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Nexien BioPharma (QB) Stock Price

0.00 (0.0%)
Volume 1,161
Bid Price 0.072
Ask Price 0.0915
News (2)
Day High 0.08145


52 Week Range


Day Low 0.08145
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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% 0.08145 16:02:36
Open Price Low Price High Price Close Price Prev Close
0.08145 0.08145 0.08145 0.08145 0.08145
Trades Volume VWAP Dollar Volume Avg Volume 52 Week Range
2 1,161 $ 0.08145 $ 95 - 0.051 - 0.2585
Last Trade Time Type Quantity Stock Price Currency
11:24:37 161 $ 0.08145 USD


Draw Mode:

Nexien BioPharma Inc (QB) Financials

Market Cap Shares in Issue Float Revenue Profit/Loss EPS PE Ratio
$ 4.54M 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 Week0.0730.0870.0730.07313768,9350.0084511.58%
1 Month0.090.09990.070.083412311,729-0.00855-9.5%
3 Months0.09990.1090.0650.082365113,328-0.01845-18.47%
6 Months0.09980.1460.06010.085673216,831-0.01835-18.39%
1 Year0.0650.25850.0510.112444826,9640.0164525.31%
3 Years0.250.4450.00850.136351738,393-0.16855-67.42%
5 Years1.206.000.00850.186804133,260-1.12-93.21%

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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