Nexien BioPharma (QB) Stock Price

0.00 (0.0%)
Volume 55
Bid Price 0.0257
Ask Price 0.05
News -
Day High


52 Week Range


Day Low
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Company Name Stock Ticker Symbol Market Type
Nexien BioPharma Inc (QB) NXEN OTCMarkets Common Stock
  Price Change Change Percent Stock Price Last Traded
0.00 0.0% 0.0599 16:30:13
Open Price Low Price High Price Close Price Prev Close
0.0599 0.0599
Trades Volume Avg Volume 52 Week Range
2 55 - 0.0302 - 0.2585
Last Trade Time Type Quantity Stock Price Currency
12:34:13 32 $ 0.0478 USD


Draw Mode:

Nexien BioPharma Inc (QB) Financials

Market Cap Shares in Issue Float Revenue Profit/Loss EPS PE Ratio
$ 3.34M 55.77M 11.23M $ - $ - - -
Short Interest Dividends Per Share Dividend Yield Ex-Div Date Insider B/S Insider % Owned
2.45k $ - - - -

more financials information »

Nexien BioPharma (QB) News

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Historical NXEN Price Data

Period Open High Low VWAP Avg. Daily Vol Change %
1 Week0.06020.072550.03020.043782639,717-0.0003-0.5%
1 Month0.06530.08490.03020.055827521,589-0.0054-8.27%
3 Months0.0750.09990.03020.068097315,120-0.0151-20.13%
6 Months0.0860.1230.03020.074062814,627-0.0261-30.35%
1 Year0.1090.25850.03020.114233523,103-0.0491-45.05%
3 Years0.170.4450.00850.128616335,630-0.1101-64.76%
5 Years1.206.000.00850.184311332,876-1.14-95.01%

Nexien BioPharma (QB) Description

Nexien BioPharma Inc. is a US-based pharmaceutical company engaged in the formulation, development and commercialization of cannabinoid-based pharmaceuticals, in accordance with U.S. Food and Drug Administration ('FDA') pre-clinical and clinical pathways, to address a broad range of medical conditions and disorders. Nexien BioPharma's drug development strategy consists of: A. The determination of medical conditions and disorders that could potentially benefit from cannabinoid-based formulations; B. Conducting "freedom to operate" investigations on these conditions; C. The preparation of patent applications and the prosecution of such application and/or the licensing of existing patents; D. Identifying the regulatory pathway with the FDA; and E. Proceeding with pre-clinical and clinical development activities in accordance with FDA protocols for submission to obtain approval for the particular product(s).

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