VYNE Therapeutics Inc. (NASDAQ:VYNE – Get Free Report) Director Patrick G. Lepore acquired 15,000 shares of the stock in a transaction dated Wednesday, January 15th. The shares were bought at an average price of $2.92 per share, for a total transaction of $43,800.00. Following the transaction, the director now owns 51,472 shares in the company, valued at approximately $150,298.24. This represents a 41.13 % increase in their position. The acquisition was disclosed in a filing with the Securities & Exchange Commission, which is available at the SEC website.
VYNE Therapeutics Stock Performance
VYNE stock opened at $2.70 on Friday. The firm has a market cap of $39.83 million, a P/E ratio of -3.14 and a beta of 1.30. The firm’s fifty day moving average is $2.96 and its 200 day moving average is $2.35. VYNE Therapeutics Inc. has a 52 week low of $1.57 and a 52 week high of $4.30.
Institutional Inflows and Outflows
A hedge fund recently bought a new stake in VYNE Therapeutics stock. Lynx1 Capital Management LP bought a new stake in shares of VYNE Therapeutics Inc. (NASDAQ:VYNE – Free Report) in the 2nd quarter, according to its most recent 13F filing with the Securities and Exchange Commission. The institutional investor bought 16,194 shares of the company’s stock, valued at approximately $32,000. VYNE Therapeutics accounts for 0.0% of Lynx1 Capital Management LP’s portfolio, making the stock its 17th biggest holding. Lynx1 Capital Management LP owned 0.11% of VYNE Therapeutics as of its most recent filing with the Securities and Exchange Commission. 83.78% of the stock is currently owned by institutional investors.
Analyst Upgrades and Downgrades
Check Out Our Latest Report on VYNE
About VYNE Therapeutics
VYNE Therapeutics Inc, a clinical-stage biopharmaceutical company, focuses on developing proprietary and therapeutics for the treatment of immuno-inflammatory conditions. The company's lead product is VYN201, a locally administered pan- bromodomain and extra-terminal (BET) inhibitor soft drug to address diseases involving multiple, diverse inflammatory cell signaling pathways with low systemic exposure.
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