NXEN

Nexien BioPharma (QB) Stock Price

0.122
0.002 (1.67%)
0.122

Low
0.0085

52 Week Range

High
0.445

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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
0.002 1.67% 0.122 12:00:31
Open Price Low Price High Price Close Price Prev Close
0.1455 0.12 0.1455 0.12
Bid Price Ask Price Spread News
0.11 0.17 0.06 - -
Trades Volume VWAP Dollar Volume Avg Volume 52 Week Range
7 25,223 $ 0.127232 $ 3,209 - 0.0085 - 0.445
Last Trade Time Type Quantity Stock Price Currency
12:11:12 12 $ 0.14 USD

Nexien BioPharma (QB) Financials

Market Cap Shares in Issue Float Revenue Profit/Loss EPS PE Ratio
$ 6.77M 55.52M 11.23M $ - $ - - -
Short Interest Dividends Per Share Dividend Yield Ex-Div Date Insider B/S Insider % Owned
246.00 $ - 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 Week0.14550.1750.110.117777718,007-0.0235-16.15%
1 Month0.19960.19980.10110.1413948,819-0.0776-38.88%
3 Months0.1510.25850.0810.163915131,173-0.029-19.21%
6 Months0.05830.25850.0280.111296638,3370.0637109.26%
1 Year0.05690.4450.00850.142456569,0340.0651114.41%
3 Years2.994.000.00850.184420440,127-2.87-95.92%
5 Years1.206.000.00850.196767135,807-1.08-89.83%

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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