Shares of MeiraGTx Holdings PLC (NASDAQ:MGTX – Get Free Report) have received an average rating of “Moderate Buy” from the seven ratings firms that are covering the firm, Marketbeat Ratings reports. One equities research analyst has rated the stock with a sell rating, one has given a hold rating, four have issued a buy rating and one has assigned a strong buy rating to the company. The average 12-month price objective among brokers that have issued a report on the stock in the last year is $26.00.
A number of brokerages recently commented on MGTX. Weiss Ratings reiterated a “sell (d-)” rating on shares of MeiraGTx in a research note on Thursday, January 22nd. Zacks Research upgraded shares of MeiraGTx from a “strong sell” rating to a “hold” rating in a research report on Monday, March 9th. Finally, HC Wainwright assumed coverage on MeiraGTx in a report on Monday, November 24th. They set a “buy” rating and a $20.00 price objective for the company.
Check Out Our Latest Analysis on MGTX
Institutional Trading of MeiraGTx
MeiraGTx Price Performance
NASDAQ:MGTX opened at $7.39 on Monday. MeiraGTx has a one year low of $4.55 and a one year high of $9.73. The company has a market cap of $594.82 million, a P/E ratio of -3.50 and a beta of 1.37. The firm’s fifty day moving average price is $7.57 and its two-hundred day moving average price is $7.94. The company has a debt-to-equity ratio of 26.29, a current ratio of 0.22 and a quick ratio of 0.22.
MeiraGTx Company Profile
MeiraGTx Holdings plc is a clinical-stage biotechnology company dedicated to developing gene therapies for the treatment of rare diseases. Founded in 2014 as an outgrowth of research at University College London, the company focuses on leveraging adeno-associated virus (AAV) vectors to deliver functional genes to target tissues. MeiraGTx’s pipeline spans ocular, central nervous system and systemic indications, addressing conditions such as inherited retinal dystrophies and neurodegenerative disorders that currently lack effective therapies.
The company’s lead programs include AAV-based candidates designed to restore or replace defective genes underlying rare retinal diseases and to modulate cellular pathways in neurological disorders.
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