities, and post-COVID-19 conditions. RVX-208 is a small molecule that is a selective bromodomain and extra-terminal (BET) inhibitor. BET bromodomain inhibition is an epigenetic mechanism that can regulate disease-causing genes. RVX-208 is a BET inhibitor selective for the second bromodomain (BD2) within the BET proteins. It partners with EVERSANA, to support the commercialization of RVX-208 for cardiovascular disease, post-COVID-19 conditions, and pulmonary arterial hypertension in Canada and the United States.


TSX:RVX - Post by User

Bullboard Posts
Comment by princeofcuton Jul 23, 2015 2:20pm
100 Views
Post# 23953569

RE:RE:RE:RE:RE:RE:RE:RE:RE:and meanwhile back in china hepa is still not trading...

RE:RE:RE:RE:RE:RE:RE:RE:RE:and meanwhile back in china hepa is still not trading...four, watch out trussel got banned from the scam board for agreeing with me...re. execution most trials of any size have non-compliance issues and again the failure rests with RVX leadership IMO..

..back to the gong show...IMO it is very "odd" that RVX did a major, major left turn revision in a left turn revisions trial...its like back to PII just with a different primary outcome...and what of all the trashtalking RVX did post PII re. the failure of lipitor-208...very odd and again to me goes to the issue of competence (PS imo the regulators required it to be included)

...re. FDA "approval" for the PIII IMO if RVX don't get formal FDA approval to the PIII it will not get marketing approval...on the too funny list, i am back reviewing earlier expert reports on approval failures in the FDA and this shows up a common cause for failure to gain marketing approval (drug companies who just don't listen to FDA communications)...and Europe and China amount to a hill of beans in comparison to FDA marketing approval.

..on an interesting diversion, do you know of any CDN baby biotechs that were successful with the founder as CEO???? is that list more than 5 if that??? IMO major problems are a) lack of successful regulatory experience (how many therapies have they ever brought to market) b) self-interest, entitlement and enrichment over the company mission and responsibility to shareholders...so for instance, RVX Board guy leaves and starts ESPR (boom nuff said he shoulda been offered anything to become CEO and CoB of RVX i wonder what prevented that)
Bullboard Posts