Nexien BioPharma (QB) Stock Price - NXEN

0.01575
0.00 (0.0%)
0.01575
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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 Low Price High Price Open Price Close Price Last Traded
0.00 0.0% 0.01575 0.00 0.00 0.00 0.01575 09:33:50
Bid Price Ask Price Spread Spread % News
0.0115 0.015 0.0035 23.33% - -
Last Trade Time Type Quantity Stock Price Currency
- 0 $ 0.01575 USD

Nexien BioPharma (QB) Financials

Market Cap Shares in Issue Float Revenue Profit/Loss EPS PE Ratio
$ 850.25k 53.98M 9.67M $ - $ - - -
Short Interest Dividends Per Share Dividend Yield Ex-Div Date Insider B/S Insider % Owned
7.06k $ - 0.00% - -

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 Week0.01170.01950.01170.0142494107,0730.0040534.62%
1 Month0.05360.05890.01080.022655939,631-0.03785-70.62%
3 Months0.040.0740.01080.025774419,384-0.02425-60.63%
6 Months0.07410.07410.01080.032089412,014-0.05835-78.74%
1 Year0.0650.100.01080.04667219,675-0.04925-75.77%
3 Years1.206.000.01080.284834819,034-1.18-98.69%
5 Years1.206.000.01080.284834819,034-1.18-98.69%

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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