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Lexaria Bioscience Corp LEXX

Alternate Symbol(s):  LEXXW

Lexaria Bioscience Corp. is a Canada-based biotechnology company. The Company is engaged in pursuing the enhancement of the bioavailability of a diverse and a range of active pharmaceutical ingredients (API) using DehydraTECH, its patented proprietary drug delivery technology. The Company’s patented drug delivery technology, DehydraTECH, is designed to improve the way active molecules enter the bloodstream upon oral ingestion. DehydraTECH has also demonstrated enhanced delivery of certain active molecules into brain tissue. The Company has also developed DehydraTECH formulations for other applications demonstrating bio-absorption when administered intraorally and topically. It operates through two segments: Intellectual Property and Products. It also operates a licensed in-house research laboratory and holds an intellectual property portfolio with 35 patents granted and many patents pending worldwide. Its subsidiaries include Lexaria CanPharm ULC, and Lexaria CanPharm Holdings Corp.


NDAQ:LEXX - Post by User

Post by SkyLight8on Nov 23, 2021 9:02am
441 Views
Post# 34156276

IND a shooo in if we can sustain only 10% drop

IND a shooo in if we can sustain only 10% drop Even if we treat the mild untreated population as a preventitive to worsening heart disease 

1 billion cap easy on major deal with $JAZZ and we sit back and relax while they spend all phases

IND is the Next Step on the Road to an NDA for DehydraTECH - CBD

Armed with the most recent test results and a history of success with DehydraTECH technology, Lexaria Bioscience Corp (NASDAQ: LEXX) announced last week that it has formally begun the process for an Investigational New Drug application filing with the FDA. The application will list DehydraTECH CBD as a prospective registered pharmaceutical treatment for hypertension.

This is another step to an eventual NDA, provided that ongoing studies continue to show positive results and the company doesn't run into any regulatory hurdles. With both internal and external data on the effectiveness of DehydraTECH, the company may be able to file using the abbreviated 505(b)(2) NDA application, which could significantly speed up timelines.

FDA approval for CBD pharmaceutical treatments is not unprecedented. In 2018, the FDA approved Epidiolex®, a CBD-based pediatric anti-seizure medication. The approved dosage rate for a child weighing 28kg was 140mg, with an increase to 280mg daily for long-term use. DehydraTECH CBD dosages, due to its absorption capabilities, could be significantly less.

DehydraTECH Could Rise to Mega-Drug Status in the BP Space

"If we can sustain these results, we could be looking at mega-drug status ($1 billion per year) in the hypertension market," stated Chris Bunka when asked about projections for the future. "Our goal now is to put together a 4-week study, three doses per day, targeting a sustained drop in blood pressure. That could make us one of the most effective registered pharmaceutical treatments for hypertension in the world, with few if any unwanted side effects."

The process ahead will still take several months, but shareholder optimism is high as DehydraTECH CBD continues to be proven effective in multiple applications. Lexaria's commercial success with their technology has already been established. A pharmaceutical breakthrough in the anti-hypertensive space could launch them into unicorn status.

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